Senior Clinical Data Manager
Markham, ONEverest New
5+ ansCandidates 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
Associate Director, Project Management
Markham, ONEverest New
12+ ansCandidates need a life sciences or health-related degree and 12+ years of clinical research experience in pharma, biotech or a CRO. Line management experience, strong knowledge of ICH, FDA, Health Canada and EMA rules, and excellent communication and negotiation skills are required.
Project management, Clinical research, Communication skills, Strategic planning, Tracking principles, Communicate with customers
Manager, Clinical Data and Safety Monitoring
Markham, ONEverest New
8+ ans3+ gestionEverest Clinical Research needs candidates with a graduate degree in a life science field and at least 8 years of clinical trial experience, including 5 years administering DMCs or DSMBs. They also need 3 years of people or project management, strong knowledge of GCP/ICH guidelines, and confidentiality discipline.
MS Office, Adobe Acrobat, TRS Toolbox
Clinical Operations Lead I (Oncology)
Télétravail au CanadaEverest New
7+ ansCandidates need a bachelor's degree or RN in a life science, seven years of clinical trial or monitoring experience, and thorough knowledge of ICH-GCP. Oncology experience is required, and strong leadership and a valid driver's licence are needed.
CTMS, eTMF, Trial Master File
Senior Quality Assurance Auditor
Télétravail au CanadaEverest New
6+ ansCandidates need a bachelor's degree in a health science, physics, biology or mathematics, and at least 6 years of clinical research QA experience. They must know clinical trial processes, FDA, Health Canada and EMA requirements, and ICH and GCP guidelines.
Microsoft Office
Principal PK Scientist
Télétravail au CanadaEverest New
8+ ansCandidates need a PhD in a clinical, medical or life science, or a master's with substantial experience, plus at least 8 years of PK/PD experience in pharmaceutical clinical trials. They need team leadership, strong writing skills, and proficiency in WinNonlin, NLME, Monolix or R.
WinNonlin, NLME, Monolix, Simulx, R
Clinical Research Safety Associate
Markham, ONEverest New
2+ ansEverest New needs candidates with a master's or PhD in a clinical or health field and at least two years of clinical research experience across Phase I to IV trials. Strong written and verbal communication, organization and confidentiality are required, with experience in a clinical data capture system and MS Office preferred.
MS Office, clinical data capture system