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.
