286 Scientific Writing Jobs - Page 4

: 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...

We are seeking highly motivated individuals with a strong foundation in academic and scientific writing. The ideal candidate should have a solid understanding of research methodology, literature reviews, referencing styles, and publication standards. Familiarity with data analysis tools and research survey techniques will be highly valued Key Responsibilities: Create and refine academic and scientific content across disciplines Conduct thorough literature reviews and identify research gaps Develop content for research papers, review articles, surveys, and book chapters Write structured methodology and result interpretation sections Maintain accurate referencing using styles such as APA, IEEE...

Role & responsibilities: Main experience in CSR safety narratives writing (authoring, addressing review comments, collaborating with teams) Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with minimal or moderate supervision. • Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports; journal manuscripts; and abstracts, po...

The role of Scientific Writer - Content involves updating or creating scientifically and medically accurate content for commercial and medico-marketing assets such as newsletters, RTEs, social media posts, websites, digital and print brochures, banners, and more. You will be responsible for ensuring that the content for Novartis Brand/products reflects the most recent changes to Important Safety Information (ISI), Prescribing Information (PI), and other reference documents. It is crucial that these updates adhere to the stringent MLR guidelines and specifications (Medical-Legal-Regulatory). As part of the "Creative" team under Centralized Asset Support Team (CAST), you will collaborate close...

As an Intern in CMC (Formulation) at Ferring India FHPDC R&D, you will be part of the CMC (Formulation) department in Hyderabad for a duration of 12 months. Reporting to the Lead Scientist - CMC (Formulation), you will receive a stipend for your work. To qualify for this position, you should have a Masters degree in Pharmaceutical Sciences (Pharmaceutics) or a related discipline from a reputable institution. A strong academic background in pharmaceutics is essential, along with basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines such as ICH, FDA, and EMA is advantageous. Proficiency in MS Office (Word, Excel, PowerPoint) and scientific ...

The candidate should be a MSc or MTech (Bioinformatics/Computational Chemistry) graduate with 2-4 years of experience. The annual salary will be as per market standard and the location of the job is Bengaluru. As a member of the team, you will play a key role in achieving project goals for both industrial and academic projects. You will be responsible for developing creative project plans and proactively troubleshooting any problems that may arise during experiments. Core skills required for this position include knowledge and experience in Modelling, Docking, and Molecular Dynamics simulation. Additionally, you should have a basic understanding of protein structure, function, dynamics, and ...

You will be responsible for understanding the current practices, medicines, and trends in the specific therapeutic area by engaging in doctor visits, attending scientific symposia, and reviewing key therapeutic journals. This information will be crucial for providing relevant insights to both internal and external stakeholders. Your role will also involve publishing scientific articles related to company products and creating presentations for doctors, including those for Continuing Medical Education (CME) and product launches. As part of the team, you will contribute to the implementation of the medico marketing strategy and engage in field visits to doctors for product management purposes,...

Summary As a key contributor within the R&D organization at Hollister Incorporated, the Scientific Communications Writer will play a critical role in transforming complex technical data and research findings into compelling, accurate, and accessible scientific content. This individual will partner with Ostomy Technology Development and cross functional business teams to support the development of technical publications, white papers, abstracts, and internal education materials. The ideal candidate will have strong scientific acumen, data interpretation skills, publications and a solid foundation in statistics and testing methodologies commonly used in medical devices or healthcare research. ...