Principal Biostatistician
Markham, ONEverest New
7+ ansCandidates need a PhD in statistics or a related field with at least 7 years of relevant experience, or a master's degree with at least 10 years and exceptional performance. Strong knowledge of clinical trial methodology, regulatory requirements and CDISC standards is essential.
R
Senior Biostatistician
Markham, ONEverest New
2+ ansEverest Clinical Research needs a PhD in statistics, mathematics or a related field plus 2 years of relevant experience, or a Master's degree plus 4 years. Candidates must show sustained performance in clinical research statistics.
Clinical research, Project management, Reporting, Clinical trials, Research, Statistics
Statistical Programmer I
Markham, ONEverest New
Everest New needs candidates with a Master's or PhD in statistics, biostatistics, epidemiology, public health, bioinformatics, mathematics or computer science, plus SAS Base/Advanced certification. Clinical trial programming experience is highly preferred.
SAS
Manager, Medical and Scientific Writing
Markham, ONEverest New
11+ ans2+ gestionCandidates need an advanced degree in a life or clinical science (a PhD is preferred), at least 11 years of medical writing experience in pharmaceutical or research settings, and at least 2 years managing projects or people. They also need knowledge of GCP/ICH guidelines and E3 clinical study report structure, plus strong written and oral communication.
MS Office, Adobe Acrobat, TRS Toolbox
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
Clinical Trial IWRS Monitor I
Markham, ONEverest New
3+ ansCandidates need a bachelor's degree in health science, physical or biological fields and at least 3 years of clinical trial data processing and management experience. They must work independently, communicate clearly and professionally by phone, and review data with a detailed approach.
IWRS/IRT, eDiary, CTT applications
Clinical Trial IWRS Monitor (Overnight)
Markham, ONEverest New
3+ ansCandidates need a bachelor's degree in health science, physical or biological sciences, plus at least 3 years of clinical trial data processing and management experience. Employer Everest New also wants a clear, professional telephone voice, independent work habits and a detailed approach to data review and system development.
CTT application, IWRS/IRT, eDiary
Senior Clinical Trial IWRS Monitor
Markham, ONEverest New
5+ ansCandidates need a bachelor's degree in health science, a biological or physical field, or computer science, and at least five years in clinical trial data management, with four or more years in software delivery and testing. Strong client communication, customer service, and comfort with web-based tools are also required.
SAS, IWRS/IRT, eDiary, CTT