518 Scientific Writing Jobs - Page 13

Overview If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Associate Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Please Note: CactusLife Sciences is a remote-first organization and we embrace an accelerate from anywhere culture. You may be required to travel to our Mumbai office based on business requirements or for company/team events. Responsibilities Use scientific expertise to develop high-quality, publication-ready scientific documents for SciComms and Medical Information clientele, including MSL slid...

About Orica At Orica, its the power of our people that leads change and shapes our futures Every day, all around the world, our people help mobilise vital resources essential to progress Established in 1874, we have grown to become the world leader in mining and civil blasting with a diverse of team of more than 13,000 across the world, Its an exciting time to join us we are shaping the future of mining through digital and automated technologies, embracing new ways of thinking, pioneering innovation and reimagining the way we work, About the role Orica is looking for an Accounting Analyst Financial Controls to be based in our Hyderabad office Youll be at the heart of our financial operations...

We are looking for a dynamic and proactive medical writer with exceptional communication skills and a strong foundation in clinical research. In this pivotal role, you will play a key part in critically analyzing and summarizing complex medical literature to extract valuable insights. Your collaboration with cross-functional teams will be integral to the systematic review of medical literature, ensuring that our reports meet stringent standards and regulatory guidelines. Join our team and contribute to our commitment to excellence in the dynamic field of medical writing and literature analysis. Independently plan, write, edit, and format literature review study protocols, scientific manuscri...

You will be joining Be Clinical, a company dedicated to creating a science-backed, clinical-grade, anti-aging skincare brand tailored for the modern Indian consumer. Your role as a Scientific Researcher in New Delhi will involve conducting laboratory experiments, writing research papers, collaborating with fellow scientists, and innovating new skincare formulations. Working closely with the product development team, you will ensure that all products meet clinical standards and deliver effective results. To excel in this role, you should possess laboratory experience, skills in experimental design and data analysis, scientific writing proficiency, and a knack for research paper publication. K...

The University of Glasgow is seeking a dedicated individual to join the LISA Optical Bench Team. In this role, you will be responsible for working on the optical benches that are crucial components of the interferometry system on spacecraft. The optical benches are constructed using Zerodur, a low expansion glass, with precise alignment of optical components. Your tasks will include designing, building, testing, and documenting various subsystems such as beam collimators, imaging systems, and beam dumps that are integrated into the optical benches. A key aspect of this position involves collaborating with a diverse range of partners, including sub-system suppliers from multiple European coun...

UMEDICA is a vertically integrated company engaged in the manufacturing and export of a wide range of finished formulations including Injectables, Tablets, Capsules, Suspensions, Dry Syrups, etc. Our manufacturing facility, situated in Vapi (Gujarat), holds approval from global regulatory authorities. Founded in 1983, UMEDICA operates in over 85 countries across the globe, encompassing EU, UK, USA, Canada, Australia, Middle East, Central & South American countries, Africa, Asia & CIS countries. Upholding a culture of innovation & continuous improvement, we at UMEDICA constantly strive for excellence. We are currently looking for a dynamic and experienced Manager/ Sr. Manager specializing in ...

About the Role: We are seeking an experienced and strategic Medical Affairs Lead. The ideal candidate will be a post-graduate (MD) in Pharmacology with a strong background in medical affairs, medico-marketing, and clinical research within the Nutrition, Pharmaceutical or Consumer Healthcare industries. This role requires a professional with a proven track record of leading medical and scientific affairs, driving innovation, and engaging with key scientific leaders and stakeholders. Key Responsibilities: Lead and execute medical and scientific affairs initiatives, ensuring alignment with global scientific communication strategies. Act as a Medical Subject Matter Expert (SME) for adult nutriti...

: Generating new ideas and identifying areas of research from cell and molecular biology research Working on cell-based and non-cell-based assays for large molecules, peptides, ADCs. Performing molecular biology experiments as per project requirement at CRO or in-house lab Scientific writing related activities such as manuscript, grant writing etc. To support in data processing and compilation of all in-vitro/in-vivo data generated in-house or received from service provider. Literature review as per project requirement. Required Skills: Cell-Based Assays | Advanced Non-Cell-Based Assays | Advanced Molecular Biology Techniques | Intermediate Data Processing & Compilation | Advanced Scientific...

