2346 Life Sciences Jobs - Page 13

Industry : Hospitals / Medical / Healthcare Equipments Key Skills : Medical LAB Technologist, Mlt, Bsc Mlt, MSC Mlt, Medical Coding Trainee, Medical Coding Freshers, Medical Coder, Pharmacy, Physiotherapy, BPT, MPT, Staff Nurse, Biotechnology, Biomedical Engineer, Biochemistry, Microbiologist, Biotechnologist, Biology, Male Nurse, Walk, Industry : Hospitals / Medical / Healthcare Equipments Function : Health Care / Pharmaceuticals / Medical Positions : 89 Experience : 0 - 1 Yrs. Salary : INR 325000 - 400000 Location(s) of Job : Chennai, Coimbatore, Karur, Nagercoil, Salem, Thoothukudi, Vellore, Theni, Nelson Manickam Road, Chennai, Hosur Taluk, Krishnagiri Qualification : BDSBAMS, B.Pharma, B.Sc, B.Tech, M.Pharma, M.Sc, M.Tech, MVSC Medical Coding is the Fastest-growing Profession in the Healthcare Industry Today. It is a Niche Specialization and the Demand for Trained and Certified Medical Coders is Increasing Exponentially and Bound to Increase in Upcoming Years, Especially in India. you have At Least a Diploma/degree in Any Field. this Role is Open to Fresh Graduates with Excellent English Communication Skills. you Pay Strong Attention to Details and are Capable of Delivering Top-quality Work you are Goal-oriented and Thrive in Fast-paced Environments maintains a Working Knowledge of Cpt-4, Icd-10-cm, and Icd-10-pcs Coding Principles, Governmental Regulations, Uhdds (uniform Hospital Discharge Data Set) Guidelines, Aha Coding Clinic Updates, and Third-party Requirements Regarding Coding and Documentation Guidelines. Hr Bhavani 9566284629

Experience:2 to 4 years of exp. in Scientific or Medical Writing, and/or Quality and regulatory experience in post market surveillance. Exp. with medical device, orthopedic or trauma devices preferred. Required Candidate profile Education B. Tech / B.E in a field related to the life sciences or a relevant medical engineering field (biology,physiology,biomaterials, biomedical engineering or similar). Desired Skills:PMS,EU MDR

EWM Senior Associate, with strong ATTP (pharma) experience. Good communication skills. Strong experience in ATTP skills and integration with EWM Mandatory Skills - SAP ATTP Skills Nice to have skills - SAP EWM

Should have knowledge in Clinical Data Management Should have good knowledge in edit checks crf design SAE Reconcilation crf annotation Clinical Data Management Trained Candidates Only Eligible Required Candidate profile Strong understanding of clinical data management and E2b Guidelines Excellent clinical assessment and Communication Skills

You will be joining Amgen, a company that leverages biology and technology to combat challenging diseases and enhance people's lives by providing innovative medicines to millions of patients. With a history of over 40 years in the biotechnology industry, Amgen continues to pioneer innovation through the use of cutting-edge technology and human data. As a Senior Software Architect at Amgen's AI & Data Innovation Lab, you will play a crucial role in the software engineering practice by developing top-tier talent, establishing engineering best practices, and promoting full-stack development capabilities within the organization. Your primary responsibilities will involve designing end-to-end architecture for digital products incorporating AI features, ensuring performance, robustness, and scalability, as well as selecting frameworks and tools to enable standardization and repeatability. You will collaborate closely with software and AI engineers to choose data models, develop modeling approaches, and define versioning strategies and continuous delivery processes for models and APIs. Additionally, you will be responsible for overseeing model monitoring and maintenance processes, scaling strategies, and establishing pipelines for model deployment and retraining. Your role will also involve conducting architectural reviews, developing standards and best practices in AI and full-stack engineering, and providing technical mentorship to the engineering team. To excel in this role, you should have a deep understanding of software engineering best practices, proficiency in software product development lifecycle, and proven experience in designing end-to-end solutions with modular components and APIs for scale, low latency, and high availability. You should also possess expertise in data flow within AI systems, model monitoring, maintenance, scaling, and deployment strategies, as well as proficiency in backend languages and frameworks, web technologies, and databases. Furthermore, familiarity with enterprise software systems in life sciences or healthcare domains, big data platforms, data pipeline development, and knowledge of data security and privacy regulations would be advantageous. Strong communication skills, problem-solving abilities, attention to detail, self-motivation, and the ability to foster a collaborative work environment are essential for success in this role. Basic qualifications for this position include a Bachelor's degree in Computer Science, AI, Software Engineering, or a related field, along with a minimum of 8 years of experience in full-stack software engineering, including at least 3 years in an architecture role. At Amgen, we are committed to providing equal opportunities for all individuals, including those with disabilities, by offering reasonable accommodation throughout the job application process, interview process, essential job functions, and other employment benefits and privileges. If you require any accommodations, please reach out to us to request assistance.,

