Medical Writer II - Pharmacovigilance
September 27
Description
• Independent authoring, editing and reviewing of various regulatory/clinical documents • Active participation in trainings and development, implementation and maintenance of quality system documents for medical writing • Support in all pharmacovigilance operations associated with medical writing • Continuous self-education in all aspects associated with medical writing
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
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
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