Job Description

Overview:

We are seeking a detail-oriented and experienced

Medical Writer

to join our team. The ideal candidate will have a strong background in scientific writing and a deep understanding of medical and healthcare concepts. You will work closely with cross-functional teams to create high-quality documents for clinical trials, regulatory submissions, publications, and other scientific materials.

Key Responsibilities:

Write and edit medical and scientific documents, including clinical study reports, regulatory submissions, research papers, and more. Ensure clarity, accuracy, and compliance with regulatory requirements and company standards. Collaborate with researchers, clinicians, and regulatory professionals to gather necessary information. Stay updated on industry standards, medical literature, and regulatory guidelines. Provide scientific input to ensure all documents are aligned with project goals and target audiences.

Qualifications:

Degree in Biotechnology, Pharm-D or other relevant degrees. Proven experience as a Medical Writer in the healthcare or pharmaceutical industry. Strong writing, editing, and proofreading skills. Familiarity with medical terminology, clinical research processes, and regulatory guidelines. Ability to work independently and meet deadlines in a fast-paced environment. Excellent communication and collaboration skills.
Job Type: Full-time

Pay: ?15,000.00 - ?30,000.00 per month

Schedule:

Day shift
Work Location: In person