2347 Life Sciences Jobs - Page 32

As a Principal Architect - Mernstack, you will collaborate closely with key stakeholders to design and develop a core product for one of our valued clients Your role will require deep technical expertise and a strategic mindset to ensure scalability, performance, and exceptional user experience Responsibilities: - * Lead the architectural design and development of a scalable, high-performance product * Spearhead the modernization of the Radiology Worklist Program s user interface by developing a Micro Frontend (MFE) application using React * Seamlessly integrate the new React-based MFE with existing Angular components, leverage Material-UI (MUI) for a consistent design system * Enhance and refactor backend services built in Node js to support new features, including customizable user-defined worklists * Conduct a comparative analysis of AlloyDB and PostgreSQL to determine the optimal database solution for advanced analytics * Redesign and optimize the database schema to support new functionalities and improve overall system efficiency * Design and implement an intermediate caching layer using Elasticsearch to boost application performance and scalability Experience: - * 15 - 20 Years Educational Qualifications: - * Engineering Degree - BE/ME/ BTech/MTech/ BSc/MSc * Technical certification in multiple technologies is desirable Skills: -Mandatory Technical Skills: - * Node.js, ReactJS, PostgreSQL * strong focus on user experience Good to Have Skills: - * AlloyDB

We are looking for a Senior Analyst to support our analytics and reporting team. Robust analytics and reporting is a priority for our businesses, as the product potential has major implications to a wide range of disciplines. It is essential to have someone who understands and aspires to implement innovative analytics techniques to drive our insights generation across GBU. Key Responsibilities Refresh of existing reports and identify improvement opportunities in reporting and BI tools and as needed structure / functionality with the latest insights as they become available Creation of dashboards to synthesize and visualize key information and enable business decisions Generate insights from the existing dashboards Work to develop industry-leading analytics and reporting capabilities Employ tools, technology, and processes to constantly improve quality and productivity Assist in managing projects efficiently and effectively Processes Lead the delivery of projects in terms of coordination, quality, timeliness, efficiency Quality check of the deliverables of self and peers Adhere to compliance procedures and internal/operational risk controls in accordance with all applicable standards Use latest tools / technologies / methodologies and partner with internal teams to continuously improve data quality and availability by building business processes that support global standardization Stakeholder Engagement Work collaboratively with the stakeholder teams to prioritize work and ensure timely delivery of requests Maintain effective relationships with the end stakeholders within the allocated GBU and tasks, with an end objective to develop reports and analyses as per requirement Collaborate with global stakeholders for project planning and setting up the timelines Technical skills Expert in Relational database technologies and concepts Capable of working on multiple projects simultaneously Hands-on experience of using analytical tools like PowerBI, SQL, Snowflake, advanced Excel (including VBA), etc (Python is good to have) Experience of developing, refreshing and managing dashboards Experience with pharmaceutical datasets (eg IQVIA, Symphony, Komodo, Veeva, Salesforce) An aptitude for problem solving and strategic thinking Ability to synthesize complex information into clear and actionable insights Understanding of pharmaceutical development, manufacturing, supply chain, sales and marketing functions Experience 3-6 years of relevant work experience with solid understanding of principles, standards, and best practices of Pharma Commercial Analytics and Dashboard development. Education Bachelors or Masters degree in areas such as Information Science / Operations / Management / Statistics / Decision Sciences/Engineering/Life Sciences/ Business Analytics or related field. Soft skills Strong learning agility; Ability to manage ambiguous environments, and to adapt to changing needs of the business; Good interpersonal and communication skills; strong presentation skills is a must; Team player who is curious, dynamic, result oriented; Ability to operate effectively in an international matrix environment, with ability to work across time zones; Demonstrated leadership and management in driving innovation and automation leveraging advanced analytical techniques Languages Excellent English communication skills - written and spoken

Design and implement cloud-based integrations using APIs Design and provide subject matter expertise for the development of custom implementations using Java-based solutions, including Vault Java SDK Proficiency in cloud-based DAM architectures (AWS, AZURE, Google Cloud) Develop internal and external tools to help our customers and our consultants. Manage integration and development projects and resources. Creating the framework of technological systems. Plan and design the structure of a technology solution. Communicate system requirements to software development teams. Ability to lead technical discussions and provide clear documentation. Evaluate and select appropriate software or hardware and suggest integration methods. Oversee assigned programs (eg, conduct code review) and provide guidance to team members. Assist with solving technical problems when they arise. Experience in Project Management & Stakeholder Engagement. Ensure the implementation of the agreed architecture and infrastructure. Address technical concerns, ideas, and suggestions. Monitor systems to ensure they meet both user needs and business goals. Desired Profile (Key Skills) 7+ years of experience with integration architecture, design, and development for Content management systems (Veeva, Aprimo, OpenText, SharePoint, Salesforce, etc) Experience with commercial solutions & architecture design & data architecture 8+ years of development experience with one of the following languages: Java, .NET, Python, C#, or C++ Experience building solutions and interfaces in the cloud, SaaS applications using REST APIs and Java SDK Work experience in the Life Sciences. Aptitude for identifying and resolving DAM system issues. Flexibility to adapt to changing DAM requirements and technologies. Good to have Certifications in Adobe AEM, Azure, AWS, Veeva Vault Administration, or DAM-related platforms are a plus.

