169 Scientific Writing Jobs - Page 2

Position Description: The Commercial Learning Services (CLS) Medical Writer is responsible for the development of medical content including but not limited to creating/ updating wireframes, building reference packages, creating/ updating learning content for product trainings for assigned areas at both Global and affiliate level. The CLS Medical Writer will anticipate and adjust for problems and roadblocks, interface with Lilly partners at Indianapolis and Lilly Bengaluru and integrate new business processes where necessary. Using strong adult learning principles, CLS Medical Writer ensures quality design, development, and delivery of training development projects. This role will interact with a wide variety of people both in Lilly Bengaluru and the US, at varying levels of the business The role will report to CLS Group or Team Leader at Lilly Bengaluru. Key Objectives/Deliverables: Medical Writing (Content Development) Partners with learning consultants and business partners to effectively gather and evaluate source content from multiple sources. Plans (including organizing/preparing outlines), write (including first-draft authoring), edit, review, and coordinate the creation of medical learning content (storyboard) Ensures that key content, scientific concepts, elements from internal guidance and resource documents are included appropriately in all learning content, and that all documents are well written, usable/executable, and compliant with policies and procedures. Ensures proper documentation of needed references and attribution of source material. Ensures and coordinates quality checks for accuracy, collate reviewer s comments, adjust content of training as required based on internal/external input, and prepare final version. Drives quality standards through review of project documents, design, deliverables, final learning content and evaluation data. Project and Stakeholder management Lead the writing process and apply effective project management skills to ensure timely completion of high-quality regulatory documents. Effectively manage multiple projects and exhibit flexibility in moving across therapeutic areas, and products, depending on project assignment. Builds, communicates, and manages credible project timelines. Influences or negotiates changes of timelines and content with other team members. Anticipates and mitigates risks to delivery. Anticipates and resolves project/program issues, escalating as appropriate. Knowledge Sharing and Development Maintains and enhances therapeutic area knowledge including disease state and compound(s) for assigned project(s). Maintains and enhances the medial writing skills to align with the audience needs and with the changes in technology and platforms. Provides coaching to others by sharing technical information, giving guidance, answering questions. Networks with others (including other functions and regions) to identify and share best practices. Contributes to process improvements, suggesting opportunities where appropriate. Basic Requirements: Demonstrated experience in technical scientific writing. Demonstrated excellence with program/project management and time management skills. Successful completion of a writing exercise. Demonstrated ability to establish strong business relationships. Ability to work independently and in a team environment. Demonstrated ability in conflict resolution, judgment and managing complexity. Ability to prioritize work and balance multiple projects simultaneously. Strong work ethic, personal motivation, and team player who is dynamic and result oriented Good presentation skills, interpersonal and communication skills, fluent (verbal and written) in English. Ability to operate effectively in an international matrix environment, with ability to work across time zones. Additional Preferences: Experience writing regulatory, clinical trial documents, publications and/or writing deliverables for Medical Affairs communications (slide decks, patient, or HCP materials, etc.). Experience working in a regulated environment. Experience working with US organizations. Strong organizational skills. Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates). Education Requirements: Bachelor s degree in a scientific, health, communications, technology health related field Other Information: Travel may be required. . .

Department New Generation Insulin (NGI) The Position As a Regional Medical Advisor, you will contribute actively to medico-marketing activities in the business area/portfolio and support in implementation of the Medical Affairs strategy in the country. You will be responsible for: Executing the Indian medical strategy into local activities in your designated region Building, maintaining, and nurturing the excellent scientific relationship with all the key influencers and stakeholders Training and educational activities for Physicians and other Health Care Professionals (HCPs) working with diabetes and obesity Medical support to brand team You will also be responsible for: To assist the marketing and sales team in sharpening and positioning product and promotional strategies. Foresee the challenges as well as changing market dynamics and make timely corrective and preventive actions. You will stay updated on scientific knowledge by actively participating in scientific meetings, gathering clinical insights/needs/feedback from key opinion leaders, and communicating with internal stakeholders. Responsible for educating and training the field and marketing personnel and other relevant stakeholders regarding all aspects of disease, product, and therapy relevant to promotional strategy. You will build a strong advocacy of Novo Nordisks portfolio with key external stakeholders through ongoing/robust scientific interactions. Qualifications MBBS/ MD in Pharmacology from a reputed institution. You shall have strong scientific knowledge and interest in diabetes and obesity including both the therapy area and the products, good collaboration with internal and external stakeholders as well as good communication and negotiation. Strong analytical capabilities, with demonstrated experience in analyzing complex situations. Skills for planning, execution, and follow-up are required, with a creative and innovative attitude that will enable you to drive initiatives with operational excellence and strive towards working with both operational as well as more judicious tasks.

Role & responsibilities As a Project Executive (Content Writer) at Cognus Technology, you will play a key role in crafting high-quality, well-researched academic content specifically in the Finance and Medical domains. Youll be responsible for understanding client requirements, conducting in-depth research, and delivering original, insightful content aligned with academic standards. This role is ideal for candidates with a passion for research, strong analytical thinking, and the ability to simplify complex concepts into clear, structured academic documents. Key Responsibilities: Research & Content Creation: Conduct comprehensive research on topics related to Finance and Medical domains. Create clear, structured, and academically sound content tailored to client briefs. Project Management: Handle multiple writing projects efficiently while adhering to deadlines and maintaining content quality. Quality Control: Review, revise, and proofread content to ensure it meets academic standards, includes proper citations, and is plagiarism-free. Client Communication: Interact with clients to gather project requirements, clarify expectations, and provide regular updates. Guideline Adherence: Ensure all work aligns with internal quality benchmarks and academic writing norms. Team Collaboration: Work closely with editors and fellow writers to enhance content quality and meet client satisfaction. Preferred candidate profile Strong domain knowledge in Finance or Medical/Pharma . Excellent research and analytical abilities. Impeccable written English with a focus on academic tone and structure. Time management skills to handle multiple projects. Keen eye for detail and accuracy in writing. Benefits: Dynamic, collaborative work environment Continuous professional development Flexible working hours Supportive team culture Gaming Zone for breaks and recreation In-house Cafeteria