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers, and consumers worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning, bold ideas, courage, and passion to drive life-changing impact to ZS. At ZS, we honor the visible and invisible elements of our identities, personal experiences, and belief systems - the ones that comprise us as individuals, shape who we are, and make us unique. We believe your personal interests, identities, and desire to learn are part of your success here. Learn more about our diversity, equity, and inclusion efforts and the networks ZS supports to assist our ZSers in cultivating community spaces, obtaining the resources they need to thrive, and sharing the messages they are passionate about. The ZS Data Office and Strategy team has two pillars. First, The ZS Data Office is dedicated to shepherding ZS Data Strategy. We work collaboratively with Clients and the Client Service Teams, Practice Areas, Expertise Centers, and Enterprise stakeholders to help drive growth and value through the compliant use of data. We build relationships and partnerships with a wide range of data providers to enable ZS access and use of the data in innovative offerings and services. Second, we advise clients on all matters related to Data Strategy. With the explosion of healthcare data and new applications, Data Strategy has emerged as a key strategic initiative for many Life Science companies. The team advises clients on data operating models, data governance, data sourcing and generation, data management, value creation, and data compliance. The Data Office Director, based in Noida (India), will oversee a local team of 10-15 people providing data advisory services to our Client Service Teams and Practice Areas. Using an in-depth understanding of the healthcare data landscape, existing data partnerships, and internal processes, he/she will lead the team in advising ZS stakeholders on the potential data options to support ZS clients and internal projects while ensuring the compliant use of data. He/she will also help deliver world-class solutions that address the development of data strategies to optimize data governance and operation, data sourcing strategy, process design, value creation and portfolio analytics, and more. This individual will have high visibility within the firm and work collaboratively with the rest of the Data Strategy team located in North and South America, Europe, as well as various practice areas. Maintain an in-depth understanding and expertise in the global healthcare data landscape, including key data assets available at ZS and through our partnerships with data vendors. Collaborate closely with ZS practices and client service team leaders to identify data needs, advise on viable data partners, determine engagement models with data partners, and related activities that contribute to the development of new ZS offerings, assets, and solutions that leverage data. Work collaboratively with the team to maintain positive relationships with data partners. Serve as a Subject Matter Expert to support teams in practice area innovation, client project proposals, client discussions, thought leadership, etc., where data expertise is needed. Partner with ZS leaders and client teams to sell and deliver Data Strategy projects for Life Science clients, including project scoping, approach definition, project management and execution, communication, people management. Define and build long-term Data Strategy assets and offerings (new capabilities, frameworks, processes, and tools); and author thought leadership content. Expand awareness, knowledge, and usage of data partnerships within the firm; communicate use cases, facilitate training, create thought leadership documents, etc. Manage and collaborate with an extended team of diverse skill sets (knowledge management, technologists, business operations, etc.). Lead, hire, and develop local team members, setting and meeting high expectations, ensuring constant skill development. Partner with the Senior Leadership team and oversee local project management i.e., Project planning, staffing management, people growth, etc. Mentor/coach junior members in the team. Adhere and supervise team members" adherence to compliance standards in all activities. Bachelor's or master's with a quantitative focus such as Life Science, Physics, Business, Analytics with strong academic performance. 10+ years of relevant job experience; prior experience in Data Strategy and Life Sciences, working with consultancy firms, life science companies, or healthcare data providers preferred. Knowledge of healthcare data and experience of its practical applications (e.g., patient-level EHR, claims, omics, data and experience with RWD/RWE projects or omics data) preferred. Empathy, adaptability, and high personal impact, with the ability to develop and maintain senior relationships; Executive level oral and written communication skills. Demonstrated ability to lead a team with consistently high standards, grow people, and collaborate successfully across geographies. Ability to translate unstructured problems into actionable processes and approaches, and ensure execution by others. Self-starter, with high motivation, maturity and personal initiative. Discipline for planning and organizing tasks for self and the team; managing competing priorities, in a fast-paced context. ZS offers a comprehensive total rewards package including health and well-being, financial planning, annual leave, personal growth, and professional development. Our robust skills development programs, multiple career progression options and internal mobility paths, and collaborative culture empower you to thrive as an individual and global team member. We are committed to giving our employees a flexible and connected way of working. A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections. Travel is a requirement at ZS for client-facing ZSers; business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed. Travel provides opportunities to strengthen client relationships, gain diverse experiences, and enhance professional growth by working in different environments and cultures. At ZS, we're building a diverse and inclusive company where people bring their passions to inspire life-changing impact and deliver better outcomes for all. We are most interested in finding the best candidate for the job and recognize the value that candidates with all backgrounds, including non-traditional ones, bring. If you are interested in joining us, we encourage you to apply even if you don't meet 100% of the requirements listed above. ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law. Candidates must possess or be able to obtain work authorization for their intended country of employment. An online application, including a cover letter, is required to be considered. NO AGENCY CALLS, PLEASE. Find Out More At: www.zs.com,

