Medical Writer Job at PrimeVigilance | Pharmacy Graduates Apply Now
PrimeVigilance (part of the Ergomed group), a specialized global pharmacovigilance provider, is seeking a Medical Writer III to join its team, with the flexibility to work remotely from Pune, India. This Medical Writer Job offers a unique opportunity to advance a career in drug safety, focusing on the independent authoring, editing, and reviewing of various regulatory/clinical documents. Essential experience includes pharmacovigilance medical writing, particularly for PBRERs, DSURs, and RMPs (Risk Management Plans). For this Pharmacy Job, candidates must hold a Pharmacy, Medicine, or advanced Life Science degree and possess the ability to manage and mentor junior writers. To work efficiently, finding the ideal medical writer job is crucial.
- Job Post: Medical Writer III
- Location: Pune, India
About The Company
PrimeVigilance, part of the Ergomed group, is a specialized mid-size global pharmacovigilance service provider established in 2008. The company has achieved global organic growth, offering comprehensive services in Pharmacovigilance, Medical Information, Regulatory Affairs, and Quality Assurance across Europe, North America, and Asia. PrimeVigilance is dedicated to supporting pharmaceutical and biotechnology partners and places strong value on employee experience, offering excellent training, development, and a supportive environment for staff to deliver high-quality client service. The pursuit of a rewarding Medical Writer Job can find fulfillment here.
Qualifications
- Previous experience in pharmacovigilance medical writing, including PBRERs, DSURs, and RMPs writing
- Pharmacy degree
- Ability to manage multiple and varied tasks and prioritize workload with attention to detail
- Ability to effectively train and mentor Associate Medical Writers
- Advanced knowledge of English is required for the Pharmacy Job
Key Responsibilities of the Medical Writer Job
- Independent authoring, editing, and reviewing of various regulatory/clinical documents (e.g., aggregate reports, risk management plans and other documents needed throughout the product’s life cycle) with the responsibility for the quality and content of the document and compliance with internal and external standards
- Active participation in training and development, implementation and maintenance of quality system documents for medical writing, including internal templates and formats required for standardised documentation. This role elevates your career in the medical writer job field.
- Support in all pharmacovigilance operations associated with medical writing
- Continuous self-education in all aspects associated with medical writing
- Managing a team of junior medical writers