As a member of our global team in the Data Sciences organization, you will play a crucial role in establishing scientific excellence in the development of digital biomarkers and endpoints. Your primary responsibility will be leading the identification, development, and deployment of novel digital endpoints and outcome measures across clinical trials and life cycle management programs. This will involve close collaboration with the Global Digital Health organization to design and validate algorithms extracting clinically relevant insights from various digital health data sources. Your expertise will ensure scientific rigor, clinical validity, and regulatory readiness in this process. In this role, you will be required to embed digital health technologies within evidence generation strategies, advocating for their acceptance in clinical trials and practice. Additionally, you will contribute to key regulatory filings and publications, promoting the adoption of digital endpoints within the global R&D community. Keeping abreast of emerging trends, you will integrate innovative solutions to enhance patient care and clinical research. Your leadership will be pivotal in driving transformation efforts that maximize the potential of Digital Health Technologies. To excel in this position, you should hold a PhD in a quantitative natural science or medical initiative with a focus on large-scale data analysis. A minimum of 7 years of relevant experience in the pharmaceutical or related industry is essential, along with a proven track record in designing and validating digital endpoints or biomarkers for clinical applications. Experience working with data from digital health technologies, familiarity with algorithm development, and deployment in clinical or real-world settings are also required. Furthermore, you should have expertise in digital biomarker/endpoint development, including psychometric and statistical validation, as well as a solid understanding of algorithm development, signal processing, and AI/ML methods as applied to digital health data. Strong stakeholder management skills, the ability to navigate matrixed organizations effectively, and excellent communication and scientific writing skills are crucial for success in this role. Join us in our mission to create access and opportunities for all to develop and grow at their own pace. Be a part of our inclusive and diverse team that is dedicated to sparking discovery and elevating humanity. Apply now and contribute to championing human progress with us!,

As a Clinical Evaluation Medical Writer at Medtronic, you will play a crucial role in developing and updating clinical evaluation documents to support CE Mark submissions and ensure compliance throughout the product lifecycle. Your work will involve close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk according to MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745. You will also be responsible for summarizing and disseminating clinical literature and other available data to share relevant evidence, while managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and responding to technical and clinical questions from internal teams and external healthcare professionals under the guidance of Clinical and Medical Affairs. Success in this role will require strong skills in scientific writing, literature review, data analysis, and clear communication, as well as a proactive and collaborative mindset. Your responsibilities may include independently creating and maintaining clinical evaluation documents in compliance with relevant regulations and company procedures, supporting Medical Information activities by responding to inquiries, conducting literature searches and reviews, reviewing scientific materials for accuracy and compliance, developing reports, identifying and reporting complaints or adverse events, and collaborating with key stakeholders to drive evidence-based scientific decisions. To excel in this position, you are required to have a mastery of a specialty area and full knowledge of industry practices, typically obtained through advanced education combined with experience. A Baccalaureate degree and a total of 8 years of experience with a minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience are also required. Medtronic offers a competitive salary and flexible benefits package as part of its commitment to employees. The company values the contributions of its employees and offers various benefits, resources, and competitive compensation plans designed to support you at every career and life stage. The position is also eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). Medtronic is a global leader in healthcare technology that aims to address the most challenging health problems facing humanity by seeking out innovative solutions. With a mission to alleviate pain, restore health, and extend life, Medtronic unites a global team of passionate individuals who are committed to making a difference. The company values diversity and is dedicated to engineering extraordinary solutions for real people by leveraging talent, diverse perspectives, and ambitious ideas. To learn more about Medtronic's business, mission, and commitment to diversity, please visit their website.,

Role Purpose The purpose of the role is to provide effective technical support to the process and actively resolve client issues directly or through timely escalation to meet process SLAs. Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLAs defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements Deliver excellent customer service through effective diagnosis and troubleshooting of client queries Provide product support and resolution to clients by performing a question diagnosis while guiding users through step-by-step solutions Assist clients with navigating around product menus and facilitate better understanding of product features Troubleshoot all client queries in a user-friendly, courteous and professional manner Maintain logs and records of all customer queries as per the standard procedures and guidelines Accurately process and record all incoming call and email using the designated tracking software Offer alternative solutions to clients (where appropriate) with the objective of retaining customers and clients business Organize ideas and effectively communicate oral messages appropriate to listeners and situations Follow up and make scheduled call backs to customers to record feedback and ensure compliance to contract /SLAs Build capability to ensure operational excellence and maintain superior customer service levels of the existing account/client Undertake product trainings to stay current with product features, changes and updates Enroll in product specific and any other trainings per client requirements/recommendations Partner with team leaders to brainstorm and identify training themes and learning issues to better serve the client Update job knowledge by participating in self learning opportunities and maintaining personal networks Mandatory Skills: Med& Scientific Writing, Regulatory Ser. Experience: 3-5 Years.

Role Purpose The purpose of the role is to provide effective technical support to the process and actively resolve client issues directly or through timely escalation to meet process SLAs. Do Support process by managing transactions as per required quality standards Fielding all incoming help requests from clients via telephone and/or emails in a courteous manner Document all pertinent end user identification information, including name, department, contact information and nature of problem or issue Update own availability in the RAVE system to ensure productivity of the process Record, track, and document all queries received, problem-solving steps taken and total successful and unsuccessful resolutions Follow standard processes and procedures to resolve all client queries Resolve client queries as per the SLAs defined in the contract Access and maintain internal knowledge bases, resources and frequently asked questions to aid in and provide effective problem resolution to clients Identify and learn appropriate product details to facilitate better client interaction and troubleshooting Document and analyze call logs to spot most occurring trends to prevent future problems Maintain and update self-help documents for customers to speed up resolution time Identify red flags and escalate serious client issues to Team leader in cases of untimely resolution Ensure all product information and disclosures are given to clients before and after the call/email requests Avoids legal challenges by complying with service agreements Deliver excellent customer service through effective diagnosis and troubleshooting of client queries Provide product support and resolution to clients by performing a question diagnosis while guiding users through step-by-step solutions Assist clients with navigating around product menus and facilitate better understanding of product features Troubleshoot all client queries in a user-friendly, courteous and professional manner Maintain logs and records of all customer queries as per the standard procedures and guidelines Accurately process and record all incoming call and email using the designated tracking software Offer alternative solutions to clients (where appropriate) with the objective of retaining customers and clients business Organize ideas and effectively communicate oral messages appropriate to listeners and situations Follow up and make scheduled call backs to customers to record feedback and ensure compliance to contract /SLAs Build capability to ensure operational excellence and maintain superior customer service levels of the existing account/client Undertake product trainings to stay current with product features, changes and updates Enroll in product specific and any other trainings per client requirements/recommendations Partner with team leaders to brainstorm and identify training themes and learning issues to better serve the client Update job knowledge by participating in self learning opportunities and maintaining personal networks Mandatory Skills: Med& Scientific Writing, Regulatory Ser. Experience: 1-3 Years.