As Team Lead - Scientific Writing - Omnichannel, within our Hyderabad Hub, you'll be responsible for leading the Scientific Writing domain within the Content Operations Hub, ensuring seamless business continuity and driving strategies aligned with global priorities in Content Operations, GenAI, and digital presence optimization. You will manage resources, budget allocation, and vendor relationships, while overseeing content tagging, metadata management, and utilizing data-driven insights to optimize performance. You will also be responsible for driving synergies between other teams within Omnichannel/GTMC. You will supervise the Scientific Writing team within the Content Operations Hub for planning and executing market-driven campaigns, making data-driven business recommendations, and creating insightful presentations. Main responsibilities: To create synergies and provide functional and operational direction to Scientific Writing team within Content Operations Hub of Omnichannel pillar. Ensure seamless business continuity amidst capability and resource changes within content operations Support the Head/Content Operations Hub Lead for aligning Hub strategy with global business priorities, focusing on Scientific Writing domain within content operations, GenAI and content optimization Lead Scientific Writing team resources to improve individuals skills and enhance Hub services such as content creation, modular content and technical production Support the Head/Content Operations Hub Lead for managing budget allocation and vendor relationships crucial for content production and digital marketing tools Report on content performance metrics and derive actionable insights for senior leadership, ensuring strategic alignment and performance optimization Stay up to date with industry trends and best practices in commercial operations, and standardize all tools/processes used in Omnichannel Scientific Writing domain within activities deployed in hub and ensure their continuous improvement through continuous iteration and external benchmarking approach Support the content transformation program supporting the Glocal co-creation teams Be a strategic advisor for Omnichannel Scientific Writing capabilities execution Have a robust plan and implement concrete moves towards best-in-class capabilities Mentor the team, ensure knowledge sharing across team and company, provide global and local Content Operations teams with best practice and feedback loop on processes People: (1) Lead team of writers in content creation/corresponding support team content enhancement/graphic design/operations team; (2) Coach and develop team on content, process, agile methodologies, thoughtful risk taking, automation & innovation (including GenAI); (3) Maintain effective relationship with the stakeholders within the allocated GTMC pillar and cross-pillars - with an end objective to develop content as per requirement; (4) Interact effectively with health care professionals as relevant; (5) Partner with team to strengthen capabilities and support individual development plans (6) Collaborate with cross-functional teams in GTMC to build digital transformation/to bring innovative digital solutions (7) Provide proactive recommendations on improving scientific content of the deliverables and play an active role to follow the best practices in relation to processes, communications, project management, documentation and technical requirements Performance: (1) Provide strategic support across GTMC pillars; (2) Lead and support development of tools, technology, and processes to constantly improve quality and productivity (3) Ensure Scientific Writing team provides content as per agreed timelines and quality; (4) Coach team to become subject matter, process, and technological experts; and (5) Recommend, lead, and implement tactical process improvements within the department and division-wide Process: (1) Support delivery of projects in terms of resourcing, tools, technology, quality, timeliness, efficiency, and high technical standards for deliveries made by Scientific Writing domain within Content Operations Hub; (2) Contribute to overall quality enhancement by ensuring high scientific standards for the output produced by the Hub; (3) Secure adherence to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards; (4) Facilitate development of complex scientific content (branded/unbranded); (5) Help build talent pool/capabilities/Omnichannel content experts across GBUs/therapeutic area(s); (6) Conduct comprehensive content-need analysis; (7) Implement the content plan and associated activities for the year identified for the pillar; (8) Work with selected vendors within the region to deliver the required deliverables as per defined process; (9) Leverage advanced training delivery tools and techniques thereby enhancing the effectiveness of training delivery; and (10) Design an overall plan of action based on end-user feedback and improve course content and delivery Stakeholder: (1) Work closely with GTMC/Omnichannel pillars (Global, Local, and Hub) to identify content need and assist in developing assigned deliverables and (2) Liaise with Omnichannel/ GBTs/AoR/LexMex to provide relevant and customized deliverables About you Experience : 8-10 years of experience in content creation/optimization (including up to 2 years of experience in leading a diverse team of 5-10 members) in medico-marketing / medical / commercial / Omnichannel domain for the pharmaceutical/healthcare industry/digital platforms; and ability to influence and negotiate Soft and Technical skills : Stakeholder management; proficient in written & oral communication; people management/ability to lead diverse teams; strong organizational and time management skills; and ability to work independently and within a team environment / As applicable (including but not limited to therapeutic area/domain knowledge exposure - Proficient in multiple TAs/domains/GBUs; scientific communications/writing; and/or project management) Education : Advanced degree in life sciences/pharmacy/similar discipline or medical degree Languages : Excellent knowledge of English language (spoken and written) Why choose us Bring the miracles of science to life alongside a supportive, future-focused team Discover endless opportunities to grow your talent and drive your career, whether it s through a promotion or lateral move, at home or internationally Enjoy a thoughtful, we'll-crafted rewards package that recognizes your contribution and amplifies your impact Take good care of yourself and your family, with a wide range of health and we'llbeing benefits including high-quality healthcare, prevention and we'llness programs and at least 14 weeks gender-neutral parental leave Play a key role in shaping and optimizing our content strategy, driving business growth and achieving impactful results

CLIENT ENGAGEMENT: will ensure client satisfaction by maintaining high-quality, proactive communication, understanding and meeting project requirements, and by managing client expectations across projects/engagements, DELIVERY OWNERSHIP: will own and contribute hands-on to project design, planning, and delivery of advisory/research/analytics projects; review the work done by team members; ensure the highest quality standards by actively contributing insightful analysis and presentation of data; help team members acquire new skills and support them in delivering increasingly superior quality work PROJECT OWNERSHIP: will own delivery of consulting and research projects, meet timelines, and manage project risks; will represent project teams in review meetings with clients, REVIEW AND QC: will review work done by analysts and junior consultants; will ensure high quality deliverables by actively contributing through insightful analysis of data, TEAM MENTORSHIP: will be required to drive team members in acquiring new skills and support them in delivering increasingly superior quality work, COLLABORATION: assist the team/ supervisor with specific expertise when required. On a need basis, support BD/sales team with subject matter expertise and help build proposals, etc As part of job responsibilities, you are required to comply with ISO 20252:2019 and ISO 27001 standards. Supervisory Responsibility: Yes Education and Other Requirement: B. Pharm or MSc (Pharma) or Master s degree or in Life Sciences, Pharmacy, or related field. 7 10 years of experience in competitive intelligence, market insights, or strategic analysis within pharma/biotech. Proven leadership or team management experience. In-depth understanding of drug development processes, regulatory pathways, and industry dynamics. Proficient in CI platforms and databases, with strong analytical and synthesis skills. Excellent communication and storytelling skills both written and verbal. Ability to handle ambiguity and drive insights from incomplete or evolving data. Good To Have: Cross-cultural experience of working with teams and clients based in the US/EU Understanding of the US and European market access and pricing environment for prescription drugs. Knowledge, Skill, Ability: Extensive experience in at least one therapy area (Cardiovascular, Immunology, Ophthalmology, Neurology, Oncology, Derma, Gastro, Biosimilars space, any other); should be able to interpret market events and advise clients on business implications of such events on a continued basis, Business acumen: needs to be able to drive revenue growth and profitability by identifying/capturing commercial opportunities, by establishing and articulating value stories in solving client problems, Strong research/consulting skills: proven ability to structure research questions, plan and execute research both qualitative and quantitative and drive strategic insights through in-depth analysis, Client facing experience is a must. Needs to engage clients by developing and delivering compelling engagement structures, reports/ presentations and by leading project/ industry-related conversations, In addition to secondary research skills, hands-on experience in Quantitative Modeling (forecasting, market sizing, other analytics) and Primary Market Research would be highly valuable for this role, High level of proficiency in MS-Office applications PowerPoint and Excel in particular, Familiarity with databases (clinicaltrials.gov, pubmed, IQVIA data, other subscription databases), Needs to be a self-starter. Must own and deliver projects or parts thereof with near-zero supervision; ability to plan and prioritize multiple workstreams to meet timelines is crucial, Qualifications B. Pharm or MSc (Pharma) or Master s degree or in Life Sciences, Pharmacy, or related field