: Designing and execution of cell and molecular based, enzymatic biochemical, and analytical MD and MV for current ongoing/upcoming projects. Responsible for management of extensive literature review, reports review, and method development for in-vitro cell and molecular biology activities pertaining to new product pipeline. Supervision of in-vitro activities conducted inhouse and externally at CRO. Data management, compilation, analysis, interpretation, summation, and documentation of the data across the projects. Planning, and collaboration for the ongoing/upcoming projects across the India and globally. Required Skills: Cell and Molecular Biology Techniques | Expert Biochemical & Enzymati...

Clove Dental is looking for Periodontist to join our dynamic team and embark on a rewarding career journey Periodontist is responsible for various tasks including planning, execution, and management of related duties They should possess relevant skills and experience to excel in this role Duties include teamwork, problem-solving, and achieving organizational goals Candidates must have strong communication and technical abilities Responsibilities include project management, strategy execution, and performance optimization (More details as per role requirements )

Ghintell (www.ghintell.com) is a research and analytics company of the Zealth Group, Denmark MNC (www.zealthcon.com), which supports global pharmaceutical and biotech clients in their goal to bring their products to patients by providing advisory and consulting in areas such as market access, pricing & reimbursement, HTA submissions, medical reviews, disease and market landscapes, forecasting, marketing and commercial analytics, business intelligence, marketing communications, medical education and digital development etc. Ghintell believes in the following Core Values that are cornerstone of our existence. Customer satisfaction: We meet and exceed our customers expectations. Candor: We spea...

Responsibilities: Prepare clinical study reports, protocols & newsletters Design medical affairs strategies Conduct literature reviews & ICH compliance checks Write scientific documents with CRF & KOL input Protocols, abstracts, posters, manuscripts Provident fund

If interested, share your CV at [HIDDEN TEXT] or 9036659658 Position: Head of Medical Affairs & Content Location: Mumbai (Andheri West) Department: Medical Affairs | Scientific Strategy | Content Development Experience: 812 years Salary: Upto 15 LPA About The Company: This is a leading medical communications company serving top pharmaceutical brands, specialized in scientific content, digital education, and medical events. They are expanding into doctor-facing knowledge portals to deliver real-time clinical updates, and were looking for a dynamic Senior Content Manager to help lead this growth. Role Overview: Seeking a visionary Head of Medical Affairs & Content to lead the scientific and co...

Medical & Pharmacological Writing: Manuscripts, conference abstracts, Marketing collateral, digital content Medical scripts for videos & multimedia projects Research & Analysis: scientific literature reviews Quality Control Cross-Team Collaboration Required Candidate profile Skilled & motivated Medical Writer to develop high-quality scientific content for our pharma clients. Translating complex data into clear, accurate & compelling materials across various formats

Role & responsibilities Prepare clinical study report of BABE studies and patient based clinical trial studies (PK end point/PD end point/clinical end point studies) on the basis of data received from clinic after completion of study as per regulatory requirement/SOPs/client standards/client approved templates. Final compilation of the project report with respected appendices as per e-CTD including Module 2 (Summary report) and Module 5(Compilation of study report, literature, appendices & BR report) and/or applicable regulatory guidelines & requirements. Submit final compilation signed report with e-CTD to client. Co-ordinate with Project Manager for report requirement, sponsor's comments &...

Create evidence-based medical content (Medico-marketing collaterals, manuscripts, protocols, patient materials, etc.Collaborate with experts and teams for information. Review and edit content.

SUMMARY SAR & SAR-like Patient Safety Physician Job Description Responsible for compiling PBRERs with a focus on medical aspects and safety sections of products, and analyzing safety trends, including source data analysis based on queries Assisting in identifying, analyzing, and drawing conclusions from safety data for cumulative trends Collaborating with Therapeutic Head to identify signals and address product safety concerns Engaging with Therapeutic Area colleagues for enhanced understanding and development Measurable Goals Ensuring 100% compliance with timely completion of all client and Cognizant required trainings Achieving 100% compliance with work allocation plan, including case clos...