Are you an experienced project manager with a passion for driving change and delivering results Are you ready to take on a challenging role in a global pharmaceutical company We are looking for a Global Associate Project Lead to join our team at Novo Nordisk. If you have excellent communication and collaboration skills, and a strong background in project management, then read on and apply today for a life-changing career. The Global Associate Project Lead at Novo Nordisk will work closely with the Global Project Lead under the guidance of the Manager Global Insulin Marketing, Diabetes Therapy Areas. In this role, you will be responsible for driving and supporting the overall strategic planning, preparation, and execution of the roll-out plan for Portfolio Consolidation Excellence Framework. Your duties will also include ensuring strong execution of portfolio consolidation decisions, collaborating with stakeholders across the organization to ensure broad alignment and navigate efficiently, as well as spearheading training initiatives and ensuring effective dissemination of knowledge through strategic planning, execution of "Train the Trainer" sessions, and provision of comprehensive training materials with affiliates and operation teams. To be successful in this role, we are looking for someone with a minimum of 8 years of relevant experience in brand communications, training, marketing, strategic planning, or related functions within the life sciences or pharmaceutical industry. You should possess outstanding written and verbal communication skills, with experience in communications development preferred. Proven project management skills, including project planning, stakeholder management, and driving project deliverables within quality and timeline are essential. Strong collaboration and interpersonal skills to work effectively within the team and across the organization, as well as a passion for driving change and continuous improvement, are also key qualifications we seek. The Strategic Diabetes Commercial Communications role is part of the Commercial, Global Business Services (GBS) unit at Novo Nordisk. The Commercial GBS unit is responsible for driving deliverables for multiple Corporate Vice President (CVP) areas within Commercial Strategy & Corporate Affairs, including Insulin, GLP-1 and Obesity Marketing, Market Access, Commercial Planning, and Commercial Operations. In the Diabetes Therapeutic Area, the team is passionate about helping millions of people with diabetes achieve better health outcomes through innovative medicines and solutions. Projects are executed across a strong portfolio comprising both launch and life-cycle management brands. Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on a strong legacy within diabetes, the company is growing massively and expanding its commitment, reaching millions around the world and impacting more than 40 million patient lives daily. The success of Novo Nordisk relies on the joint potential and collaboration of more than 63,000 employees worldwide. To submit your application, please upload your CV online by clicking on Apply and following the instructions. The deadline for applications is 8th September 2024. Novo Nordisk is committed to an inclusive recruitment process and equality of opportunity for all job applicants. The company recognizes the importance of creating an inclusive culture that celebrates the diversity of its employees, the patients served, and the communities operated in. Together, Novo Nordisk is life-changing.,

Job Description: As an Executive Support in our organization, you will be responsible for managing the Medical Director's calendar, meetings, appointments, and travel plans. You will act as the primary point of contact for both internal and external communications on behalf of the Medical Director. Your role will involve drafting, reviewing, and managing official correspondence, reports, and presentations. Additionally, you will coordinate documentation and approvals that require the Medical Director's attention while handling confidential and sensitive information with integrity and discretion. In the capacity of Clinical Coordination & Reporting, you will support the Medical Director in collating, organizing, and presenting clinical data, audits, and departmental reports. Your responsibilities will include assisting in preparing medical dashboards, mortality/morbidity reports, clinical quality indicators, and compliance summaries. You will also be required to liaise with Heads of Clinical Departments, Nursing, Quality, and Operations for both routine and special reviews, as well as maintain and update performance tracking tools related to clinical KPIs and hospital-wide quality metrics. Additionally, you will coordinate and document Clinical Committee meetings such as the Medical Advisory Board, Infection Control, and Quality Review Meetings. In the role of Administrative Liaison, you will act as a bridge between the Medical Director's office and various departments including HR, Quality, Operations, and Accreditation teams. Your duties will involve monitoring the timely implementation of directives issued by the Medical Director to different departments, following up on action items, deadlines, and the progress of strategic and operational tasks. Furthermore, you will support in coordinating hospital-wide initiatives led by the Medical Director, such as NABH compliance, clinical excellence programs, and patient safety drives. Desired Qualifications & Experience: - Graduate in any discipline; preference will be given to candidates with a background in Healthcare Management, Life Sciences, or Nursing. - Minimum 3-5 years of experience as an executive assistant, PA, or coordinator, preferably in a hospital or healthcare setting. - Familiarity with hospital workflows, medical terminology, and accreditation standards (NABH/NABL/JCI) is highly desirable. - Proficiency in MS Office (Excel, Word, PowerPoint) and hospital MIS/reporting tools. Key Competencies: - Excellent verbal and written communication skills - Strong organizational and multitasking abilities - High attention to detail and process orientation - Discretion in handling confidential information - Professional demeanor with interpersonal finesse - Analytical mindset with the ability to interpret basic clinical data This is a full-time position requiring in-person work at our location.,

This is a critical role related to the implementation of process and technology solutions for the diagnosis, analysis, and transformation of the Demand and Supply Planning functions in a project. As a SAP APO DP and SNP Lead, your key responsibilities will include architecting, designing, and assisting in building successful implementations of SAP APO DP and SNP in customer organizations. You will also collaborate with Sales and Delivery Teams to support the growth of Services Business around APO in alignment with Organizational strategy and goals. Moreover, mentoring Junior APO Team members on APO DP and SNP will be a crucial aspect of your role. Additionally, you will drive the development of Assets and Accelerators within SAP APO DP and SNP to reduce the overall cost to serve. To excel in this role, you should have at least 10 years of Supply Chain Planning experience, with a minimum of 8 years specifically in SAP APO DP and SNP modules. You should have led at least 3 end-to-end APO DP and SNP implementations, excluding rollouts. Experience in SAP IBP and SAP certification would be advantageous. Deep process understanding of end-to-end Supply Chain planning, familiarity or expertise with the SCOR model, and proficiency in at least 2 industries such as CPG, Chemical, Automotive, or Life Sciences are essential. Your technical expertise should encompass a good understanding of all modules of SAP APO with a specialization in DP and SNP. You should possess extensive knowledge and experience in end-to-end APO implementation projects in Process and Discrete industries. Your ability to lead Design workshops, architect end-to-end solutions using APO DP and SNP, work on complex configuration scenarios, and write functional specifications for customizations will be critical. Experience in Lifecycle planning, Promotional planning, forecasting using Advanced Statistical algorithms, and expertise in either SNP Optimizer and/or CTM, Deployment, and TLB are desired. Furthermore, you should have excellent communication skills, both verbal and written, along with a positive attitude, flexibility, and maturity to work in challenging client environments. Conducting trainings and mentoring junior APO team members will also be part of your responsibilities. Bristlecone, the leading provider of AI-powered application transformation services for the connected supply chain, is committed to empowering customers with speed, visibility, automation, and resiliency to thrive on change. With transformative solutions in Digital Logistics, Cognitive Manufacturing, Autonomous Planning, Smart Procurement, and Digitalization, Bristlecone offers a comprehensive portfolio of services. As an equal opportunity employer, Bristlecone values diversity and inclusion in its workforce. As a part of the Information Security responsibilities, you are required to understand and adhere to Information Security policies, guidelines, and procedures to protect organizational data and Information Systems. Participation in information security training, reporting of suspected security breaches, and compliance with additional information security responsibilities pertinent to your job role are essential aspects of this position.,

