Senior Director, Pharmacovigilance and Drug Safety
Markham, ONEverest New
10+ YOE5+ MgmtCandidates need a PharmD, MD, PhD or life sciences or nursing master's degree and at least 10 years of drug safety experience, including 5 in CRO leadership. They must know FDA regulations, ICH and GVP guidance, and validated safety databases such as Oracle Argus.
Oracle Argus
Clinical Safety Data Associate
Markham, ONEverest New
2+ YOEEverest Clinical Research needs candidates with an RN, MD, MSc, PhD or PharmD, or equivalent. They need two to three years of clinical trial data management experience, including medical coding and laboratory data, and strong written and oral communication.
MedDRA, WHODrug
Clinical Data Manager
Markham, ONEverest New
2+ YOEEverest Clinical Research needs a bachelor's degree in health, pharmaceutical, biological or chemistry fields with at least 2 years of clinical trial data experience, or a master's or PhD with at least 1 year. Candidates also need solid knowledge of clinical data management, regulations and standards, plus strong leadership.
Clinical research, Process data, Regulatory compliance, Project management, Quality control, Good laboratory practice
Senior Clinical Data Manager
Markham, ONEverest New
5+ YOECandidates need a bachelor's or master's degree in health, pharmaceutical, biological or chemistry sciences, and at least 5 years of pharmaceutical clinical trial data management (or 2 years as a Clinical Data Manager II). They need in-depth knowledge of clinical trial regulations and data management standards, plus proven leadership on data management projects.
EDC system
Principal Data Manager
Markham, ONEverest New
10+ YOECandidates need a master's or bachelor's degree in a related field and ten years of related experience. They must know clinical trial data management and pharmaceutical trial regulations, lead teams, and communicate clearly with all levels of staff and clients.
Electronic data capture (EDC) system