Associate Medical Writer
Job Description
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We are looking for a talented and detail-oriented Associate Medical Writer to join our scientific communications team. The ideal candidate will have a passion for medical writing, scientific research, and regulatory documentation, with the ability to translate complex medical data into clear, accurate, and engaging content.
Key Responsibilities:
- Create and edit clinical study reports, manuscripts, and scientific publications.
- Develop high-quality regulatory documents, including investigator brochures, protocols, and informed consent forms.
- Collaborate with medical affairs, clinical research, and regulatory affairs teams to ensure accuracy and compliance.
- Summarize and present scientific data for diverse audiences, including healthcare professionals and regulatory bodies.
- Ensure content adheres to GCP guidelines, industry standards, and client-specific requirements.
Requirements:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or related field.
- 1–3 years of experience in medical writing or scientific communications.
- Familiarity with clinical research, biostatistics, and drug development processes.
- Strong written and verbal communication skills with attention to detail.
Benefits:
- Competitive salary and benefits package.
- Opportunities to work on international medical writing projects.
- Professional development and training in regulatory writing and scientific communication.
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