Job Summary:
We are seeking a highly skilled and detail-oriented Medical Writer to join our dynamic team. The ideal candidate will have expertise in writing, editing, and reviewing scientific and medical content. The Medical Writer will be responsible for transforming complex medical data and research findings into clear, accurate, and engaging documents for various audiences, including healthcare professionals, regulatory bodies, and the general public.
Key Responsibilities:
- Scientific and Medical Writing: Develop, write, and edit a wide range of documents including clinical study reports, regulatory submission documents (e.g., IND, NDA), peer-reviewed publications, and educational materials.
- Content Creation: Generate high-quality manuscripts, abstracts, posters, and presentations for scientific conferences, journals, and other outlets.
- Collaboration: Work closely with researchers, clinicians, regulatory affairs, and other stakeholders to ensure that all content meets regulatory standards, scientific accuracy, and corporate goals.
- Regulatory Submissions: Prepare and revise documents required for regulatory submissions, ensuring compliance with relevant guidelines (FDA, EMA, ICH).
- Literature Review & Research: Conduct literature searches and review existing medical research to support content development, ensuring accurate and up-to-date information.
- Quality Assurance: Edit and proofread content for clarity, consistency, accuracy, grammar, and adherence to style guides.
- Project Management: Manage timelines for multiple projects, ensuring timely and efficient completion of tasks.
- Compliance: Ensure all written materials are in compliance with medical, ethical, and regulatory standards.
Qualifications:
- Education: Bachelor’s degree in Life Sciences, Medicine, Pharmacy, or a related field. A Master’s degree or PhD is a plus.
- Experience: Minimum of 2 years of experience in medical writing, clinical research, or a related field. Experience with regulatory documents is highly preferred.
- Knowledge: Strong understanding of clinical research, medical terminology, and regulatory guidelines.
- Technical Skills: Proficiency with Microsoft Office Suite, reference management software (e.g., EndNote, RefWorks), and familiarity with medical writing software (e.g., Manuscript Manager, LaTeX).
- Communication Skills: Excellent written and verbal communication skills, with the ability to convey complex information clearly and concisely.
- Attention to Detail: Strong attention to detail with a focus on accuracy and quality.
- Collaboration: Ability to work independently and as part of a team in a fast-paced environment.
- Language Proficiency: Exceptional command of the English language. Knowledge of additional languages is a plus.
Desirable Skills:
- Experience with writing for regulatory agencies (FDA, EMA, etc.).
- Familiarity with scientific publishing and journal submission processes.
- Knowledge of Good Clinical Practice (GCP) and other relevant regulations.
- Experience with statistical analysis and interpretation of clinical data.
Job Types: Full-time, Permanent
Pay: From ₹25,000.00 per month
Benefits:
- Food provided
- Health insurance
- Provident Fund
Schedule:
- Day shift
- Fixed shift
Work Location: In person