Remote Medical Writer II/III (Pharmacovigilance)

Summary

Join PrimeVigilance, a global leader in pharmacovigilance service provision, as a Medical Writer II/III and contribute to making a positive impact in patient's lives. This role offers opportunities for career development, personal growth, and professional advancement.

Requirements

• Previous experience of pharmacovigilance medical writing, including PBRERs, DSURs, RMPs writing
• Pharmacist or MD, life science MD
• 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

Responsibilities

• 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 trainings and development, implementation and maintenance of quality system documents for medical writing, including internal templates and formats required for standardised documentation
• Support in all pharmacovigilance operations associated with medical writing
• Continuous self-education in all aspects associated with medical writing

Benefits

• Training and career development opportunities internally
• Strong emphasis on personal and professional growth
• Friendly, supportive working environment
• Opportunity to work with colleagues based all over the world, with English as the company language