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AbCelleraNew
Overview
The role involves designing and executing in vitro and in vivo toxicology studies to assess the safety of drug candidates. Responsibilities include maintaining GLP-compliant data and authoring toxicology sections for regulatory documentation.
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Compensation
CA$100,000 - CA$125,000 / YEAR
Posted
New
Lead the design and oversight of in vitro and in vivo toxicology studies to assess the safety of drug candidates. Serve as a subject matter expert for nonclinical safety, authoring regulatory documentation and providing risk-benefit evaluations to leadership.
CA$112,000 - CA$150,000 / YEAR
Indero
The Senior CRA monitors clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP guidelines. Responsibilities include conducting site visits, performing source data verification, and potentially mentoring other CRAs as a Lead CRA.
Salary not listed
8 days ago
AbCellera
Perform daily animal health assessments, cage changes, and maintain the cleanliness and organization of the in vivo facility. Support the discovery of therapeutic antibodies by preparing lab materials and managing sample shipments.
CA$52,700 - CA$62,000 / YEAR
14 days ago
The In Vivo Specialist will perform in vivo and ex vivo techniques to support therapeutic antibody discovery and efficacy assessments. They are responsible for maintaining high standards of animal welfare, accurate data documentation, and ensuring efficient study execution.
CA$75,800 - CA$94,700 / YEAR
16 days ago
The Senior CRA conducts site qualification, initiation, monitoring, and close-out visits to ensure clinical trials adhere to protocols and regulatory standards. They also build relationships with investigators, perform source data verification, and may mentor other CRAs while overseeing site metrics.
ICON plc
The Senior Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are accurately conducted, recorded, and reported according to SOPs and ICH-GCP standards.
CA$108,576 - CA$135,720 / YEAR
17 days ago
The Senior Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are accurately recorded and reported in accordance with ICH-GCP and standard operating procedures.
Monitor the progress of clinical studies at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. Maintain accurate records and reports in accordance with ICH-GCP and standard operating procedures.
GSK
The student will support the Quality Control department by managing the archiving and circulation of GMP documents. They will also act as an administrator for the eSOP system and assist users with document layout and technical issues.
1 month ago
The student will support the Quality Control department by managing document archiving, circulation, and identification within the documentation center. They will also act as an administrator for the eSOP system and assist users with document formatting and compliance.
Novir
Administer vaccinations in onsite clinic settings while providing compassionate care to residents. Assist with clinic operations, including setup, breakdown, and accurate documentation in the EMR platform.
CA$21 - CA$26 / HOUR
Sygnature Discovery
The Research Associate will design and execute efficient multi-step organic syntheses to support drug discovery projects. They are responsible for purifying and characterizing compounds while maintaining accurate laboratory records and adhering to safety standards.
CA$55,000 - CA$70,000 / YEAR
Everest Clinical Research
The Clinical Trial Assistant will interact with sponsors, sites, and vendors to ensure timely and high-quality operationalization of clinical trials while compiling and reviewing documentation for site qualification and regulatory submissions. Responsibilities also include setting up, maintaining, and archiving essential documents in the Trial Master File (TMF) and Clinical Trial Management System (CTMS).
CA$45,000 - CA$65,000 / YEAR
2 months ago
The Medical Writer will perform internal Quality Control (QC) procedures for various clinical documents and act as a lead writer in preparing clinical documents or scientific publications, adhering to established timelines and styles. Responsibilities also include performing literature searches, document e-publishing, and potentially serving as a Data Monitoring Committee (DMC) Administrator or Secretary.
CA$65,000 - CA$100,000 / YEAR
4 months ago