We are hiring performance engineers to expand our investment in performance and scalability. As a performance engineer, you will work closely with many teams across Engineering to evaluate performance, identify performance bottlenecks, and collaborate with engineers to solve performance and scalability issues. The work encompasses: measuring and defining performance baselines, guiding other teams, performing root cause analysis across the entire stack, performing competitive benchmarking, building new workloads, and more. You will have a large impact on shaping the performance of the database. The ideal candidate will have worked with massively complex codebases and possess broad experience in databases, distributed systems, cloud infrastructure, and performance analysis. You Will Increase our performance coverage and understanding of CockroachDB Cloud Develop new workload strategies and methodologies Investigate performance issues Perform competitive benchmarks Guide other teams on benchmarking and performance testing methodologies Build automation tools and frameworks Translate customers workloads to automated performance tests The Expectations In your first 30 days, you will become an integrated member of our engineering team. you'll become familiar with our production systems, software development workflows, and architecture of CockroachDB Cloud. We believe that it s essential for you to take the first month to get to know our technology and our company. you'll be given a starter project to help you learn about a particular area and start to get the lay of the land. After your first month, you will align with the team s development objectives and you will own and complete a medium-sized starter project. Some examples of such projects are performing a large-scale TPC-C benchmark of CockrochDB Cloud , competitive benchmarking or improving our nightly performance test framework- roachperf . By the end of the starter project, you will be a fully-contributing member of the Performance Engineering team. You will also have developed enough familiarity with our engineering processes to propose ,scope and own future projects. You Have Desired experience level ranges from mid to staff level. At a minimum, this role requires: 3+ years of experience as a software engineer writing clean, idiomatic code 2+ years of hands on experience with GCP or AWS Experience with one of the following: Performance Testing, Cloud Infrastructure, Continuous Integration Exceptional communication skills and a collaborative mindset BE/B-Tech in Computer Science or equivalent experience Benefits Medical Insurance Flexible Time Off Paid Holidays Paid Parental Leave Mental we'llbeing Benefits And more!

Attach supplementary materials that support the reports content Check the report is consistent in appearance and adheres to style guidelines Evaluate and adjust user access rights to system documentation to ensure security and validity Launch and manage the review workflow in CMS Receive report approval, final reviewer agreement and initiate approval workflow in CMS/ Veeva Regularly update and maintain records of document ownership and ensure compliance with access protocols Review the report to correct any language or typographical errors About you Experience : Experience in pharmaceutical quality Soft skills : Proficient in problem-solving, attention to detail, and good organizational skills. Ability to work collaboratively with cross-functional teams in a flexible and proactive manner. Strong analytical skills. Agile thinker and learner, adaptable to complex & dynamic environments Technical skills : LIMS, Word, Excel, Power Point; Experience in a Pharmaceutical GxP environment, preferred experience in stability management or activities Education : Bachelors degree in stability science, biology, chemistry, or a related field. Advanced degree preferred Languages : Excellent English communication and writing, French or other Languages in addition preferred

Summary -Provide analytics support to Novartis internal customers (CPOs & Regional marketing and sales teams) on various low-medium complexity analytical reports. -Support and facilitate data enabled decision making for Novartis internal customers by providing and communicating qualitative and quantitative analytics. -Support GBS -GCO business in building practice by involving in various initiatives like knowledge sharing, on-boarding and training support, support team lead in all business related tasks / activities, building process documentation and knowledge repositories -To be an integral part of a comprehensive design team responsible for designing promotional marketing materials. About the Role Key Responsibilities Provide analytics support to Novartis internal customers on various high complexity analytical reports. Working knowledge of multiple datasets e. g. LAAD, Xponent, SMART etc. and managing and organizing data sets from databases to find patterns and trends in data. Transforming these complex and granular data into actionable insights. Putting together specifications to extract/transform data into required formats for different analytical elements using SQL/DSS or other data processing tools. Require experience in quantitative analysis with a demonstrated focus in analytics, and experience with coding languages (SQL OR Python) to query and extract data. Also, experience with BI tools, working with very large data sets is a plus. Create the foundation for more sophisticated approaches to APLD analysis and advanced analytics wherever it is required and beneficial. Establish and maintain positive relationships with key functional stakeholders. Takes initiative to drive standardization of reports across brands. Essential Requirements : Masters/ bachelor s in technology/ life-sciences/ management Minimum of 2 + years experience processing and analyzing real world patient level data (Claims data/EHR etc. , ). Expertise in SQL, DataIKU and/or other data processing tool. Knowledge of Statistical modeling or ML is a plus. Understanding of healthcare terminology and real-world patient level data Good communication and interpersonal skills. Conceptual, analytical & tactical thinking, strategic thought process Desired Requirements : Ability to multi-task, work in a demanding global team environment, work under tight deadlines. Develop and maintain strong individual and team performance. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future together? https://www. novartis. com / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork. novartis. com/network Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

