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ICON plc
Overview
Accountable for site selection and study start-up activities for Phase I-IV trials, ensuring timelines and deliverables are met. Manages regulatory submissions, site documentation, and financial contracts to achieve site greenlight.
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Compensation
Salary not listed
Posted
3 days ago
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
8 days ago
The Salvation Army Canada and Bermuda Territory
Provide comprehensive case management, supervision, and support for residents of the Halifax Centre of Hope and the Anchorage Recovery Program. Facilitate group counselling, conduct intakes, and implement therapeutic modalities to support clients with substance use disorders.
CA$21 - CA$32 / HOUR
Fortrea
The role involves managing all aspects of clinical site monitoring, including initiation, routine visits, and close-out for oncology trials. Key duties include ensuring patient safety, verifying informed consent, and maintaining data integrity through CRF review and SAE reporting.
9 days ago
Coordinate the setup and monitoring of oncology clinical trials while maintaining accurate study documentation and reports. Build collaborative relationships with investigators and site staff to ensure patient safety and regulatory compliance.
15 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 conducted, recorded, and reported according to SOPs and ICH-GCP standards.
CA$108,576 - CA$135,720 / YEAR
17 days ago
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.
AstraZeneca
The Clinical Research Associate (CRA) is responsible for the local delivery of clinical studies at assigned sites, acting as the main contact for monitoring study conduct to ensure proper delivery according to guidelines and regulations. This involves preparing, initiating, monitoring, and closing assigned sites, training site staff, driving site performance, and ensuring data quality and compliance.
CA$109,149 - CA$143,258 / YEAR
23 days ago
Fraser Health
The LPN provides direct nursing care and administers Transcranial Magnetic Stimulation (TMS) treatment for clients with treatment-resistant depression. Responsibilities include performing psychosocial screenings, monitoring patient responses, and coordinating care with an interdisciplinary team.
CA$33 - CA$45 / HOUR
1 month ago
VetStrategy / Daubigny
Provide high-standard veterinary care and perform surgeries for patients at Cranberry Hill Animal Hospital. Build and maintain strong, trusting relationships with clients and the local Kemptville community.
Provide high-standard veterinary care and perform surgeries for patients at Cranberry Hill Animal Hospital. Build and maintain strong, trusting relationships with clients and engage in community-oriented activities.
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management. Ensures the protection of study patients and the integrity of data submitted on Case Report Forms.
dentalcorp
The role involves clinical chairside assisting duties and establishing strong patient relationships while adhering to ethical professional behavior. Additionally, the assistant is responsible for preparing treatment rooms in accordance with infection control protocols.
The veterinarian will play an active role in delivering exceptional care across a wide range of cases, including preventative medicine, surgery, and dental care. This role requires supporting clients with compassion and clear communication while collaborating with a skilled team.
2 months ago
The veterinarian will play an active role in delivering exceptional care across a wide range of cases, including preventative medicine, surgery, and dental care. Responsibilities also include supporting clients with compassion and clear communication.
The Clinical Research Associate is locally responsible for study delivery at assigned sites, acting as the main contact to monitor study conduct, ensuring compliance with AZ procedures and international guidelines like ICH-GCP. Key tasks include preparing, initiating, monitoring, and closing sites, training site staff, driving site performance, and ensuring timely data quality and reporting.
3 months ago
IQVIA
The role involves performing monitoring and site management tasks for various clinical protocols, therapeutic areas, and sites, including conducting site visits (selection, initiation, monitoring, and close-out) according to contractual scope and regulatory guidelines. Key duties include managing protocol training, tracking study progress, ensuring data quality and integrity, and maintaining essential study documentation like the TMF and ISF.
CA$102,500 - CA$170,900 / YEAR