Review of promotional and medical communication materials (for various client products) and ensure the content in these materials is medically accurate, scientifically rigorous, truthful and balanced, relevant to product and therapy area, compliant to various pharma regulations and guidelines and is supported by authentic and up to date references. Develop and update content for various medical materials, perform literature search to identify appropriate references to support creation/update of scientific content, track and audit assets for various purposes. Develop and review content for various deliverables meeting quality requirements as per client satisfaction metrics, within assigned ti...

Seeking a dynamic leader to drive clinical content strategy, overseeing both commercial and non-commercial scientific content for HCP engagement. Responsible for ensuring accuracy, compliance, and innovation in medical writing across multiple formats. Key Responsibilities Lead and manage a team of medical writers, editors, and researchers. Oversee the creation of scientific, educational, and promotional content. Ensure content integrity, regulatory compliance, and editorial excellence. Collaborate with KOLs, medical societies, and internal teams. Drive innovation in digital content and AI-driven solutions. Qualifications & Skills Advanced degree (MD, PhD, MBBS, MPharm, etc.). 5 years in medi...

Medical Writer Location : RRD - Chennai ( Work from Office) No of positions : 2 In this role you will be responsible for: Developing clear, concise, and scientifically accurate medical documents and marketing collateral, including presentations, whitepapers, video scripts, flashcards, brochures, and more. Creating audience-appropriate medical content for patients, healthcare professionals, regulatory agencies, and internal stakeholders. Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards across all content formats mentioned above. Collaborating with subject matter experts, scientists, and regulatory teams to develop compelling...

Manage DNA Slim protocol, medical reviews & reporting Oversee slimming programs and supervise the team Drive team performance, event participation, and client conversions Ensure scientific planning and tracking of each clientjourney

Role & responsibilities - Content Development: Write, edit, and proofread scientific manuscripts, research articles, review papers, grant proposals, and technical documents. Communication: Translate complex scientific data and concepts into clear, engaging, and accessible content for a variety of audiences. Collaboration: Work closely with researchers, scientists, and subject matter experts to gather information, verify accuracy, and ensure clarity of scientific content. Publication Management: Assist in the preparation and submission of manuscripts to peer-reviewed journals, including managing revisions and responding to reviewers' comments. Support: Develop scientific content for marketing...

1. JOB PURPOSE Join Clinical Development, Clinical Operations, Biometrics, Medical Affairs, and Pharmacovigilance teams to advance gene & cell therapy programs from Phase IIII. Unique opportunity to bridge clinical science and business strategy in a fast-paced biotech environment. Join Ocugen’s Clinical organization (Clinical Development, Clinical Operations, Biometrics, Medical Affairs, and Pharmacovigilance) to contribute across the full spectrum of drug development in gene and cell therapies. 2. DUTIES AND RESPONSIBILITIES Support protocol development, amendments, IB/ICF creation, and regulatory submissions (INDs, BLAs, CTAs). Participate in medical monitoring: eligibility review, safety ...

Role: Sr.Medical Writer Location: Chennai/WFH Shift: Rotational Shift Senior Medical Writer for its Creative Communications team. In this role you will be responsible for: Developing clear, concise, and scientifically accurate medical documents and marketing collateral, including presentations, whitepapers, video scripts, flashcards, brochures, and more. Creating audience-appropriate medical content for patients, healthcare professionals, regulatory agencies, and internal stakeholders. Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards across all content formats mentioned above. Collaborating with subject matter experts, scie...

Environmental Surveillance of respiratory virues and other pathogens to genomic diversity of pathogens and microbiome in wastewater. Using spatial and temporal information on environmental samples and disease incidence, we want to identify regionally prevalent variants for an early indication of infection trends. The role will be to provide bioinformatics support using available software packages (commercial and open access) to underpin the processing, analysis and visualisation of genomic data arising from sewage (wastewater) using a combination bioinformatics and statistical approaches. Number of vacancies: 1 position Age limit: 35 years as on 01.07.2025 Duration Initially, the position wi...