Job responsibilities include some of the following: Product & Process Knowledge Management: Data gathering ( Product Quality Review, Change Requests, Methods of Production, Genealogical tree and quality reporting, PHF Parking lot (document with the pending point of the previous version of PHF. Manage PHF governance & operational follow up meetings: (kick off, consolidation, follow up ) Write/update the PHF s with information gathered and manage the approval process with identified stakeholders. PHF Publishing in Veeva, Manage AAR with stakeholders, PHF continuous improvement Collaboration and Communication: Work collaboratively with various departments, including MSAT discipline experts, QA, GCC associates. Documentation and right first time: Ensure the consistent quality of the PHF s. Innovation: Identify opportunities for innovation based on scientific advancements and emerging trends ( IA, digitalization, Training and Development: train staff and stakeholders on best knowledge management practices in close collaboration with MSAT information and knowledge management experts. Checking that the PHF knowledge management strategy laid out by the Global MSAT Compliance and Knowledge Management Process Excellence lead is being respected. Basic Qualifications: Bachelor s Degree ideally with a Ph.D. in a relevant scientific discipline (e.g., biology, chemistry, pharmacy ) Experience: at least 10-16 years of experience in pharmaceutical or biopharmaceutical MSAT or a related field. A working experience of at least 3+ years as a scientific writer or in a similar role is key asset. S takeholder engagement experience in an international and matrixial environment. Advanced scientific writing skills and capabilities . Strong communication, team management skills and interpersonal skills. Strong attention to detail and ability to produce high-quality, accurate documents. Uphold the highest standards of scientific integrity and ethics. Analytical and problem-solving skills. Strong knowledge and understanding of Pharmaceutical or Biopharmaceutical environment. Knowledge and understanding of Good Manufacturing Practice (GMP). Knowledge of regulatory requirements and industry standards. Advanced Written and oral fluency in English. Office tools: Classical (word, excel, PowerPoint) and specific (Office Timeline Pro, pdf creator), Documentum & SAP GSK Access (PHF, PQR, general R&D doc, Techshare, ) Veeva GSK Access . Preferred Qualifications: MSAT, or Manufacturing Science and Technology, is a critical function within a pharmaceutical and biopharmaceutical manufacturing organization in general. The GSK MSAT team is responsible for ensuring that products are produced safely, efficiently, and to the highest quality standards. Why GSK? Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Agile and distributed decision-making using evidence and applying judgement to balance pace, rigour and risk Managing individual and team performance. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Implementing change initiatives and leading change. Sustaining energy and well-being, building resilience in teams. Continuously looking for opportunities to learn, build skills and share learning both internally and externally. Developing people and building a talent pipeline. Translating strategy into action - a compelling narrative, motivating others, setting objectives and delegation. Building strong relationships and collaboration, managing trusted stakeholder relationships internally and externally. Budgeting and forecasting, commercial and financial acumen. Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose to unite science, technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. Important notice to Employment businesses/ Agencies

Summary The Medical Expert in TCO (Translational Clinical Oncology) is the medical leader for assigned global, roll-over and long-term follow-up studies, and studies in the close-out phase. They may also provide medical co-leadership for assigned aspects of one or more global, active, TCO study, under the leadership of a Clinical Program Leader (CPL) TCO (Translational Clinical Oncology) is a department under Biomedical Research division, and is responsible for designing and executing out early phase (first in human) clinical studies in patients with cancer. It acts as a bridge between drug discovery and late phase clinical development and strives to deliver transformative new medicines for oncology conditions. About the Role Major accountabilities: Provides medical support to Clinical Program Leader (CPL) leading the program. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables. May act as the medical monitor to support overall program safety reporting (e.g., Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team. May represents CPL at project team meetings (e.g. CTT) and may provide inputs to project strategy May represent CPL at Investigator teleconferences including dose escalation meetings and site initiation visits. Oversees the clinical/scientific elements of TCO related submission documents, including preparation and review of project documentation for Health Authority submission, including briefing books, IBs, Annual Safety Reports, responses to Health Authority questions etc. Leads the ongoing clinical trial data medical/scientific review across assigned TCO studies and coordinates data analysis and interpretation Accountable for assigned close-out, roll-over and long-term follow-up studies, ensuring Clinical Study Report review, consistency and quality of clinical study reports (CSR) in collaboration with CSR medical writing team, and publication of studies across assigned TCO projects - either directly as lead author or by providing leadership to the medical writing team Manages stakeholder engagements internally and externally Mentors and coaches junior TCO team members in India Maintains expert knowledge of ICH-GCP, external regulations and procedures, and supplements by training and practice of Novartis SOPs and internal policies. Leads or assists with relevant trainings across TCO India Advocate continuous improvement of quality Ensure all activities of associates comply with company standards and local regulations Key performance indicators: Management of assigned studies to ensure execution according to timelines, and with high quality, ensuring adherence to international and local regulations. Demonstrates excellent scientific writing skills to enable the development of quality trial reporting, and regulatory documents. Strong evidence of quality medical review of trial data and quality contributions to clinical sections of e.g. protocols, IBs, DSURs and CSRs Contribution towards objectives set for the department. Feedback from external and internal stakeholders. Clearly demonstrates Novartis Values and Behaviors. Minimum Requirements: Education: MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine / pharmacology etc.) with medical council certification required. Experience in hematology / oncology preferred Work Experience: At least 5 years of pharmaceutical/biotech industry experience At least 2 years of clinical practice experience in the hospital setting. Experience with oncology clinical trials Experience with early development clinical trials Knowledge of Good Clinical Practice (GCP). Strong operational project experience including excellent planning, prioritization, problem solving and organizational skills. Used to managing multiple priorities. Demonstrated operational excellence and scientific contribution to both clinical and preclinical projects. Strategic thinking: ability to network with and influence key stakeholders, clear and logical presentation of complex strategic issues. Clear written and verbal expression of ideas, an active/proactive communicator. Well-developed interpersonal skills, with a proven record of accomplishment of successfully interacting with, influencing and building strong positive relationships. Used to working independently and in a team, being flexible and adapting in a changing environment. Skills: Clinical Monitoring. Clinical Research. Clinical Trial Protocol. Clinical Trials. Decision Making Skills. Drug Development. Health Sciences. Lifesciences. Medical Strategy. Regulatory Compliance. Languages : English. Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

