Responsibilities:
Write parts of various safety reports for global regulatory submissions for Sciformix’s clients, including Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Bridging reportsAssist in writing Investigator brochures and sections of protocolsAssist in writing Clinical Study Reports for Ph 1-4 trials, including full study reports, abbreviated reports, web synopsesAssist pharmacovigilance teams in writing narratives for the adverse drug reactions and adverse events they process
Qualification:
Master’s degree in Pharmacy/related science areaBachelor’s degree in scienceAt least 6 mo
nths writing or drug safety experience in the pharmaceutical industry