Summary Manager, Payer, Access & Reimbursement play a critical role in supporting the delivery of high-quality, actionable insights for strategic business decisions. This role will be supporting engagement leads in delivering complex analytical solutions using multiple datasets for the IDS team. This role focuses on analysing payer, provider, and patient dynamics to optimize market access analysis, reimbursement, and patient affordability. The candidate should have strong analytical skills, a deep understanding of managed markets/ market access, and the ability to work cross-functionally to drive impactful outcomes. Manager will manage assigned workstreams, drive insight generation, and collaborate closely with both Hyderabad and East Hanover (EH) teams independently to ensure alignment and timely delivery. About the Role Job Description Key Responsibilities Explore, develop, implement, and scale up solutions that address customer needs. Co-create with key stakeholders to build partnerships & collaborations. Collaborating with EH leads to ensure comprehensive market, segmentation, and behavioral analyses are incorporated. Lead, build, and cultivate relationships with stakeholders as part of key account strategic management. Working knowledge of multiple datasets e. g. LAAD, Xponent, Plantrak, SMART etc. and formulary datasets (MMIT, DRG - Fingertip, etc. ), managing and organizing data sets from databases to find patterns and trends in data. Experience in analyzing payer data, formulary coverage, and market share to assess and optimize product access across commercial and government payers. Experience in Segment payers based on their policies, formulary positions, and prescription trends, identifying high-potential accounts and key influencers. Knowledge of predictive analytics and machine learning models to forecast payer behavior, such as formulary changes, policy shifts, or reimbursement trends. Experience in analyzing patient claims data, physician prescribing behavior, and treatment utilization patterns in response to payer policies and formulary changes Monitor competitor activities, including pricing, formulary status, and payer contracts, to assess their impact on market share and market access strategies. Develop scenario-based models to simulate different deals/ contracts and study the impact of different payer policies on product uptake. Provide analytics support to Novartis internal customers on various high complexity analytical reports. Proven Project Management skills for owning the delivery of multiple projects, ensuring delivery of efficient and high-quality work. Work in collaboration with cross-functional teams to improve value and drive process innovation across brands continuously expand horizons through experimentation. Essential Requirements: A proven track record in Market Access (Payer/Formulary/Access), brand performance management, marketing, or a similar role 5+ years of experience in analytics, market access, or decision science, preferably in the pharmaceutical or healthcare sector. Demonstrate the ability to support and implement brand strategies that drive market share and revenue growth. The candidate should be able work in a high performing team fostering a collaborative and innovative mindset. Master s/bachelor s degree in data science, analytics, business, Life Sciences, or a related field. Experience in segmenting payers based on their policies, formulary positions, and prescription trends, identifying high-potential accounts and key influencers. Strong experience in data analysis, insight generation, and project management. Desired Requirements: Demonstrated ability to collaborate across global teams and manage multiple priorities. Excellent communication, presentation, and stakeholder management skills. Experience preparing reports, workshop materials, and executive presentations Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future together? https://www. novartis. com / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork. novartis. com/network Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

Challenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. bms. com/working-with-us . Summary: Responsible for enterprise recipe management and support of the Enterprise Manufacturing Execution Systems (EMES) solution that is utilized across the BMS digital manufacturing network to produce clinical and commercial medicine. The scope of the EMES Recipe Author involves supporting the global strategy for recipe management. This includes developing recipes from the initial requirements phase through to building, testing, and ongoing support. It also encompasses handling PCM necessary to facilitate manufacturing and batch disposition operations. Specific Responsibilities: Support global recipe management strategy to maximize reuse of recipes and/or recipe segments across sites Build recipes that are designed around simplicity, flexibility, and cost effectiveness Partner with MS&T and Process Robustness team to configure recipes in support of analytics Contribute in recipe delivery process including Partnering with Supply Chain, MS&T, Quality, and Manufacturing Operations to understand business requirements Recipe authoring, demos and dry run facilitation Recipe User Acceptance Testing Recipe and master data installations and promotions Ensure recipes are built with consistency and adhere to guidelines Perform recipe and specification review and approvals Gather and manage requirements around batch reports that relate to the Review by Exception and Release by Exception strategies Tier 3 escalation support of recipes and process to minimize disruption to manufacturing and/or impact to product Support strategy for collecting end user feedback and improving the usability and user experience of the overall EMES solution Support risk and impact assessment that changes, patches, outages or other events can have to the EMES solution and the global network and define mitigation strategies. Support a knowledge management strategy including generating training content Promote compliance with data integrity and computer system validation requirements and regulations Promote compliance by understanding change and the impact to the validated state of the application and underlying infrastructure. Qualifications Bachelor s degree in engineering, Computer Science or related fields. 1 to 2 years of experience in software development. Experience in Emerson Syncade/WerumPasX Good Understanding of SDLC (Software Development Life Cycle). Experience using or configuring Manufacturing Execution Systems is a huge plus. Experience in the Life Sciences industry or in a regulated manufacturing environment is a plus. Good understanding of the application of IT to manufacturing, including a broad understanding of processes and how they are supported by IT tools and systems is a plus. Knowledge of regulatory landscape and experience with software validation is a plus. Ability to work across global sites and cultures. Ability to effectively communicate with both technical and non-technical team members. Good written and verbal communication skills. Knowledge of cGMP regulations. Ability to provide on-call support. Ability to interpret / write technical documents Ability to work as a team Quick Leaner If you come across a role that intrigues you but doesn t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms. com . Visit careers. bms. com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers. bms. com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Summary Sr. Analyst, Reimbursement I&A - TAs, play a critical role in supporting the delivery of high-quality, actionable insights for strategic business decisions. The role is responsible for directly contributing to the preparation of key deliverables including, but not limited to, IPST, CPT, IDS POD, BPR and adhoc materials ensuring data accuracy, analytical rigor, and effective integration of Hyderabad s contributions. About the Role Key Responsibilities Responsible for day-to-day delivery of analytics by being 100% hands on for respective tagged project/assignment, not limited to daily ad-Hocs, BPRs, IPSTs, CPTs, IDS POD requirements Deliver and continuously upskill the level of insights for every deliverable ( why questions ) and be responsible for any quality concerns with respective deliverables Responsible for comparing numbers/analysis across similar reports and ensure triangulation of numbers throughout, thus enabling business solutions through a holistic lens Have complete understanding of data , comprising of NPS ARDs and base tables, in order to answer deep dive questions End to end understanding and hands on knowledge of all KPIs, their nuances and exceptions Proactively communicating on personal and professional challenges to leads (on time) to enable quick resolution Maintain documentation of all codes and business rules for enterprise usage (usage of enterprise rules rather than re-inventing new ones) Essential Requirements: Masters/ bachelor s in technology/ life-sciences/ management Experience in patient analytics and US pharma is a must. Strong technical and functional expertise in analytics Experience of 3-5 years in pharma or industry with wide maturity of analytics and reporting Experience in advanced excel, SQL, Python/R, DataIKU Experienced in consulting with good communication skills, along with proven record of the same Ability to ask questions and help design analytical solutions for broad business needs Experience in understanding and designing wide variety of complex data models Expert understanding of enterprise standard platforms, tools and technologies Passion and commitment to drive results through unbossed wow and growth mindset Desired Requirements: Strong communication skills with flexibility to adapt wow for different cultures Strong analytical thinking with problem solving approach Should have exposure to cross-functional/ cultural work environment Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients lives. Ready to create a brighter future together? https://www. novartis. com / about / strategy / people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork. novartis. com/network Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

