Medical Writer III (Pharmacovigilance)

📋 Description

• Author, review, and quality check a range of regulatory and pharmacovigilance documents, including
• Ensure documents are scientifically accurate, regulatory compliant, and delivered within agreed
• Collaborate with cross-functional teams to analyse, interpret, and present safety data effectively
• Act as a trusted point of contact for clients, supporting project delivery and fostering strong
• Provide guidance, mentoring, and knowledge sharing to junior medical writers to support their
• Contribute to process improvements and the continuous enhancement of medical writing quality

🎯 Requirements

• MD, pharmacy or Life Science degree (Masters or PhD is desirable)
• Minimum 2 years' experience in Medical Writing and associated fields (case processing, signal
• Ability to manage multiple and varied tasks and prioritize workload with attention to detail
• Ability to effectively train and mentor Associate Medical Writers
• Must be a strong team player
• Fluency in English, an additional language is a benefit

🎁 Benefits

• Opportunity to make a difference by helping to bring safe and effective pharmaceutical treatment to
• Join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and
• Culture built on kindness, flexibility, growth and belonging