As a Ph.D holder in Life Sciences, you will be responsible for independently carrying out a project within the specified domain. Your expertise and knowledge in Life Sciences will be crucial in contributing to the success of the project. It is expected that you will apply your research skills and experience to drive the project towards its objectives. Your role will involve conducting thorough research, analyzing data, and drawing meaningful conclusions that can further enhance the understanding within the field of Life Sciences. You will be required to demonstrate a high level of proficiency in your area of specialization and be able to work independently with minimal supervision. To be successful in this position, strong communication skills, attention to detail, and the ability to work effectively in a team are essential. Your dedication to advancing knowledge in Life Sciences and your passion for research will be highly valued in this role. If you believe that you possess the necessary qualifications and skills for this opportunity, we encourage you to send your latest resume to careers@xcyton.com. We look forward to reviewing your application and potentially welcoming you to our team.,

You will be joining a dynamic team working on a technology-driven platform within the biotech and life sciences sector. Leveraging AI and digital solutions, we aim to revolutionize scientific workflows. As the Chief Scientific Officer (CSO), you will be responsible for leading our Research and Development (R&D) efforts, defining our product strategy, and fostering industry partnerships. In this pivotal role, which is at a co-founder level, you will have significant ownership and wield strategic influence within the company. Your key responsibilities will include shaping the scientific and technical strategy for our cutting-edge biotech Software as a Service (SaaS) platform. By identifying market needs in biotech, pharma, and analytical sciences, you will guide our platform design, AI integration, and product development. Moreover, you will be tasked with establishing strategic partnerships with academic institutions, biotech firms, and research labs. Ensuring regulatory compliance, such as Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and International Organization for Standardization (ISO), will be part of your mandate. You will also be instrumental in devising monetization models and crafting business growth strategies for the company. The ideal candidate for this role would possess a PhD, MSc, or MTech in Biotechnology, Bioinformatics, Life Sciences, or related disciplines. Previous experience in scientific R&D, biotech startups, Contract Research Organizations (CROs), or pharmaceutical companies will be advantageous. Additionally, familiarity with SaaS, AI-driven tools, or digital solutions in the biotech and life sciences domains is highly desirable. A robust network within academia, biotech, and research organizations, coupled with a keen interest in business strategy and scaling technology-driven ventures, would make you an ideal fit for this position. In return for your contributions, we offer a competitive compensation package that includes Equity (Employee Stock Ownership Plans - ESOPs) or a Co-Founder-Level Stake. This role presents the opportunity to lead scientific innovation within a high-impact biotech startup. You will have the chance to spearhead the development of a scalable, AI-powered solution that caters to the scientific community, shaping the future of scientific research and digital transformation.,

As a Secondary Market Research Senior Consultant at IQVIA, you will be a valuable member of a global technology team consisting of over 82,000 employees, located in Bangalore, Gurugram, and Pune. Your role will involve assisting life sciences companies in accelerating innovation to enhance human health by leveraging transformative technologies that integrate industry-leading data and analytics. Your primary responsibility will be to deliver strategy and management consulting projects, which include conducting Market Assessments, basic forecasting, data Analytics, strategic market reviews, Go-To-Market (GTM) strategies, competitive profiling and analysis, and pharmaceutical industry analysis. Your problem-solving skills will be crucial for conducting integrated desk research, epidemiology studies, quantitative analysis using IQVIA data assets, storyboarding, stakeholder and project management, business development support, people management, and process improvement. Your operational responsibilities will include background and experience with Market Assessments, Basic Forecasting, Data Analytics (Power BI), and a strong quant aptitude with intensive knowledge of the Pharmaceutical and Life Sciences sector. You will assist in commercial due diligences for local pharma clients, support business plan development, and perform extensive analysis and research to build a detailed understanding of target markets, companies, or opportunities based on client problem statements. You will be expected to source information through secondary research and IQVIA data sources, integrate qualitative and quantitative data to present structured analysis and value-added insights to clients. Undertaking market analysis, including market characteristics, competitor characteristics, and prescriber characteristics, will be part of your responsibilities. You will also deliver high-quality, client-ready output with minimal supervision, identify risks/issues, and escalate them to project leads in a timely manner. To qualify for this role, you should hold a Graduate/Post-graduate degree in Life Sciences from a premier institute and have 8 to 11 years of experience in a client-facing role within Pharmaceutical/Biotechnology/Consulting/Professional Services Outsourcing company. Demonstrated hands-on expertise in one or more practice areas, strong analytical, problem-solving, interpersonal, and presentation skills are essential for this position. Additional requirements include the ability to synthesize qualitative and quantitative data, create a collaborative team spirit, structure project research approaches using cross IQVIA resources, and extract key learnings independently. Strong interpersonal, communication, research, analytical, and presentation skills are necessary, along with a high sensitivity to deadlines, attention to detail, adaptability, and resilience to work constructively under pressure. IQVIA, a leading global provider of clinical research services, commercial insights, and healthcare intelligence, aims to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. If you are self-motivated, proactive, and possess the required skills and expertise, we welcome you to join our team. Learn more at https://jobs.iqvia.com.,