JOB DESCRIPTION: JOB CODE: BIOPLUS/MEDCOMM/WH/020 DATE OF CREATION: 7th Feb 2025 Department Marketing/ Medico-marketing Communications Position Scientific Writer / Sr. Scientific Writer Reports to General Manager Marketing Communications Qualification Ph. D/ M. Pharm / B. Pharm / MBBS / BDS / MDS / BAMS / BHMS/ PG in life sciences. Experience Total 4 Years experience in Medico-Marketing in the Pharmaceutical Industry. 3+ years experience in developing scientific and medico-marketing content development for pharmaceutical companies Strong written and verbal communication/presentation skills Ability to translate complex medical concepts into easy-to-understand marketing messages. Ability to collaborate effectively across departments (e.g., Sales, Medical Affairs, Regulatory). Knowledge of the healthcare industry, medical products, and healthcare trends. Location Whitefield Road, Bangalore Type of Work Full time, work from office Company Description: With over 75 years of experience, Bioplus Life Sciences is a pharmaceutical company based in Bengaluru. We focus on advanced Biotechnology and have programs in late-stage clinical phases for global unmet needs. Our pipeline includes pre-clinical programs and blockbuster Novel therapeutics, with a strong emphasis on R&D and Clinical Development. We are delighted to invite you to explore an opportunity of learning, contributing and discovering science and medicine with us as part of our global research team. Bioplus Life Sciences and its subsidiaries Theialife Inc, USA & Akeso Biopharma, Singapore have a novel portfolio of first in class and best in class novel therapeutics in discovery stage to Phase 3 clinical stage. Theialife is currently building a global leadership team in Boston, as a prerequisite to list on NASDAQ. Our lead molecule ND 10 for early onset paediatric myopia control will be applying for EU Marketing Authorization in Q1-2025 and US FDA pre submission meeting NDA meeting also in Q1-2025. As you are probably familiar with the drug discovery journey you will appreciate that is the culmination of 18 years of effort, perseverance, and devotion to a single-minded goal of creating a global biopharmaceutical company. The myopia drug opportunity is itself over USD 20 billion and there is no other therapeutic in clinical development except Atropine which has had efficacy endpoint issues. We are adding new large manufacturing capability including a 2-million-liter microbial fermentation bio foundry and significant dosage form capacity. By 2030 we intend to be amongst the Worlds top 5 Ophthalmology innovation led global companies. To support, build and develop our pipeline we are looking to add Scientists, Doctors and Engineers and Technical People to our team of likeminded dedicated science warriors who have devoted their lives to pursue excellence and contribute to finding medical solutions for significant global unmet medical needs. Job Summary: A Medico Marketing Specialist plays a crucial role in developing and executing Pharma marketing strategies aimed at healthcare professionals, medical organizations, and consumers. This position requires a blend of marketing expertise and a strong understanding of the healthcare industry to promote medical products, services, or solutions effectively. The Medico Marketing Specialist is responsible for creating marketing materials, managing campaigns, and building relationships with healthcare stakeholders, ensuring that marketing efforts align with industry regulations and standards. Key Responsibilities: Responsible to define, develop and execute medico marketing strategies and tactics for various product segments in collaboration with cross-functional stake holders. Analyze market trends, customer needs, and competitors to position products effectively. Define product attributes, go-to-market strategy, product positioning, key benefits, and target customers in association with the Marketing & Sales team. Collaborate with product development teams to align marketing strategies with new medical offerings. Plan, execute, and optimize multi-channel marketing campaigns, including digital, print, events, and healthcare conferences. Manage content creation for promotional materials such as brochures, presentations, website content, and product brochures. Ensure all marketing materials comply with regulatory standards Conduct educational webinars and product demos to engage medical professionals and increase awareness. Respond to inquiries from healthcare professionals and stakeholders in a timely manner. Provide medico marketing tools to field force to enable them for effective communication on promotions. Generate and provide medical content for official websites/ portals. New Product development and launch strategy and support. Regular training and flow of latest medical developments in the given field. Scientific Support and Technical Training to internal and external customers. Identify new opportunities for growth and suggest innovative marketing approaches. Soft Skills: Strong communication and interpersonal abilities to effectively engage with cross-functional teams and stakeholders. High level of analytical thinking, problem-solving, and strategic planning Excellent in people management skill What We Offer: A collaborative, innovative, and supportive work environment. Career advancement opportunities in a leading company at the forefront of biotechnological advancements. Why Join Bioplus? Bioplus offers a unique opportunity to make a significant impact on global healthcare by shaping the commercial success of novel, life-changing therapies. As part of our team, youll collaborate with passionate professionals committed to improving patient outcomes worldwide. Equal Employment Opportunity (EEO) Policy: Career opportunities at Bioplus are provided without discrimination on the basis of race, sex/gender, religion/caste/creed, social or ethnic origin, colour, age, differently abled (including physical medical conditions), sexual orientation, domestic partnership status, gender identity or expression, marital status, ancestry, genetic information or any other reason prohibited by laws in India.