Clinical Validation Analyst- Office based- Bangalore/ Chennai/ Trivandrum We are currently seeking a Clinical Validation Analyst to join our diverse and dynamic team. As a Clinical Validation Analyst at ICON, you will play a critical role in ensuring the accuracy and integrity of clinical trial data through rigorous validation processes. You will contribute to the success of our clinical programs by analyzing data and implementing validation protocols that support regulatory compliance and data quality. What You Will Be Doing: Conducting data validation and quality assurance checks to ensure the integrity of clinical trial data. Collaborating with cross-functional teams to define validation requirements and develop validation plans. Identifying and resolving data discrepancies, documenting findings, and recommending corrective actions. Supporting the development and maintenance of validation documentation, including protocols and reports. Staying updated on industry best practices and regulatory requirements related to data validation. Your Profile: Degree in life sciences, statistics, computer science, or a related field. Experience in clinical data management, validation, or a related role within a clinical research environment. Strong analytical skills and attention to detail in data analysis and validation processes. Familiarity with statistical software and data management tools. Effective communication skills, with the ability to collaborate with diverse teams and stakeholders. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Clinical Validation Analyst- Office based- Bangalore/ Chennai/ Trivandrum ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Validation Analyst to join our diverse and dynamic team. As a Clinical Validation Analyst at ICON, you will play a critical role in ensuring the accuracy and integrity of clinical trial data through rigorous validation processes. You will contribute to the success of our clinical programs by analyzing data and implementing validation protocols that support regulatory compliance and data quality. What You Will Be Doing: Conducting data validation and quality assurance checks to ensure the integrity of clinical trial data. Collaborating with cross-functional teams to define validation requirements and develop validation plans. Identifying and resolving data discrepancies, documenting findings, and recommending corrective actions. Supporting the development and maintenance of validation documentation, including protocols and reports. Staying updated on industry best practices and regulatory requirements related to data validation. Your Profile: Degree in life sciences, statistics, computer science, or a related field. Experience in clinical data management, validation, or a related role within a clinical research environment. Strong analytical skills and attention to detail in data analysis and validation processes. Familiarity with statistical software and data management tools. Effective communication skills, with the ability to collaborate with diverse teams and stakeholders. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Job_Description: Role: Senior Executive/ Assistant Manager Product Management Team Reporting to: Senior GM Sales & Marketing Department: Sales & Marketing Location : Mumbai Key Responsibilities: 1. Strategic Brand Planning Develop and execute comprehensive brand strategies aligned with corporate objectives. Identify market opportunities and threats through detailed market analysis and competitor benchmarking. Define clear brand positioning and messaging to differentiate the product in the marketplace. 2. Cross-Functional Collaboration Work closely with Research & Development (R&D), Medical Affairs, Regulatory, Sales, and Supply Chain teams to ensure cohesive brand development and execution. Coordinate with global and regional teams to adapt strategies to local market needs and regulatory requirements. 3. Marketing and Promotional Activities Lead the creation and implementation of marketing campaigns, including digital, print, and in-person engagements, ensuring compliance with industry regulations. Manage promotional materials and training programs for sales teams to enhance product knowledge and sales effectiveness. 4. Market Research and Analysis Conduct ongoing market research to gather insights into customer needs, market trends, and competitor activities. Utilize data analytics to assess brand performance and adjust strategies accordingly. 5. Lifecycle and Portfolio Management Oversee the product lifecycle from launch through maturity, implementing strategies for brand extension and innovation. Manage the product portfolio to maximize profitability and market share. A Pharmaceutical Brand Manager (PBM) is a pivotal role within the pharmaceutical industry, responsible for driving the success and growth of a specific drug or healthcare product. This position encompasses a blend of strategic planning, cross-functional collaboration, and market analysis to ensure the brands objectives are met effectively. 6. Compliance and Regulatory Adherence Ensure all marketing and promotional activities adhere to ethical standards and regulatory guidelines. Collaborate with legal and regulatory teams to navigate complex healthcare compliance landscapes. Skills and Qualifications Bachelorus degree in Pharmacy, Life Sciences, Business, or a related field; an MBA is often preferred. 3-5 years of experience in pharmaceutical marketing or brand management. Strong analytical skills with the ability to interpret market data and trends. Excellent communication and interpersonal skills for effective stakeholder engagement. Proficiency in project management and the ability to lead cross-functional teams. In-depth understanding of the pharmaceutical industry, including regulatory requirements and market dynamics.

Reveal HealthTech partners with a range of clients across the health care and life sciences industries to improve their use of data via machine learning and AI to better serve their own customers and patients. Were looking for a creative and detail-oriented Marketing Designer to join our Product Design team and support our Marketing and Sales efforts. You ll work cross-functionally with teams across Marketing, Sales, and Product Design to bring to life a range of collateral from sales decks and case studies to digital campaigns and conference materials. Our brand is continually evolving, and you ll play an active role in shaping both our tactical design systems and broader strategic expression. This role is ideal for a designer who can balance creativity with clarity, and who understands how to communicate complex ideas with precision and visual impact. Responsibilities include: Design clear, compelling marketing and sales assets tailored for a B2B audience in healthcare and life sciences Collaborate closely with marketers, sales professionals, and product designers to translate complex information into visually engaging deliverables Help refine and expand our brand s visual identity as it evolves to meet the needs of specific industry audiences Balance multiple projects and timelines while maintaining a high standard of design quality and consistency Contribute to the development of our visual strategy from day-to-day production to long-term brand initiatives Have 3-5 years of experience in marketing or graphic design, preferably within a B2B or highly regulated industry like healthcare, life sciences, or technology Be proficient in one or more design tools (Figma and Adobe Creative Cloud

Job Overview Individual contributor with advanced knowledge acquired from several years of experience in the professional discipline. Works independently under limited supervision. Essential Functions Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone project, with guidance from senior staff as appropriate; Competently writes regulatory and/or technical documents with minimal review by senior staff; Establishes relationships with many customers; may meet face to face without rest of team to discuss regulatory issues and present lessons learned. Adopts a proactive and flexible approach to resolve any issues; Undertakes detailed review and management of budgets related to projects, including out of scope activities. Ensures revenue is recognised and challenges when appropriate, may seek guidance from senior staff as appropriate; May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development; May present to clients at bid defense meetings by phone or in person, for a range of regulatory deliverables, at discretion of senior staff; May write new regulatory standard operating procedures, and/or propose revisions and/or act as reviewer for regulatory standard operating procedures, as assigned and appropriate. May be involved in a Regulatory and/or IQVIA Initiative; Performs other tasks or assignments, as delegated by Regulatory management; May manage meetings with Regulatory Agencies; May be assigned as Reviewer and/or Approver for Regulatory standard operating porcedures or cross-functional standard operating porcedures owned by other operations; May support global regulatory or technical initiatives or act as a regional representative on a cross-functional initiative; Performs other duties, as business needs require; Qualifications Bachelors Degree Degree in Lifescience or related discipline Req Or Masters Degree Degree in Lifescience or related discipline At least 8 years relevant experience Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate; Possesses a specific regulatory or technical expertise. Sufficient knowledge of managing regulatory projects, project deliverables on a time bound manner; Expert in planning and delivering work on time keeping quality parameter in mind; Knowledge of regulatory procedures in appropriate region - particularly marketing authorization transfers and relevant cross-functional dependencies; Good working knowledge of regional regulatory intelligence; Ability to work closely with client regional heads to determine the MAT, Regulatory Publishing & submission strategy and execute marketing authorization transfer plan, if applicable; Good understanding of pharmacovigilance activities relevant to transfer of marketing authorization; Ability to establish and maintain effective working relationships with coworkers, managers and clients; Strong software and computer skills, including Microsoft Office, publishing applications and tools, as applicable; Ability to work on several projects, with direction from senior staff as appropriate; Ability to follow standard operating porcedures consistently; provides independent thought to assist in process improvements; Ability to make decisions on discrete tasks under senior supervision; Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education; Experience of involvement in regulatory strategy and determination of documentation requirements, timelines, budgets for MATs, Publishing projects; Project leadership experience; Makes adjustments or recommended enhancements in systems and processes to solve problems or improve effectiveness of job area; Problems faced are general and may require understanding of broader set of issues, but typically are not complex; Ability to adapt quickly to a rapidly changing environment; Applicable certifications and licenses as required by country, state, and/or other regulatory bodies . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