1.To perform cleaning of Visual inspection equipment in fill finish facility. 2.To Perform visual inspection of Vials, PFS and Cartridge along with documentation. 3.Making entries in log books, batch packing record and status labeling. Required Candidate profile 1. Looking for smart and dynamic pharma fresher candidate. 2. Candidate should be very good in to written and oral english communication 3. Candidate should be very dynamic.

In billions of syringes and in every second car worldwide, Datwyler components make an important contribution to the safety of patients and drivers The high-tech company focuses on high-quality, system-critical elastomer components and holds leading positions in attractive global markets such as healthcare, mobility, connectivity, general industry and food & beverage With over 25 production sites on four continents, sales in more than 100 countries and over 8,000 employees, the company, headquartered in Switzerland, generates annual sales of more than CHF 1,000 million Our employees are the heart of Datwyler we treat each other with respect, trust and appreciation We have strong roots and values that have been well established in our 100-year corporate history Become part of our great team as a Technical And Scientific Expert (TSE) Datwyler focuses on high-quality, system-critical elastomer components and has leading positions in attractive global markets such as healthcare, mobility, oil & gas and food & beverage With its recognized core competencies and technological leadership, the company delivers added value to customers in the markets it serves With more than 20 operating companies, sales in over 100 countries and some 7,000 employees, the Datwyler Group generates annual sales of more than CHF 1,000 million In this high visibility, high impact role within Datwyler Healthcare, you will consult with global pharmaceutical and biotech companies to co-develop novel, life-saving drug packaging solutions As a member of the Technical and Scientific Services (TSS) Team, the TSE position is based in the US and will report into the Global Head of TSS The TSS team is a global, customer-facing team that works alongside Sales, Marketing, and Product Management to realize the business objectives of Datwyler Healthcare You will deliver excellent scientific support and insights to the external customer and to internal stakeholders As a TSE you will be tasked with the following responsibilities: Implementing the scientific strategy of assigned customer accounts Leading the technical sales process Positioning Datwyler Healthcare products to external customers based on scientific insights and technical information Listening to the customer and the business to collect pertinent scientific and technical information Adapting flexibly to customer situations, profiles, and expectations Acting internally as the voice of the customer for scientific matters Acting as the interface between the external customer and internal technical functions in the pursuit of tactical and strategic goals Addressing scientific inquiries from customers and bringing solutions in a timely manner Being proactive and forward-looking in upcoming scientific trends with a view to initiating internal projects Being aligned with Business Strategy, Product Strategy and Customer Strategy Acting as a scientific knowledge center for Datwyler Healthcare and continually improving internal knowledge and products through market insights Bringing integrity, accuracy, and competence to assigned tasks: ?We sell confidence? Building Datwyler Healthcares scientific and technical credibility internally and externally through: Delivering technical presentations at conferences or webinars, provide customer trainings, and internal trainings Building a scientific knowledge base through industry associations and attending external conferences and trainings Acting as a networker to build scientific relationships at customers in the pharmaceutical and biotech industry Collecting information at events and customer interactions to support product and commercial strategy What are we looking for from you Key Attributes: A curious, learning mind with a can-do attitude Affinity for technical and scientific discussions with pharmaceutical and biotech customers Ability to work in a cross-functional, matrixed environment, within a global team Scientific, technical, or engineering background coupled with business acumen Willingness to learn about Datwyler packaging components, specifically elastomers and their usage in drug packaging Location and Travel: This position is remote with periodic travel to Datwylers Pune site Residing close to pharmaceutical hubs in Western or Northern India is a plus Willingness to travel to conferences, trade shows, customer visits (20-30%) Affinity for attending targeted events to build out network with customers Comfortable with domestic and international travel Qualifications: D Educational background or experience in the Life Sciences, such as drug research or formulation, is a plus Knowledge of drug products and therapeutic classes is a plus Experience: 10+ years Be yourself at Datwyler We are convinced that people make the difference At Datwyler, you will experience diversity and a wide range of career opportunities that only an international company can provide Together, we are increasing our agility, accelerating digitalization and fostering sustainability For motivated and talented employees, we offer interesting development opportunities with training and assignments in a global environment With us, you can contribute with all of your creativity and all your ideas datwyler,

Aragen is looking for Junior Research Associate to join our dynamic team and embark on a rewarding career journey As a Research Associate, you will be responsible for conducting research and analyzing data to support various research projects Conduct research studies and analyze data using a variety of research methods and tools Analyze and interpret data using statistical software and other analytical tools Prepare reports and presentations summarizing research findings and conclusions

