As a Medical Writer, you will be responsible for ensuring timely, clear, and proactive communication and collaboration with stakeholders and colleagues globally. This role involves:

• Communicating across different time zones and professional environments.
• Planning and managing your work to meet timelines.
• Challenging expert contributors to improve the quality of their written contributions.
• Frequent traveling abroad for meetings, conferences, and courses.

Key Responsibilities:

• Ensure timely, clear, and proactive communication and collaboration with global stakeholders.
• Contribute to process improvements, knowledge sharing, and skill building.
• Mentor and train other medical writers as needed.
• Plan and manage variable workloads, seeking help and advice when needed.
• Attend meetings and conferences abroad to stay updated with global standards and practices.

Qualifications:

• Graduate degree (PhD, MSc, M Pharm, or equivalent).
• 4+ years of experience as a medical writer or in a relevant role.
• Experience working within a global setting and in the pharmaceutical/CRO industry.
• Strong understanding of regulatory document requirements.
• Excellent communication and analytical skills.
• Ability to work independently and manage variable workloads.
• Commitment, persistence, and accountability.

Application Link