Tasks

- Compose, write, and edit medical writing deliverables covering all phases of clinical research for submission to regulatory agencies
- Be in contact with clinical teams to understand the nature of the scientific work that they will be covering
- Deliver clinical documents including comprehensive CSS, CSP, annual reports, investigator brochures, etc.
- Attend meetings and support assigned therapeutic area publication team in manuscript and/or publications submissions to scientific meetings, medical journals
- Manage document development timelines to facilitate timely submission

Qualifications

- Bachelor’s degree in life sciences; Masters, PhD, PharmD would be a plus
- At least 3-5 years of experience in the pharmaceutical or related industry
- Oncology and/or Non-Oncology (cardiovascular, respiratory and immunology) publication writing experience specific to CSS, CSP, CSR, IP, and regulatory package documentation
- Business fluent in English written and spoken