Manage the end-to-end execution of AI projects within the supply chain, from planning through to delivery. Collaborate with cross-functional teams, including data scientists, software developers, and supply chain experts, to define project requirements and objectives. Develop detailed project plans, including timelines, budgets, resources, and risk management strategies. Coordinate project activities, ensuring alignment with strategic objectives and adherence to project scopes and deadlines. Serve as the primary point of contact for project stakeholders, facilitating communication and engagement to ensure project success. Monitor project progress and performance, utilizing metrics and analytics to drive improvements and report on outcomes. Identify and resolve project issues and risks promptly, maintaining focus on achieving project goals. Advocate for best practices in AI implementation and project management, fostering a culture of innovation and continuous learning. The essential requirements of the job include: Bachelor s degree in Business Administration, Engineering, or a related field; PMP or relevant certification preferred. Proven experience as a Project Manager in AI or technology-driven supply chain projects. Strong understanding of AI technologies and their applications within supply chain management. Excellent organizational and leadership skills, with the ability to manage multiple projects simultaneously. Effective communication and interpersonal skills, with experience in stakeholder management and team collaboration. Analytical and problem-solving abilities, with a focus on driving efficiency and innovation. Proficiency in project management tools and methodologies, with a track record of successful project delivery. It would be a plus if you also possess previous experience in: Working experience or knowledge about adjacent business domains such as Commercial/Sales/Marketing, Manufacturing operations, Supply Chain management, etc Familiarity with Danahers business model and commercial activities. Danaher 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.

Regulatory Affairs Associate II Job Details | Teva Pharmaceuticals Find a Career With Purpose at Teva Search by Postal Code Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Regulatory Affairs Associate II Navi Mumbai, India, 400706 Who we are The opportunity The RA Associate II is responsible for preparing and revising high-quality US Gx labeling documents submitted under an ANDA and/or 505(b)(2), as required. This role ensures compliance with federal regulations, guidance documents, and internal procedures while meeting deadlines aligned with company objectives. The candidate must demonstrate the ability to work with minimal supervision and possess a thorough understanding of US FDA labeling regulations and guidance documents, applying this knowledge effectively across all work output. Additionally, they will be responsible for creating compliant Structured Product Labeling (SPL) files, ensuring complete drug listing information, and adhering to compliance requirements for importation, bulk listings, and related processes. How you ll spend your day Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and ensure labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents Develop US labeling documents needed for early development projects requiring a human factor or comparative analysis study and ensure established labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents with all relevant departments Some experience in developing labeling content that requires carve-outs due to protected language associated with patents/exclusivities Establish and maintain SPL for assigned projects. Ensure product data elements align with the required drug listing regulations and established SPL is submitted through FDA s Electronic Submission Gateway Prepare and electronically compile full responses to the FDA via the appropriate filing mode. This includes, but is not limited to, the development of side-by-side comparisons, SPL, and other required submission materials, as necessary Perform quality reviews of labeling and submission documents by proofreading established files for content accuracy, either manually or by utilizing the electronic proofreading tool TVT Work closely with external departments, including CMC and the Device team, to align with internal product/device strategy and process Work closely with Regulatory Operations, as well as in Teva s publishing software, to ensure assigned projects are submitted on time following the eCTD requirements related to labeling Support products falling under Business Development deals, if required, from a labeling/artwork and drug listing perspective Attend assigned project meetings to ensure labeling timelines are met Maintain an accurate project tracker of all assigned projects with identified due date priorities and timelines of initial assignment, initiation, and completion of projects Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling Work in a team environment with minimal supervision Perform all other job-related duties as required by management and dictated by process changes Your experience and qualifications Bachelors in pharmacy/masters in science & Life sciences - 4-5 Years in the Pharmaceutical Industry Masters in pharmacy - 3-4 Years in the Pharmaceutical Industry Proven experience in regulatory affairs within the pharmaceutical, biotechnology, or medical device industry Be able to multi-task in a fast-paced work environment Have exemplary oral and written communication skills Be organized with keen attention to detail Have the ability to work independently as well as in a team environment with minimal supervision Have knowledge of US FDA regulations and guidance related to US Gx labeling Have knowledge of US FDA regulations and guidance related to US drug listing Have knowledge of US FDA eCTD submission standards and experience in applying these requirements to routine labeling submissions to the FDA PC, Microsoft Office Suite with a proficiency in Microsoft Word and Microsoft Excel Adobe Acrobat Professional is a must Familiarity with TVT preferred Teva s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

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. This Data Science - Intern is responsible for implementing data-driven solutions to support our remote connectivity software platform. This position is part of the Biotech Software Team located in the India Development Center and will be an on-site role. In this role, you will have the opportunity to: Collaborate closely with cross-functional teams, including software engineers, to integrate data engineering solutions into our remote connectivity platform, providing enhanced insights into instrument performance. Design and implement data pipelines to ingest, process, and load data from diverse sources into our data systems. Conduct proof-of-concept studies and feasibility analyses to identify and implement solutions that ensure reliable and accurate data delivery. Leverage available data to develop models and strategies for predictive maintenance of instruments, aiming to reduce downtime and improve reliability. The essential requirements of the job include: Currently pursuing a postgraduate degree in Data Science, AI or related fields. Strong understanding of machine learning algorithms, statistics, and data preprocessing. Proficient in data science technologies and tools, and database management systems. Strong programming skills in languages such as Python. Exposure to cloud-based data platforms such as Azure. 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 . 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 .

