Coming Soon: Partial Sponsor Contract Clinical Research Associate – Canada
Category: CRA
Job #: Coming Soon
Utilization: 20%↑
Location: Western Canada
Job Type: 1099
Therapeutics: Oncology
One of our Sponsors is looking for a contract CRA in Western Canada with at least 20% utilization to monitor a Hema/Oncology study at a site in Alberta. Must have at least 1 year of experience monitoring Oncology and strong site management skills.
Job Responsibilities:
- Act as the "Site Manager" ensuring relationship with site(s) are positive, issues are resolved quickly, and communications are strong across all verticals.
- Assist with the development of study manuals, CRFs, monitoring standards, site study tools and other study materials as required.
- Develop and implement site recruitment, selection and initiation plan.
- Manage and drive patient recruitment and enrollment tracking.
- Provide training to sites on the study protocol, study conduct, CRF completion and data management expectations.
- Ensure essential document collection for completeness per regulatory requirements.
- Serve as a liaison with Investigators, Institutions and sites to provide support during the conduct of the clinical trial and serve as a resource for protocol and procedures.
- Demonstrate knowledge of on-site monitoring to ensure compliance with GCPs, study protocols, and SOPs. Manage one or multiple studies.
- Monitor product supplies/accountability including proper storage, dispensation, and disposal.
- Manage study completion activities including CRF collection, query resolution, record archiving and site closeout activities.
- Review in-house data and study tables.
- Mentor, coach and provide guidance to clinical staff as appropriate.
- Supervise and train other employees as appropriate.
Job Qualifications:
- Must have a minimum 3 years' recent experience as a fully dedicated Regional, Home-Based, Field Monitor for a CRO or Pharma
- Must have at least 20% utilization available
- At least 1 year of experience monitoring Oncology is required
- Strong site management skills are required
- Experience monitoring Hema/Oncology, Stem Cell Cancer, or Phase I studies is a plus
- A Bachelor's Degree and/or experience working with small to medium sized sponsors is a plus
- Must be vaccinated for COVID-19
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