Senior Medical Writer 🔥
Piper Clinical Solutions is actively seeking a Senior Medical Writer to join a well-established global clinical research organization (CRO). This position is 100% remote and work from home. This position can be permanent or contract depending on preference.
Responsibilities for Senior Medical Writer:
- Lead, write, review, and QC for multiple study related regulatory documents including protocols, clinical study reports (CSRs), manuscripts, informed consent forms (ICFs), and investigator brochures (IBs)
- Interpret reports, data and statistical results from clinical trials in order to write and develop manuscripts, abstracts, study reports, presentations, and posters
- Assist with editing, reviewing and QC of regulatory documents and submissions for clinical trials
- Work with cross-functional teams to ensure IND and NDA submissions are completed on time
Technical Requirements for Senior Medical Writer:
- Minimum 4 years of relevant medical writing experience for clinical research trials in a medical communication agency or clinical research organization (CRO)
- Experience as lead writer for regulatory
- Experience with multiple eCTD modules
- Strong written and verbal communication skills
-
PhD or Master's degree in biology, public health, epidemiology, or related field
Compensation & Benefits for Senior Medical Writer:
- Compensation: $120,000 – 190,000 based on previous salary history and experience
- Full Benefits: Medical, Dental, Vision, 401k, Bonus etc