About the Role As a Project Support Coordinator, you will get an opportunity to wear a hat of a Project Manager & a Data Analyst. In this hybrid role, you will be coordinating with the CFTs for overseeing and managing projects from initiation to completion, ensuring they meet business goals and deadlines, while also leveraging data to drive decisions and improve processes. Skills & Core Competencies: Organized: Set priorities, develop a work schedule, monitor progress towards goals, and track details / data / information / activities. Communicate Effectively: Speak, listen, and write in a clear, thorough, and timely manner using appropriate and effective communication tools and techniques. Collaborate with CFT (Foster Teamwork): Work cooperatively and effectively with others to set goals, resolve problems, and make decisions that enhance organizational effectiveness. Make Decisions: Assess situations to determine the importance, urgency, and risks, and make clear decisions which are timely and in the best interests of the organization. Risk & Issue Management: Identify potential project risks and develop mitigation strategies. Address any issues that arise during the project lifecycle, ensuring minimal disruption to timelines and deliverables. Project Reporting & Documentation: Provide regular status updates and project reports to senior management and stakeholders. Ensure that all project documentation is organized and up to date. Data Collection & Analysis: Gather, clean, and analyze large datasets to identify trends, patterns, and insights. Transform raw data into actionable reports and dashboards. Candidate Requirements: 2-4 years of work experience Proficient in Microsoft Excel and Power Point University Degree in a related field (i.e., Business, Data, etc.) Strong problem-solving skills and the ability to think analytically and strategically. Excellent communication and interpersonal skills to effectively collaborate with cross-functional teams and stakeholders. Detail-oriented with excellent organizational and time management skills. Ability to prioritize and manage multiple tasks simultaneously while meeting deadlines. . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Job Overview Candidate will be part of South Asia Finance team and will be responsible for various tasks related to invoicing, accounting, collection areas in accordance with IQVIA Finance Standard Operating Procedures (SOPs), US Generally Accepted Accounting Principles (US GAAP), Sarbanes-Oxley rules and financial reporting requirements of the business unit (e.g. local GAAP). Role requirements Analyze, prepare and process accounting entries; analyze, maintain and reconcile general ledger accounts. Prepare profit and loss, income and balance sheet statements. Maintain inter-company accounting records and reconciliations. Provide records of assets, liabilities and other financial transactions. Prepare ad hoc reports for internal and inter-departmental use. Prepare reports and analyze for use in the annual external audit. Ensure accuracy and compliance with all accounting regulations and Sarbanes Oxley requirements. Check that appropriate approvals are obtained for accounting purposes. Provide recommendations to improve existing processes and suggest alternatives where appropriate. Prepare monthly bank account reconciliations. Recommend, develop, implement and / or maintain standards for functional roles. Maintain receipts and disbursement reports. Interpret reports and records for managers. Perform other duties as assigned. Qualification and Skills Chartered Accountant (CA) with 1-2 years of experience in accounting/ within finance function Knowledge of Indian GAAP and US GAAP and excellent accounting skills Understanding and working knowledge of SAP modules Knowledge of Microsoft Office applications. Excellent attention to detail and analytical skills Ability to exercise judgment within procedures and practices to determine appropriate action. Ability to prioritize and coordinate multiple work requirements to meet deadlines Excellent communication skills and Team player IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at Save this job LEARN ABOUT HOW WE WORK Join our Global Talent Network Let s stay connected. Sign up to receive alerts when new opportunities become available that match your career ambitions.

Th ne, India| Bengaluru, India| India| Remote Save this job Job Description Job Overview Receive, digitize, analyze and interpret electrocardiograms (ECGs) received from trial sites according to study specific trial protocol, ECG criteria and Cardiac Safety Services work instructions. Essential Functions Measure, analyze and interpret the ECGs (paper/ digital) received, as per ECG interpretation guidelines and project-specific requirements. Scan and digitize paper ECG s as per SOP s outlined for Paper Study. Perform quality control on ECG reports on assigned days (paper/ digital) before they are faxed to trial sites. Understand and comply with core operating procedures and work instructions of Cardiac Safety Services. Maintain operational responsibility for managing study specific requirements. Perform clinical quality control of the ECGs (paper/digital). Assist in the induction process, mentoring and training of new Cardiology Associates. Qualifications Other Any of the following medical qualifications - M.B.B.S., B.H.M.S., B.A.M.S and at least 1 year relevant experience within the field of Cardiac Monitoring or equivalent combination of education,training, and experience. Computer Literate Ability to work well within a team Ability to establish and maintain effective working relationships with coworkers, managers, and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at Save this job LEARN ABOUT HOW WE WORK Join our Global Talent Network Let s stay connected. Sign up to receive alerts when new opportunities become available that match your career ambitions.

