Covance
Job Overview:
- Write parts of various safety reports for global regulatory submissions for Sciformixs clients, including Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Bridging reports
- Assist in writing Investigator brochures and sections of protocols
- Assist in writing Clinical Study Reports for Ph 1-4 trials, including full study reports, abbreviated reports, web synopses
- Assist pharmacovigilance teams in writing narratives for the adverse drug reactions and adverse events they process
Education/Qualifications:
- Masters degree in Pharmacy/related science area
- Bachelors degree in science
Experience:
- At least 6 months experience in the pharmaceutical industry