Key Responsibilities: Lead team and oversee content delivery Develop scientific content Manage timelines and strategy Train team and ensure compliance Health insurance Maternity benefits in mediclaim policy Performance bonus Referral bonus Provident fund Paternity leaves Career break/sabbatical Prevention of sexual harrassment policy

A Day in the Life The Clinical Evaluation Medical Writer on our Endoscopy team plays a key role in developing and updating clinical evaluation documents (e.g., CEP, CER, PMCFP, PMCFR, SSCP) to support CE Mark submissions and maintain compliance throughout the product lifecycle. This work follows MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745 and involves close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk. In addition, the writer supports related activities such as summarizing and disseminating clinical literature and other available data to share relevant evidence, while also managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and responding to technical and clinical questions from both internal teams and external healthcare professionals, all under the appropriate guidance of Clinical and Medical Affairs. Success in this role requires strong skills in scientific writing, literature review, data analysis, and clear communication, along with a proactive and collaborative mindset. Responsibilities may include the following and other duties may be assigned. Independently creates and maintains clinical evaluation documents (CEP, CER, PMCFP, PMCFR, SSCP) in compliance with MEDDEV 2.7/1 Rev 4, MDD, EU MDR 2017/745, MDCG guidance, and company procedures. Supports Medical Information activities by leveraging scientific expertise to research and respond to inquiries from healthcare professionals and internal teams, maintaining related documents and reports. Performs thorough literature searches and reviews clinical evidence from studies, reports, and available post-market data. Summarizes and combines this information to support product submissions, clinical evaluations, and Medical Information inquiries. Reviews scientific materials like abstracts, posters, manuscripts, slides, and promotional content to check for accuracy, proper claims, off-label use, and compliance with company policies. Develops state-of-the-art reports for product families and reviews cross-functional documents such as IFUs and Risk Management files to ensure alignment on safety and risk information. Identifies and reports complaints or adverse events from literature to the Global Complaint Handling team. Creates responses to audit and submission queries and maintains a database of peer-reviewed literature. Collaborates with key stakeholders to drive evidence-based scientific decisions and maintain compliance with regulatory and corporate guidelines. Communicates project timelines, input requirements, and risks clearly and promptly with cross-functional teams. Required Knowledge and Experience: Requires mastery of a specialty area and full knowledge of industry practices, typically obtained through advanced education combined with experience. May have broad knowledge of project management. Requires a Baccalaureate degree and total 8 years of experience with minimum 4 years of relevant experience, or advanced degree with a minimum of 2 years of relevant experience. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

About the job: Key responsibilities: 1. Conduct research and experiments to develop innovative biotechnology solutions 2. Utilize scientific writing skills to prepare reports, presentations, and publications 3. Proficiency in MS-Word and MS-Excel to analyze data and document findings 4. Collaborate with cross-functional teams to ensure project milestones are met 5. Demonstrate effective communication skills to present findings to stakeholders 6. Apply knowledge of biology to drive product development and testing 7. Stay current on industry trends and advancements to contribute to continuous improvement efforts Who can apply: Only those candidates can apply who: Salary: ₹ 2,00,000 - 4,00,000 /year Experience: 0 year(s) Deadline: 2025-08-15 23:59:59 Other perks: Free snacks & beverages Skills required: MS-Word, Biology, MS-Excel, Scientific Writing and Effective Communication Other Requirements: 1. Passion for R&D and Laboratory experiments 2. Interest in biotechnology and in vitro diagnostics About Company: Promoters of Levram Lifesciences have a solid track record in the production of polymer goods. A youthful technical team at Levram is working to provide high-quality medical products at competitive prices to serve the Indian market and other markets. We have recently ventured into the dermatology and trichology space and are looking to expand our team out there. This is in ninja mode and our product (and line of products) has gotten a good response from doctors and we are looking to expand this in a big way soon.

The Content Solutions team at Indegene focuses on diverse projects throughout the product life cycle, covering regulatory, safety, medical affairs, and commercial solutions for clients. Leveraging clinical and scientific knowledge, the team addresses various business challenges to engage target audiences such as physicians and patients in different therapy areas. As a member of the team, you will have the opportunity to collaborate with healthcare clients on a variety of projects. Indegene is currently seeking a Scientific Writer and Reviewer to fulfill the role of a quality medical reviewer/technical reviewer for promotional, disease education, and training materials on behalf of a pharmaceutical client. Your responsibilities will include conducting procedural reviews to ensure compliance with MCA guidelines, verifying data accuracy, evaluating content based on references, and correctly interpreting information from sources. The role requires delivering and reviewing high-quality, comprehensive, and timely content. Key responsibilities also involve cross-checking scientific information with references for accuracy, ensuring alignment with approved product labeling, assessing adherence to MCA guidelines, validating reference quality and accuracy, maintaining consistency in reference citation style, verifying the presence of crucial information, defending content based on scientific evidence, and demonstrating a willingness to learn and write for various therapy areas and markets. In addition, you will liaise with client medical and other stakeholders to provide content clarifications, prioritize review assets as per requests, and adhere to agreed-upon timelines for review and submission. To qualify for this position, you should hold an advanced bioscience or pharmacy/medical qualification, possess excellent verbal and written communication skills, demonstrate a strong scientific acumen, and have 1-5 years of experience in the pharmaceutical industry. This experience should include content writing and review related to medical affairs/medical information, literature reviews, publications support, and promotional/non-promotional medical review. The job location for this position is in Bengaluru, Hyderabad, Pune, Mumbai & Delhi NCR on a hybrid work model.,