In This Role, Your Responsibilities Will Include: Platform Transformation Support the end-to-end transformation from OCD to a new configuration platform. Help define product vision, goals, and success criteria in alignment with business strategy. Contribute to a phased migration plan that ensures business continuity during the transition. Cross-Functional Collaboration Represent the user perspective and translate stakeholder needs into actionable requirements. Work closely with sales, engineering, ERP, and PLM teams to gather, clarify, and prioritize needs. Product Backlog Contribution Write and maintain clear, detailed user stories, acceptance criteria, and technical notes. Contribute to backlog grooming and prioritization based on user value, technical effort, and business priorities. User Experience Alignment Collaborate with UX/UI teams to shape intuitive, consistent user experiences. Review wireframes and prototypes; provide input to ensure usability and adherence to product requirements. Participate in usability testing and synthesize feedback into actionable enhancements. Technical Collaboration Engage with solution architects and development teams to validate feasibility of configuration logic and model structures. Understand key concepts including rules modeling, BOM generation, product variants, and integrations with ERP/PLM systems. Contribute to discussions around APIs, data flows, and security considerations. Agile Execution Support Actively participate in Agile ceremonies including sprint planning, reviews, and retrospectives. Track key metrics related to product performance, releases, and issue resolution. Ensure that product development aligns with governance standards and compliance policies. Who You Are: You are a seasoned Product Owner who thrives in complex, enterprise environments. While not in a leadership role, you bring thought leadership and a collaborative mindset, contributing significantly to product direction, execution, and cross-functional alignment. Basic Qualifications: 10+ years of experience as a Product Owner or similar role in enterprise software or product configuration environments. Strong experience with product configurators, including hands-on experience with Oracle Configurator Developer (OCD); exposure to modern platforms is a plus. Demonstrated success in Agile product delivery and cross-functional collaboration. Solid understanding of user-centered design practices, usability feedback, and design review processes. Preferred Qualifications: Experience with rule-based configuration logic, variant management, and guided selling. Familiarity with ERP/PLM integration points and enterprise systems. Knowledge of API-driven architectures, middleware, and data integration. Exposure to modern front-end frameworks such as React. js is a plus. Bachelor s degree in Computer Science, Engineering, Business, or related discipline. . Emersons compensation and benefits programs are designed to be competitive within the industry and local labor markets . We also offer a comprehensive medical and insurance coverage to meet the needs of our employees. We are committed to creating a global workplace that supports diversity, equity and embraces inclusion . We welcome foreign nationals to join us through our Work Authorization Sponsorship . We have established our Remote Work Policy for eligible roles to promote Work-Life Balance through a hybrid work set up where our team members can take advantage of working both from home and at the office. Safety is paramount to us, and we are relentless in our pursuit to provide a Safe Working Environment across our global network and facilities. Through our benefits, development opportunities, and an inclusive and safe work environment, we aim to create an organization our people are proud to represent. Our Commitment to Diversity, Equity & Inclusion This philosophy is fundamental to living our company s values and our responsibility to leave the world in a better place. Learn more about our Culture & Values and about Diversity, Equity & Inclusion at Emerson . If you have a disability and are having difficulty accessing or using this website to apply for a position, please contact: . WHY EMERSON . We have built an engaged community of inquisitive, dedicated people who thrive knowing they are welcomed, trusted, celebrated, and empowered to solve the world s most complex problems for our customers, our communities, and the planet. You ll contribute to this vital work while further developing your skills through our award-winning employee development programs. We are a proud corporate citizen in every city where we operate and are committed to our people, our communities, and the world at large. We take this responsibility seriously and strive to make a positive impact through every endeavor. . Emerson is a global leader in automation technology and software. Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability. With global operations and a comprehensive portfolio of software and technology, we are helping companies implement digital transformation to measurably improve their operations, conserve valuable resources and enhance their safety. We offer equitable opportunities, celebrate diversity, and embrace challenges with confidence that, together, we can make an impact across a broad spectrum of countries and industries. Whether you re an established professional looking for a career change, an undergraduate student exploring possibilities, or a recent graduate with an advanced degree, you ll find your chance to make a difference with Emerson. Join our team let s go!

Career Category Safety Job Description The primary responsibility of this role is to perform quality control reviews of of Amgen s Periodic Aggregate Safety Reports (PASR) e. g. Development Safety Update Report (DSUR), Periodic Benefit Risk Evaluation Report (PBRER)/Periodic Safety Update Report (PSUR), Semi Annual Safety Update Report (SSUR), Periodic Adverse Drug Experience Report (PADER/PAER), Device PSUR, and country specific reports e. g. Korea PSUR, Brazil PSUR and Colombia Clinical Research Annual Safety Report Submission and Evaluation form. The QC Reviewer will ensure accuracy, consistency, and compliance with regulatory and company standards. This role supports the end-to-end writing and documentation process and ensures timelines are met. Key Responsibilities: Conduct thorough quality control reviews of PBRER/PSURs, DSURs, PADER/PAERs, and other aggregate safety reports to ensure content accuracy, data integrity, formatting consistency, and adherence to regulatory and internal requirements. Verify correct incorporation of safety data, narratives, tables, and appendices, ensuring alignment with source documents and databases. Collaborate with Periodic Report Specialists to address discrepancies and ensure timely resolution of quality issues. Maintain up-to-date knowledge of global regulatory requirements and industry best practices for periodic safety reporting. Contribute to the development and refinement of QC checklists, templates, and SOPs to ensure consistent review practices. Track QC metrics and support continuous improvement initiatives related to safety report quality and delivery. Basic Qualifications and Experience: Total experience: 5-9 years At least 2-3 years in QC Bachelor s or Master s degree in Life Sciences or Pharmacy .

