Location : Quebec or Ontario
Status: 1 Regular Full Time & 1 Temporary Full Time (2 year)
The Clinical Research Associate II is responsible for the identification, evaluation, selection, initiation, monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards.
The Clinical Research Associate II role is accountable for clinical trial monitoring and managing investigator site relationships to ensure effective delivery of clinical trials (e.g. site activation, enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site health), to maintain investigator and site staff engagement and satisfaction, and to enhance the company's image with its external stakeholders.
The Clinical Research Associate II is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with study team members as required in activities associated with the set-up, running and close out of a clinical trial.
Clinical Trial Monitoring
Clinical/Scientific and Site Monitoring Risk:
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS:
Pfizer is an equal opportunity employer and encourages women, Aboriginal people, persons with disabilities and members of visible minorities to apply. Pfizer will accommodate the needs of applicants with disabilities throughout all stages of the selection process. Should accommodation during the recruitment process be required, please advise your Talent Acquisition representative.