RRD GO Creative is seeking experienced Medical Writers to join our team in Chennai. In this role, you will play a crucial part in developing high-quality and scientifically accurate medical and regulatory documents, such as clinical study reports, protocols, and brochures. Your responsibilities will also include creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. To excel in this role, you must conduct thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams is essential to develop compelling and compliant medical writing materials. You will be expected to adhere to client and regulatory guidelines, such as ICH, FDA, and EMA, while ensuring consistency, accuracy, and scientific integrity in all documents. As a Medical Writer, you will review and revise content based on feedback from reviewers and editors, manage multiple writing projects simultaneously while meeting strict deadlines and quality standards, and support quality control and peer-review processes to ensure excellence in medical documentation. Requirements for this role include a Bachelor's, Master's, or Doctorate degree in Life Sciences, Medicine, Pharmacy, or a related field, along with at least 3 years of experience in medical writing within the pharmaceutical, healthcare, or life sciences industries. A strong understanding of medical and scientific terminology, clinical research processes, and regulatory requirements is crucial. Additionally, excellent writing, editing, and verbal communication skills are necessary, with an eye for detail. Experience in preparing clinical and regulatory documents, publications, and scientific communications is preferred. You should be able to interpret and summarize complex scientific data for different audiences and possess familiarity with industry guidelines such as ICH, GCP, AMA, FDA, and EMA. Proficiency in Microsoft Office Suite and reference management tools is required, along with strong organizational skills, multitasking abilities, and the capacity to work independently under tight deadlines. Moreover, experience collaborating with cross-functional teams, including researchers, medical professionals, and regulatory experts, will be beneficial in this role. Join RRD GO CreativeTM, a company with over three decades of experience in business communications, marketing solutions, and digital productivity solutions. Our expertise in Global Brand Solutions, Smart Work Solutions, and Technology & Innovation Services enables us to transform the way businesses interact with customers, fostering strong brand loyalty. Our team of 8,000 experts across 42 locations collaborates across various industries to co-create a future-ready business landscape. We work with businesses to digitize every aspect of the Customer Journey, translating strategic visions of expansion and efficiency into superior Customer Experiences. Let us help you address customer needs effectively and make Customer Experience your competitive differentiator.,

The Lv Prasad Eye Institute is renowned for its cutting-edge research and contributions to the field of ophthalmology. Focused on providing world-class eye care solutions, the institute aims to innovate and advance eye care through extensive research and development programs. It is a prominent center for learning and collaboration among eye care professionals. This full-time, on-site role located in Hyderabad is for a Research Optometrist. The responsibilities include conducting clinical research, collecting and analyzing data, and collaborating with other researchers and clinicians. Daily tasks encompass performing eye exams, conducting electrophysiology tests, contributing towards clinical trials, and participating in publications and reports. The role also involves maintaining accurate records and ensuring compliance with regulatory standards. The initial contract duration is 1 year, with the possibility of renewal based on performance. Qualifications for this role include strong clinical skills in optometry, experience in performing electrophysiology tests and data analysis, excellent written and verbal communication skills, ability to work independently and collaboratively, proficiency in scientific writing and contributing to research publications, attention to detail, strong organizational skills, knowledge of regulatory standards and compliance in clinical research, and a minimum of a Bachelor's degree in Optometry or a related field; advanced degrees or certifications are a plus. The salary for this position will be in accordance with the Institute's protocol. Interested candidates can share their CV at amithavikram@lvpei.org.,

As a member of our global team, you will play a crucial role in fostering scientific excellence in the field of digital biomarkers and endpoints within the Advanced Data Science team of the Data Sciences organization. Your primary responsibilities will include leading the identification, development, and implementation of innovative digital endpoints and outcome measures across various clinical trials and life cycle management programs. By collaborating closely with the Global Digital Health organization, you will be instrumental in designing and validating algorithms that extract clinically relevant insights from a diverse range of digital health data sources, such as wearables, sensors, and apps. Your expertise will ensure scientific rigor, clinical validity, and regulatory compliance in all aspects of digital health technology integration. As a subject matter expert, you will be instrumental in incorporating digital health technologies into evidence generation strategies, thereby promoting their adoption in clinical trials and medical practice. Your contributions to key regulatory filings and publications will advocate for the widespread acceptance of digital endpoints within the global R&D community. By staying abreast of emerging trends, you will continually introduce innovative solutions to enhance patient care and clinical research. Your leadership will drive transformational efforts aimed at unlocking the full potential of Digital Health Technologies. Qualified candidates will possess a PhD in a quantitative natural science or medical discipline with a focus on large-scale data analysis, along with a minimum of 7 years of relevant experience in the pharmaceutical or related industry. A proven track record in designing and validating digital endpoints or biomarkers for clinical applications is essential, as is hands-on experience with data derived from digital health technologies like wearables and mobile platforms. Proficiency in algorithm development and deployment in clinical or real-world settings, coupled with a solid understanding of digital biomarker/endpoint development, psychometric and statistical validation, and regulatory considerations is required. Candidates should also demonstrate strong expertise in algorithm development, signal processing, and AI/ML methods as applied to digital health data. Excellent stakeholder management skills, the ability to navigate complex organizational structures effectively, and outstanding communication and scientific writing abilities are also essential qualities for this role. This role is based in Bangalore & Hyderabad, and offers a unique opportunity to work in a diverse, inclusive, and flexible environment that fosters personal development and career advancement on a global scale. Join us in our mission to create a culture of inclusion and belonging that empowers individuals to make a meaningful impact and contribute to human progress through innovation and discovery. Apply now to be a part of a team dedicated to Sparking Discovery and Elevating Humanity!,

A Research Scientist designs, conducts, and analyzes experiments and research projects to advance scientific knowledge and potentially develop new products or technologies. They are responsible for all stages of research, from planning and execution to data analysis and reporting, and often collaborate with other scientists and professionals. Key Responsibilities: Planning and Design: Developing research proposals, designing experiments, and creating research plans. Execution: Conducting experiments, collecting data, and monitoring research progress. Analysis and Interpretation: Analyzing data, interpreting results, and drawing conclusions. Reporting: Writing research papers, reports, and presentations to disseminate findings. Collaboration: Working with other scientists, engineers, and professionals to share knowledge and expertise. Staying Updated: Keeping abreast of new scientific developments, technologies, and research trends. Supervision: May be involved in mentoring and supervising junior researchers or technicians. Funding: Applying for grants and funding to support research projects. Problem-Solving: Identifying and solving scientific problems through research and experimentation. Safety and Compliance: Ensuring research is conducted safely and in accordance with ethical and regulatory standards.