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Beckman Coulter Life Sciences, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact innovating at the speed of life. At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results. We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory. It s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we re just beginning. Working together, let s put our time and talents together to advance human health for tomorrow. Learn about the Danaher Business System which makes everything possible. The Technician is responsible for labeling, Dispensing & Packaging and responsible to handle unit operation of Packaging instruments. Responsible to meet the FPY and OTD Targets for production as per planning schedule. This position reports to the Abhishek Desai and is part of the Reagents Manufacturing located in IND - Bangalore North - Beckman Coulter India Private Limited and will be an on-site role. In this role, you will have the opportunity to: Understand the process for label printing, Tube Treatment, Packaging and responsible to handle unit operation of Packaging instruments. Responsible to meet the FPY and OTD Targets for production as per planning schedule. Escalation to respective supervisor in case of any downtime or issues in line. Meet regulatory requirements and follow internal company policies, SOPs, good understanding in GDP, cGMP requirements. Must have good communication and be able to support in urgent countermeasures for day-to-day issues occurred at Gemba and keep up to date to all Associates during Daily Management. Candidate should be able to take ownership for his own Packaging KPI and get it tracked by day-to-day to achieve the daily target. Support for On Time delivery to the customer. The essential requirements of the job include: B.Sc or Diploma with minimum 1 2 year experience. Travel, Motor Vehicle Record & Physical/Environment Requirements: Not Applicable It would be a plus if you also possess previous experience in: Not Applicable Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info . At Beckman Coulter Life Sciences we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Life Sciences can provide. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/vision insurance and 401(k) to eligible employees. Note: No amount of pay is wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole discretion unless and until paid and may be modified at the Company s sole discretion, consistent with the law. Join our winning team today. Together, we ll accelerate the real-life impact of tomorrow s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London, Zurich and Gurgaon. Serving clients in the biopharmaceutical, medical device, and diagnostic spaces, we provide world-class strategic decision-making support across a diverse range of business issues. Our goal is to inform actionable recommendations that allow companies to achieve their business objectives. Role Overview We are seeking a dynamic and experienced Senior Recruiter to join our Talent Acquisition team in Gurgaon. In this role, you will lead end-to-end recruitment efforts for early career (campus) and experienced recruiting for our billable teams as well as experienced recruiting for our corporate team. You ll partner closely with hiring managers, and business leaders to attract top talent and ensure a seamless candidate experience. This position reports to our Global Talent Acquisition Manager based in the United States. Manage full cycle recruiting for experienced hires across billable and corporate (from initial engagement through offer negotiations and onboarding handoff). Partner with hiring managers to understand role requirements, define sourcing strategies, and build strong talent pipelines. Collaborate with your Manager and Global Head of Talent Acquisition to ensure alignment on hiring goals and timelines. Conduct candidate sourcing through various channels including job boards, social media, and employee referrals. Screen, interview, and assess candidates to ensure alignment with role requirements and company culture. Drive a high-quality candidate experience throughout the recruitment process. Maintain accurate and up-to-date data in the applicant tracking system (ATS). Develops and maintains comprehensive recruitment dashboards and reports to track key performance indicators (KPIs), analyze hiring trends, and provide actionable insights to TA leadership and senior leadership for strategic workforce planning Provide market insights and data-driven recommendations to improve hiring strategies. Support employer branding initiatives and campus engagement activities for our India office. Support UK recruiting as needed. Qualifications Bachelors degree in Human Resources, Business, or a related field. 4+ years of experience in recruitment, preferably in a fast-paced professional services environment. Strong experience with sourcing tools and applicant tracking systems (e.g., Greenhouse, etc.). Excellent communication, stakeholder management, and organizational skills. Ability to manage multiple requisitions and priorities with a high level of attention to detail. Knowledge of the Indian talent market, especially in Gurgaon/NCR region, is a plus. What We Offer A collaborative and inclusive work environment. Opportunities for career growth and development. Competitive compensation and benefits. Hybrid work flexibility, in office expectation for this role is 50%. We encourage you to apply even if you don t meet every single qualification. We are looking for individuals who are passionate about our mission and are eager to grow and learn. ClearView Healthcare Partners ("CV") is an Equal Opportunity employer. All qualified applicants will be considered for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by applicable law. We encourage you to apply even if you don t meet every single qualification. We are looking for individuals who are passionate about our mission and are eager to grow and learn. ClearView Healthcare Partners ("CV") is an Equal Opportunity employer. All qualified applicants will be considered for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by applicable law.

Position : Business Development Executive (Healthcare Education) Locations : Dehradun (Uttarakhand) Hyderabad (Telangana) Work from Home (for exceptional candidates) We are seeking passionate and result-driven Business Development Executives / Learning Consultants to guide and convert aspiring healthcare professionals into successful learners. You ll be the first point of contact for those looking to study, work, and settle abroad in countries like Australia, the UK, Ireland, and the Gulf through international licensing exam preparation. Your role will involve: Making 100+ outbound calls/day and speaking with 40+ potential learners Conducting 2-3 video counselling sessions daily Understanding candidate goals, recommending the right courses/pathways Converting leads into enrollments through a consultative sales approach Following up with leads and tracking data in CRM tools (LSQ, etc.) Meeting and exceeding weekly/monthly KPIs Shift Timings : 9:00 AM to 6:00 PM (IST) 12:00 PM to 9:00 PM (IST) (Rotational) Salary : Up to 8 LPA (based on experience & performance) 1-3 years of experience in EdTech sales , academic counselling, or inside sales Bachelors or Master s degree (preferably in pharmacy, life sciences, or healthcare) Excellent communication skills in English & Hindi Strong understanding of consultative sales Target-driven mindset with empathy and professionalism Familiarity with CRM tools and Google Workspace Willing to work 6 days/week and handle shift-based work You should be someone who genuinely wants to help others grow not just sell, but guide.

Medical Reviewer-Drug Safety Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation. Job Title : Medical Reviewer Location : Mysore-Hybrid Function : Drug Safety Services ESSENTIAL DUTIES AND RESPONSIBILITIES: Oversee overall Pharmacovigilance (PV) and risk management activities. Review all appropriate data for product specific reports. Provide draft and review (carried out by separate individuals) all single/aggregate/cumulative medical assessments/benefit risk assessments for safety reports. Provide medical oversight white creating draft reports based on the approved SOP/WI process. Coordinate internal review process and finalize draft reports from medical point of view. Assist medical writer in addressing all comments from client and finalize. Should review the finalized report even if participated in assisting medical writer. Provide expert guidance in PV and Aggregate reporting areas. Coordinate all post marketing regulatory reporting and PV activities for assigned products to be carried out by Sitero aggregate reporting team. Preparation of sections of medical significance/inputs for aggregate safety reports such as PSUR, PBRER, Periodic Adverse Drug Experience Report (PADER), Summary Bridging Report, Addendum to Clinical Overview, DSUR, RMP, and addendum to PSUR. Responsible for the medical assessment, recommendation, and conclusion section of the Aggregate Safety Reports. Prepare and review responses to adhoc regulatory queries. Appropriate scientific interpretation of relevant information for inclusion into drug safety documents, prepare and write analytical aggregate reports and other drug safety medical documents. Creating all documents in accordance with applicable Standard Operating Procedure (SOPs), conventions, and regulatory requirements. Planning, organizing, and managing daily work to meet service level timelines and deliverables. EDUCATION AND EXPERIENCE REQUIRED: 1-3 years experience in Clinical Practice required. 1+ yr of experience in Drug Safety and Pharmacovigilance in pharmaceutical or biotech company, CRO or regulatory agency within Drug Safety/Pharmacovigilance, with both investigational and marketed products is preferable. Medical Degree (MBBS or higher) from recognized medical school. COMPENSATION & BENEFITS: Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits. EMPLOYMENT TYPE: Permanent, Full Time COMMITMENTS: Standard Hours 40 hours per week, one hour lunch, Monday - Friday. Additional hours as needed. Willing to work in shifts as and when needed. DISCLAIMER: Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.