Credevo
Website:
credevo.com
Job details:
Job Title: Medical Writer
Location: Remote
Job Type: Full-time
Experience: 3-5 years in medical writing, regulatory writing, or related field
Industry: Clinical Research, Pharmaceuticals, Healthcare.
Job Summary:
We are looking for a skilled Medical Writer to create accurate, engaging, and
regulatory-compliant medical content. The ideal candidate will be responsible for writing
scientific documents, clinical study reports, regulatory submissions, and other medical
communications for clinical trials and pharmaceutical companies.
Key Responsibilities:
● Develop and write high-quality clinical study reports (CSRs), protocols, SOPs,
Articles, Blogs, investigator brochures (IBs), regulatory submissions, and
scientific publications.
● Prepare manuscripts, white papers, literature reviews, and abstracts for journals
and conferences.
● Collaborate with cross-functional teams, including clinical research, regulatory affairs,
and biostatistics.
● Ensure compliance with ICH-GCP, regulatory guidelines (FDA, EMA, ICMR), and
industry standards.
● Conduct extensive literature reviews and summarize scientific data effectively.
● Edit and proofread medical content to ensure clarity, accuracy, and consistency.
● Support the development of medical and scientific training materials.
● Stay updated with latest industry trends, drug development processes, and clinical
research advancements.
Qualifications & Skills:
● Bachelor’s in Life Sciences, Pharmacy, Medicine, Biotechnology, or a related field.
● 3 - 5 years of experience in medical writing, clinical research, or pharmaceutical regulatory documentation.
● Strong understanding of clinical trials, medical terminology, and regulatory requirements.
● Excellent written and verbal communication skills.
● Proficiency in MS Office (Word, Excel, PowerPoint) and reference management tools.
● Ability to interpret and analyze scientific data and present it effectively.
● Can write SEO friendly articles & blogs
● Detail-oriented, highly organized, and capable of working independently and in teams.
Preferred Qualifications:
● Familiarity with publication guidelines (ICMJE, GPP3).
● Prior experience with regulatory writing (IND, NDA, CSR, CTD modules, etc.). Why Join Us?
● Opportunity to work with leading experts in clinical research and pharmaceuticals.
● Exposure to global clinical trial documentation and regulatory writing.
● A dynamic and growth-driven work environment with career advancement
Interested candidates kindly share their resume on kanishka.t@credevo.com or hr@credevo.com
Click on Apply to know more.