Job Title:
Clinical Regulatory Writer
Full time, Work from home but must be commutable to northern New Jersey for monthly meetings
Job Description:
- Must be available to come into the office for meetings monthly
- Minimum hours per week – 30 hours – Full 40 hours preferred
- Therapeutic focus: Immunology, Oncology, and Hematology
- Phases II-IV
Documents will include:
- Clinical Study Reports
- CTD Summary Documents
- Investigator Brochures
- Briefing books
***Submission documents are preferred. Experience in the past supporting NDA/BLA filings
Contact: Laura Walton – lwalton@aerotek.com
