If youโre aiming to build a career in medical writing, scientific communication, and publication support, this Senior Medical Writer job at Apcer Life Sciences offers a strong opportunity. With demand rising for professionals skilled in clinical research writing, literature review, and regulatory-compliant documentation, this role positions you at the core of scientific content development in the pharmaceutical industry.
This opening is ideal for candidates with 2โ5 years of experience in medical and scientific writing, particularly those experienced with PubMed, Embase, Cochrane databases, and manuscript development.
๐ Job Overview
- Role: Senior Medical Writer
- Company: Apcer Life Sciences
- Location: Ahmedabad, Noida
- Experience: 2โ5 Years
- Employment Type: Full-Time, Permanent
- Industry: Pharmaceutical & Life Sciences
๐ Key Responsibilities
As a Senior Medical Writer in India, your responsibilities will include:
- Developing high-quality scientific and medical content across therapeutic areas
- Conducting in-depth literature reviews using databases like PubMed, Embase, and Cochrane
- Drafting and reviewing:
- Manuscripts
- Abstracts & posters
- Slide decks & newsletters
- Infographics & medical education materials
- Supporting manuscript submission and journal publication processes
- Ensuring quality control, scientific accuracy, and regulatory compliance
- Editing, proofreading, and verifying references for scientific documents
- Collaborating with clinical, regulatory, biostatistics, and marketing teams
- Managing project timelines, deliverables, and document version control
- Interacting with clients and stakeholders to meet project expectations
๐ Qualifications & Skills
To qualify for this medical writing job in India, candidates should have:
- M.Pharm / Postgraduate / Ph.D. in Life Sciences or Pharmaceutical Sciences
- 2โ4 years of experience in medical or scientific writing
- Strong expertise in:
- Scientific writing tools
- MS Word, Excel, PowerPoint
- Excellent written and verbal communication skills
- Knowledge of publication standards, SOPs, and ethical guidelines
- Experience in clinical research documentation and medical communications
๐ผ Why Consider This Role?
- Opportunity to work in global scientific publications and medical communications
- Exposure to cross-functional collaboration with clinical and regulatory teams
- Career growth in pharmacovigilance, clinical research, and regulatory writing
- Work on high-impact scientific content and journal submissions
๐ How to Apply
