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:
Bachelors or Masters degree in Life Sciences, Pharmacy, Medicine, or related field.
13 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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