RD Data Project manager plays a key execution and delivery role across multiple Sanofi RD imperatives. This role must have a strong understanding of RD business processes and have strong stakeholder management skills. This role must also be familiar with data practices, e.g., data strategy, data management, and data governance, and can communicate effectively to key stakeholders on behalf of the RD Data Office. Main responsibilities: Oversee and coordinate timelines across RD Data Office initiatives within the RDDO and with related/dependent initiatives across the enterprise Oversee maintenance of program plans, communications, templates, etc. Manage demand and provide advice on financial management for priority RD Data Office initiatives, support integration with Finance, Procurement, and other corporate functions Monitor RD Data Office initiative objectives, particularly as they develop RD Data Office Capabilities (e.g., Data Governance, Data Management, etc.) and raise gaps in operating model (e.g., people, process, technology, etc.) Support coordination of preparatory work and briefing materials for key meetings Support and create strategic documents articulating the value of RD Data Office activities Support and create training modules and communications to help with RD data culture and literacy Support the RD Data Office agenda in line with company strategic priorities through monitoring of progress and related KPIs and work with key stakeholders to support delivery Deliverables: Communicate standards for data ownership and hold the data governance council(s) and data owners accountable at a functional level Formulate data governance operations plan (including data strategies, standards, definitions, rules, policies and processes), and procurement, ongoing operation, and maintenance of supporting technology Review and prioritize projects (initiatives) to manage asset inventory, ensure proposed solutions meet business needs, and monitor progress/outcomes Maintain detailed documentation of the change process, including milestones, challenges, and lessons learned About you Experience in Program/Project Management, Business Development, Communications, Change, Data/Tech or related field Experience with Agile Program Management processes Knowledge of drug discovery and development information and processes Change agent with combination of business, technology, and diplomatic skills Strong familiarity with data analytics, data capabilities, and cross-industry data standards Ability to plan and forecast across programs and initiatives Ability to navigate, escalate, and manage risks Demonstrated skillset in transformation / implementation of large-scale programs Understanding of back-end and front-end technologies and experience implementing highly functional solutions that can scale Must have played a role in ensuring organizational adoption of changes that needed significant influencing of business team. Should be adept at defining KPIs for leadership consumption of metrics measuring the adoption and sustainability of such changes Storyteller with the ability to translate complex technical jargon and concepts into something simple, accurate, and easy to understand Expert communication skills: experience with change management and training modules is a plus Excellent communication skills and familiarity with use of social media in enterprise Experience with change management and training modules Education : Bachelor s or master s degree in Life Sciences disciplines (Biology, Chemistry, Bioinformatics, Cheminformatics, etc.)

The overall purpose and main responsibilities are listed below: Support HEVA team in assigned therapy area portfolio to plan and generate robust health economics and value based evidence to maximize the value propositions from both a global and US perspective working within the Market Access tripod Support the execution of quality research projects, economic models, trial design recommendations and other activities in support of programs/products Seek opportunities to innovate HEVA value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA evidence to ensure reimbursement decisions optimal access Develop and maintain TA expertise People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEVA teams across various time zones Performance: (1) Support in the HEVA evidence generation plan: Develop research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs; Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes; Provide strategic support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (2) Support execution of approved HEVA study(s) and manage ongoing study(s) if required: Supports the manager/HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products; Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes (3) Support development of core value dossier (CVD) and AMCP dossiers and provide strategic direction Process: (1) Assist HEVA team in development of HEVA strategic evidence material (2) Assist manager in development of core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (3) Maintain adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes Stakeholder: (1) Work with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables (2) Support HEVA team to prepare relevant customized deliverables for these Teams About you Experience : 5 + years of experience in HEOR for the pharmaceuticals industry, CRO consultancy or academia. Soft and technical skills : Stakeholder management; writing/communication skills; external engagement and ability to work independently and within a team environment Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies; Understands reimbursement decisions to determine value drivers and how evidence is used in decision making and how it impacts various payers (e.g., providers, patients, health systems); Knowledge of methods and principles of health economics, health technology assessment (HTA) reviews 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. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Join an international biopharma company.

Job Description Work on sales force effectiveness projects like Field force sizing, Targeting, Alignment, Call planning, Incentive Compensation, Dashboard reporting for pharma clients Provide Incentive Compensation analytics support to clients and sales force Incentive Operations (Plan Design, Goal Setting, IC administration, and IC reporting). Develop SQL queries based on business rules and develop Tableau dashboards based on defined KPIs Facilitating data enabled decision making for clients by providing and communicating insights recommendations based on qualitative and quantitative analytics. Understand business requirements, operating business rules, data, and underlying processes to communicate results to clients. Understand Pharma commercial data sets like Patient claims data, Rx, SP, SD, Call activity, internal CRM data etc. and can triangulate data from multiple sources that drives commercial effectiveness. Collaborate with onshore team/client for day-to-day project activities and guide team, delegate tasks, and take accountability of end-to-end engagement management. Maintain process assets (SOPs, Checklists, BRDs, Process Maps etc.) and establish best practices. Coach and mentor junior team members for higher responsibilities Qualifications Education: MBA / B Pharma / M Pharma - Life Sciences academic background or B Tech / BE / M Tech / ME - Engineering academic background. Experience and/or Training: 1+ years of relevant work experienc

Atria University, established in 2018, is India s inaugural liberal STEM university. It offers innovative, project-based, and research-focused interdisciplinary degree programs in science, technology, business, and design. Atria University stands out for its strong emphasis on cutting- edge research and its vibrant Centers of Excellence, which serve as high-performance hubs fostering innovation in various fields, including Life Sciences, AI, Energy Sciences, and Battery Engineering. Join Atria to contribute to transformative research and become a thought leader in Life Sciences. Principal Investigator: Dr. Balamurali G.S, Associate Professor. https:// schol ar .google .com/cit Age limit: JRF / Project Assistant: 35 years Duration For one year, extendable to 2 years based on performance. The position is purely temporary and co-terminus with the project. Money JRF = 37,000 + HRA (As per funding agency guidelines) Qualification Minimum of 60% marks (or equivalent grade) in the qualifying degree preferably. Additional qualifications for JRF are: Valid NET or GATE qualification. In case a suitable candidate with the above qualifications is not found, candidates with a Post-graduate degree in Biological Sciences may be appointed as Project Assistant if selected. Emoluments will be as per funding agency guidelines. Experience Experience in Behavioural Ecology and a working knowledge of R is highly desirable.

" Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. The Position Organization- Jubilant Pharmova Limited Designation - Manager- Compliance(Legal) Location- Noida Job Summary: Role is responsible for ensuring that the organization adheres to legal standards, regulatory requirements, and internal policies. This role involves developing and overseeing control systems, conducting audits, managing risks, and fostering a culture of compliance across all departments. Key Responsibilities. Draft, revise, and implement internal policies and procedures. Develop and manage an effective legal compliance program through the formation of a compliance committee. Monitor and interpret changes in laws and regulations. Ensure updates in compliance ownership are reflected in the Conformity tool. Ensure timely completion of compliance status updates by process owners/approvers in the Conformity tool Conduct inspections and validation visits to plant sites/office to ensure on-ground compliance Create action plans in response to findings and ensure implementation of corrective actions. Educate and train employees on compliance standards and regulations. Maintain accurate records of compliance activities. Prepare compliance reports for senior management and regulatory authorities. Conduct monthly meetings with key stakeholders to update compliance status. Person Profile . Qualification - LLB/Master in Finance, or a related field Experience 8+-Years (preferably in similar environment in compliance, legal, or regulatory roles. Jubilant is an equal opportunity employer. . ",

JOB DESCRIPTION Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Cytiva, 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. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Field Applications Specialist is responsible for supporting the Customer, Account Manager, Workflow Specialist, and core commercial team. Provides deep scientific knowledge in the customer context, including tests and demos to prove competitive advantage. This position reports to the Senior Manager of the Gen Med FAS Team in APAC and is part of the Gen Med Commercial APAC Team located in India and will be working remotely to cover India as well as APAC. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Collaborates with Account Managers, and Sales Specialists within their territory based on customer demand for scientific application. Responsible for providing pre and post-sale support, product demonstrations, seminars, training and supporting territory sales objectives. Applies highest level of scientific and technical product knowledge in modality, including solution impact, capabilities and functions within context of Cytiva customers. Supports customers with in-depth technical support, remotely, in person or in the lab. Conducting demos or experiments for or with the customer. Following up on samples with technical advice and/or experimental support. Responsible for regional customer training, developing application driven training courses and demonstrations, at customer sites and high-level scientific meetings. Build and strengthen strong technical relationships with customer. Identify potential opportunities of scalability of an application, identify products and services that will provide significant cost savings and productivity gains for the customer, and persuasively educates and articulates the benefits to the customer. Who you are: Cross selling, upselling, value positions and funnel management. Understanding of customers key business drivers. Insight with networks and contacts. Comprehensive Cell Therapy, Viral Vector or nucleic acid process (upstream/downstream) expertise. Bachelor s Degree in biotechnology, life sciences or relevant field. Preferably in cell biology, biochemistry, and immunology 5 years of applications experience must be from Biotechnology industry. Travel: Ability to travel 50-75 % travel, overnight, within territory or locations It would be a plus if you also possess previous experience in: QlikSense or Sales Force

Provide comprehensive data management expertise to eCOA Data Management to provide efficient, quality data management products that meet customer needs. Provide support in operational eCOA Data Management activities to the eCOA Data Team Lead (DTL) or operate in a specific eCOA DM task (e.g., lead of a task on a megatrial, data reconciliation and monitoring). Essential Functions Serve as Data Operations Coordinator (DOC) for several global clinical trials or serve in a leadership role to a specific data management task. With minimal guidance, serve as back-up for Data Operations Coordinator or Data Team Lead Provide specific eCOA or Clinical DM task or technology expertise. Manage delivery of projects through full data management process life-cycle. With minimal guidance, manage project timelines and quality issues, determine resource needs, and identify and justify out-of-scope. Provide comprehensive data management expertise (including all operations tasks ). Perform comprehensive quality control procedures. Independently bring project solutions to the eCOA DM team. communicate ideas for process improvement. Assist in developing and implementing new technology. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with eCOA DM and project teams. Interact with eCOA DM team members to negotiate timelines and responsibilities." Qualifications Working knowledge of SAS software a plus, but not required. Bachelors Degree Clinical, biological or mathematical sciences, or related field, or nursing qualification Req 3 years of related experience including clinical trials experience in a function similar to data management. Equivalent combination of education, training and experience. Thorough knowledge of the data management process. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Previous experience and proven competence in managing delivery of project through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III). Comprehensive understanding of clinical drug development process. Excellent organizational, communication, and data management skills (detail oriented). Ability to establish and maintain effective working relationships with coworkers, managers and clients. Thorough knowledge of the data management process. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Previous experience and proven competence in managing delivery of project through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III). Comprehensive understanding of clinical drug development process. Excellent organizational, communication, and data management skills (detail oriented). Ability to establish and maintain effective working relationships with coworkers, managers and clients.