Delivering high-quality medical writing solutions is crucial to our success as a leading clinical research organization. As a Medical Writer, you will be responsible for creating comprehensive clinical development programs. This includes developing regulatory documents, collaborating with clients, and leveraging cutting-edge technology within the biotech sector.
Key Responsibilities:
1. Crafting Clinical Study Reports and other regulatory documents
2. Collaborating with clients and stakeholders
3. Leveraging cutting-edge technology within the biotech sector
The ideal candidate will have expertise in Clinical Study Reports and hold a relevant degree. We offer a competitive compensation package, including flexible working options and wellness initiatives.