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Clinical psychology Jobs in Angus, ON
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Clinical psychology • angus on
- Promoted
Clinical Research Associate (CRA) II / Senior CRA
i-Pharm ConsultingOntario, CanadaClinical Manager
The Pod GroupPeel Region, ON, CAClinical Research Associate
Piper CompaniesOntario, CanadaCoordinator, Clinical Information (Tissue)
Ontario HealthOntario Health, OntarioLead and Manager, Psychological Services
York Region District School BoardOntario, Canada- Promoted
Psychologist or Psychological Associate
Simcoe County District School BoardMidhurst, ON, CanadaField Clinical Specialist - Critical Care
Edwards LifesciencesCanada, Ontario,Clinical Specialist APV.
MedtronicOntario, CanadaPsychologist - Pediatrics, ON
Monarch Houseof our clinics in Ontario, ON, CA- Promoted
Manager, Clinical Product Development Quality Assurance
Company is ConfidentialOntario, CanadaClinical Research Associate I / II - Oncology - Toronto
ICON Strategic SolutionsOntario, CanadaIntroduction to Clinical Psychology
University of TorontoOntario, CanadaClinical Provider (Ontario, Canada)
IntellectON, CAPsychologist
Meridia Recruitment SolutionsOntario- Promoted
- New!
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Workplace OptionsON, CAClinical Research Associate (CRA) II / Senior CRA
i-Pharm ConsultingOntario, Canada- Full-time
- Permanent
Job Title : Clinical Research Associate (CRA) II / Senior CRA
Job Type : Permanent Full Time
Location : Canada
Must Have : Minimum 2 Years of On Site Monitoring Experience & 1 Year of Oncology Experience
Our client is a global leader in healthcare data, technology, and advanced analytics, dedicated to supporting the pharmaceutical and biotechnology industries in the development of ground-breaking treatments. With a strong focus on oncology, our mission is to accelerate the discovery and development of life-changing therapies. They are seeking a highly skilled Clinical Research Associate II (CRA II) to join our team and contribute to the success of cutting-edge oncology clinical trials.
Key Responsibilities :
- Oversee and manage the progress of clinical trials at investigational sites, ensuring adherence to the study protocol, ICH-GCP, and local regulatory requirements.
- Conduct site initiation, monitoring, and close-out visits, offering continuous support to ensure optimal site performance.
- Establish and maintain strong working relationships with investigators, site staff, and other key stakeholders.
- Ensure accurate and timely collection and reporting of clinical trial data.
- Proactively identify potential risks and work with the study team to resolve issues affecting timelines, data quality, or compliance.
- Provide guidance to junior CRAs and assist in their professional development.
- Ensure all clinical trial documentation is maintained in compliance with regulatory requirements and company SOPs.
- Regional travel.
Qualifications :
If you are interested in finding out more about this role or others, please contact Sharleney Chandraratna at [email protected] or call : +44 (0) 2075510732