Pharmacovigilance Medical Writer
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Job Summary
Seeking a detail-oriented and motivated Pharmacovigilance Medical Writer, the full-time position will involve authoring and reviewing regulatory documents, ensuring scientific accuracy and compliance, while collaborating with cross-functional teams and mentoring junior writers, all in a remote work environment.
Key Responsibilities:
- Author, review, and quality check regulatory and pharmacovigilance documents such as PSURs, PADERs, and Risk Management Plans
- Ensure documents are scientifically accurate, regulatory compliant, and delivered on time
- Act as a trusted point of contact for clients, fostering strong working relationships and supporting project delivery
Required Qualifications:
- MD, pharmacy, or Life Science degree; a Master's or PhD is desirable
- Minimum 2 years' experience in Medical Writing or related fields within a CRO environment
- Proven ability to manage multiple tasks and prioritize workload effectively
- Experience in training and mentoring Associate Medical Writers
- Fluency in English; proficiency in an additional language is a benefit
Complete Job Description
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