Sr Medical Writer, Regulatory at Pharmaceutical Product Development (PPD)

Our writers possess strong leadership and project management skills, are creative problem solvers and decision makers, are engaging mentors and enthusiastic members of the department with an eagerness to continually improve our offerings and deliver a market leading service to our clients. In return, the medical writing department offers a highly competitive compensation package together with excellent opportunities for personal development and progression within the field. All within a friendly, fast paced and exciting environment.

The Medical Writer collaborates with internal and sponsor team members to interpret, distill, and summarize complex data concepts. Other tasks include presentation of clinical messages in clinical study reports, summarization of preclinical and clinical studies for preparation of investigator's brochures, and referencing current research and regulatory guidelines for preparation of protocols. Their work documenting clinical study trials covers a wide range of therapeutic indications.

You will be a part of a team who is dedicated to its people and foster a supportive, collaborative culture based on trust, flexibility and work life balance. 

Job Qualification

Qualifications required:

• Education to Bachelor’s/advanced degree level in a scientific discipline
• 5+ years of experience within regulatory medical writing
• Excellent grammatical, editorial and proofreading skills