The Medical-Regulatory Writer Assistant Manager will be responsible for planning and managing Medico-Regulatory Writing for Regulatory compliance in accordance with applicable Regulatory Guidelines. You will be tasked with providing high-quality medical and scientific writing services, from planning and coordinating literature searches to delivering final drafts to both internal and external clients. Your role will also involve offering technical consultation, substantive advice on strategy, regulations, and industry best practices, and demonstrating expertise in subject matter and therapeutic areas. In addition, you will need to effectively manage medical writing projects to ensure the delivery of quality products within agreed timelines. Collaboration with internal and external clients will be essential, along with tasks such as writing CTD Modules, Medical Data Packages, SmPCs, PIs, PILs, Safety Reports, Aggregate Reports, and other relevant documents. You will also be responsible for conducting science reviews of aggregate reports produced by PV Associates and ensuring that all document outputs and processes align with client specifications, templates, and style guidelines. Furthermore, the role requires attending project initiation meetings, maintaining awareness of current regulatory guidance and medical information techniques, updating Aggregate Report Tracker, carrying out cases reconciliation periodically, and conducting detailed searches on regulatory agency websites for safety alerts. Mentoring Associates, overseeing training plans, and enhancing the skills of existing team members will also be part of your responsibilities. The ideal candidate should hold a Master's degree in Pharmacology/Pharmacy/Medicine with at least 5 years of experience, although an advanced degree is preferred. Previous experience in the pharmaceutical/CRO industry is advantageous, along with additional qualifications in medical writing such as AMWA, EMWA, or RAC. Strong data interpretation, medical writing, and project management skills are essential, as well as excellent interpersonal, negotiation, oral and written communication skills. Proficiency in Microsoft Word, PowerPoint, and Excel, as well as the ability to work effectively in a team-oriented environment, are also required. This position may occasionally require working in different time zones as needed. There are no direct reports for this role, and the location will be in Gurgaon.,

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 youll 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. ZS's R&D Excellence Practice brings together experts in Strategy, Clinical Execution, Data Sciences and Technology to empower client organizations to achieve their passion for patient care, science and business success. Through our Lifecycle Evidence Strategy, Clinical Trial Optimization, Medical Affairs and Evidence Generation services, we deliver impact where it matters, from early drug development to commercialization. This role will be aligned with ZSs R&D Excellence Practice Area, and particularly within our Evidence Generation practice, supporting our business consulting and analytics services across multiple clients. HEOR/Evidence Synthesis Lead: We seek applicants for Evidence Synthesis Lead role . This is an important leadership role within our Health Economics and Outcomes Research (HEOR) team, part of our Evidence Generation practice. Our vision is to elevate HEOR into a strategic function which bridges the scientific, clinical and commercial spheres, and be the world leading strategic HEOR consultancy. As well as providing core HEOR services, we aim to shape the policy landscape HEOR operates within, be benevolent disruptors, driving the adoption of innovative new approaches, and make HEOR part of the entire product lifecycle. ZS has an inclusive, client centric, consultancy culture, based around our core values: - Treat people right - Get it right - Do the right thing The successful candidate will be someone excited by and aligned to this vision and culture. Responsibilities: Leading evidence synthesis standalone projects and workstreams on broader engagements, as the person responsible for overall quality, timelines, and financial performance Developing recommendations based on expected impact, communicating risks and opportunities to ensure staff alignment, and where appropriate assuming the role of final decision maker Reviewing and signing off on deliverables including protocols, analysis plans, technical reports, and slides Work closely with ZS client teams to lead client business development and client relationship development across our key client accounts; Owning relationships with clients and being viewed as subject matter expert; proactively managing client expectations and working with team members to implement strategies to problem solve on a client or project-basis Leading team development and mentoring, encouraging a culture of open and constructive feedback, ensuring staff have clear pathway for career development Contributing to staffing discussions as well as long-term strategic planning in conjunction with other senior leaders Helping to develop and maintain processes required for the effective operation of the research team (e.g., onboarding, training, templates etc.) Supporting staff to effectively communicate within and across teams, resolving conflicts tactfully, and stimulating morale Providing methodological/subject matter input to and signing off on proposals and presentation content Establishing trusted partnerships with clients and driving new business opportunities Identifying opportunities for growth and recommendations for hiring that aligns with business development Play an active role in counseling and mentoring junior team members within ZS; Demonstrate ability to quickly assimilate new knowledge. May require travel domestically and/or internationally including overnight stays Qualifications: Bachelor's degree in a relevant discipline MSc in relevant discipline preferred, e.g. health economics, public policy, health policy, epidemiology, biostatistics, or public health, or science (biology/biochemistry etc.) Minimum 10 years of directly relevant experience in a similar industry / consulting environment Demonstrates expert understanding of the pharmaceutical industry and requirements for health technology assessment, evidenced by a track record of relevant publications Demonstrated experience with Health Economics and Outcomes Research (HEOR) with a particular emphasis on health Evidence Synthesis e.g. SLRs, ITCs, Dossier Writing etc. Good understanding of relevant methodologies and statistics Ability to lead and manage teams Ability to work seamlessly and collaboratively with teammates across our global practice Excellent communication and interpersonal skills Expertise in communicating HEOR findings in various forms (e.g., peer-reviewed publication, abstracts and conference presentations, HTA dossiers, PowerPoint presentations)

Job Description Research and analyze scientific literature to stay current on developments in relevant fields. Write and edit scientific content for various purposes including articles, blogs, website, emailers, video storyboards and marketing plus printing materials. Collaborate with researchers, subject matter experts, and other team members to ensure accuracy and clarity of scientific content. Translate complex scientific concepts into clear and accessible language for diverse audiences. Ensure that all written materials adhere to established scientific standards, guidelines, and best practices. Manage multiple projects simultaneously and meet deadlines consistently. Assist with the preparation of presentations, posters, and other materials for scientific conferences and meetings. Contribute to the development of scientific communication strategies and initiatives. Stay informed about trends and advancements in scientific writing, API drugs, pharmaceutical, and communication. Ensuring content is user friendly and key-worded for SEO benefit. Participate in team meetings, brainstorming sessions, and other collaborative activities. Job Type: Full-time Schedule: Day shift Experience: total work: 2 years (Preferred) Work Location: In person,

The Executive - PMT will play a critical role in product management and marketing within the nutraceutical or Ayurvedic industry. The role requires strong expertise in scientific research, formulation, regulatory compliance, business development, and training. Department: Product Management Team (PMT) Experience: Minimum 2+ years Industry: Nutraceutical / Ayurvedic Educational Qualification: Master's or Bachelor's in Nutrition, Food Science, Dietetics, or M.Pharm or BAMS Location: Sector 65, Noida Work Timings: 9:00 AM 5:30 PM (Alternate Saturdays off) Key Responsibilities: 1. Business Development Developing formulation propositions and spec sheets. Handling NPDI (New Product Development & Introduction) processes. Preparing product presentations, scientific research, comparison tables, and marketing data. Assisting the BD team with various queries related to formulations and regulatory aspects. 2. New Product Development (NPD) Conducting technical research and feasibility studies for new product development. Coordinating with R&D and other teams for data collection and correspondence. 3. Regulatory Compliance Reviewing artwork, validating scientific claims, and ensuring compliance with regulatory guidelines. 4. Training & Development Conducting monthly training sessions for the BD and regulatory teams. Preparing training materials including PPTs, quizzes, and other learning resources . 5. Event Management Planning and managing events, sponsorships, and exhibitions . Booking stalls, overseeing fabrication, and providing branding materials. Managing bills, payments, and vendor coordination. 6. Social Media & Marketing Collaterals Providing content for brochures, flyers, and leaflets . Proofreading and ensuring accuracy in marketing or promotional materials. 7. R&D Coordination Conducting feasibility checks and gathering product information. Collaborating with the R&D team for product development insights. 8. Business Development (Domestic & Exports) Attending client meetings and supporting the BD team with technical expertise. Assisting in market analysis, competitive research, and strategy development . Key Skills & Competencies: Strong knowledge of Nutraceuticals, Ayurveda, and Functional Foods . Expertise in scientific research, product development, and regulatory compliance . Ability to create engaging presentations and conduct training . Experience in event planning and marketing support . Excellent communication and cross-functional collaboration skills . Interested candidates can apply by sending their CV to hr3@zeon.co.in with the subject line Application for Executive - PMT.

Maintain and update global and local master/reference data across IT systems, ensuring accuracy and alignment with stakeholders. Support project teams, governance boards, and end-users by providing training, guidance, and best practices in data management and key applications. Monitor and improve system performance, data quality, and interface linkages to enhance efficiency and integrity. Lead and implement data quality strategies, including assessments, cleansing, KPI tracking, and continuous improvement initiatives. Act as a subject matter expert and mentor, fostering a collaborative, agile, and learning-focused environment aligned with Novartis' values. Languages : Fluent in English and Telugu (oral and written). Experience/Professional requirement : 1. Knowledge in quality principles driving drug development, such as GMP; understanding of general regulatory and quality expectations. 2. Good scientific background, communication skills including presentation and scientific/technical writing. 3. Minimum 5-7 years in a relevant position in a GMP environment. 4. Sound technical and regulatory knowledge. Working knowledge of pharmaceutical research and technical development. 5. Experienced in GMP environment, with familiarity with IT systems (e.g., eLN, GLIMS, SAP), and interfaces between different data tools.

Project entitled Equitable, Quality universal health coverage Implementation research Project for optimizing comprehensive primary health care through Health and Wellness Centers in Pimpri Chinchwad Municipal Corporation, Pune district of Maharashtra- EQUIP-HWCs funded by Indian Council of Medical Research. Name of the Post :- Consultant (Non-Medical) No. of vacancy :- 01 Consolidated Salary :- Rs.70,000/- Essential Qualification :- Professional having proven competency and success in public health should possess Post Graduate degree in Anthropology / Social Work / Demography / Population Studies / Sociology. Retired Government employees with requisite qualification and who were in the grade pay of Rs.5400/- and above with adequate working experience in the required domain / field. Desirable :- Adequate research experience in Anthropology / Social and Community level Health Research and working with Public Health Department. Age Limit :- Till 70 years Duration :- One Year Place :- ICMR-NIRRCH, J.M. Street, Parel, Mumbai 400012, Maharashtra. Interested candidate can share their cv on this mail id anchal.g@esolglobal.com

Overview Please Note: This is a 6-month contractual engagement which can convert to a full-time job based on performance and business needs. Cactus Life Sciences is a remote-first organization, and we embrace an accelerate from anywhere culture. If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, this role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Responsibilities Taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific and medical materials like manuscripts, abstracts, posters, congress and meetings materials, and literature searches and reviews according to client and audience needs with excellent attention to detail. Actively involved in reviewing materials developed by scientific writers to ensure strategic alignment and scientific accuracy as needed and providing clear constructive feedback, support, and supervision to writers. Having excellent knowledge of product/accounts to enable meaningful interactions with clients and authors, including consultancy where necessary. Liaising and building and maintaining strong and long-standing professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs. This includes educating and advising clients on how to best implement their strategic and tactical plans and proactively provide recommendations to clients on how to improve scientific content and propose new document types/ways to disseminate client date more effectively. Effectively and proactively communicate with team members, authors/faculty, clients and vendors. Attend workshops/seminars/training to hone your skills and contribute to organizational objectives. Attending client and other external meetings and supporting senior team members as needed. Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. Also, supporting with the development of visual content and materials using effective data visualization techniques and approaches. Contributing to innovative out of the box solutions for medical writing projects. You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date. Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines. Supporting with pitches, both during the preparation phase and the actual pitch. Qualifications and Prerequisites Minimum 5 years of experience in relevant fields of scientific writing. PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD OR MPharm/M.Sc with a good understanding of clinical research and medical communication. Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills. Ability to adapt writing style to different materials and target audiences. Basic knowledge of biostatistics. Literature reviewing and evaluation capabilities. Very good working knowledge of MS Office. Application Process Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds. For this role, the process starts with a Technical Interview with the Hiring Managers, followed by a Technical Assessment, where candidates will have agreed upon timeline to complete the task.All interactions will be conducted virtually via MS Teams. Equal Opportunity Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed.We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from Anywhere As a remote-first organization, these are essential attributes we look for in all our candidates. Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently. Documenting work that brings everyone on the same page. Maturity to choose between synchronous and asynchronous collaboration. Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status. About CACTUS At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange-leveraging AI, automation, and innovation while keeping patients at the heart of everything we do. Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.