Clinical site monitoring expertise drives this remote Clinical Research Associate position at Parexel, supporting study quality, patient protection, and site relationships.
As a Clinical Research Associate, you will manage assigned sites from identification through close-out. You will serve as the sites' sole contact, resolve questions, and oversee delivery. The work includes qualification, initiation, monitoring, and termination visits, alongside report generation and document verification.
Key Responsibilities:
- Conduct qualification, initiation, monitoring, and termination visits
- Generate visit and contact reports for assigned clinical sites
- Build site relationships and resolve study issues
- Safeguard human subjects' rights and well-being
- Evaluate reported data, site efficacy, and drug accountability
Requirements:
- At least 18 months' direct onsite monitoring experience
- Bachelor's or equivalent degree in a health-related discipline
- Strong interpersonal, written, and verbal communication skills
- Knowledge of CTMS, EDMS, Excel, and Word
- Ability to manage multiple tasks and timelines independently
Apply clinical monitoring, communication, and quality expertise to support compliant research sites and patients through Parexel studies.
Clinical Research Associate Site Monitor in Ottawa employer: Parexel
At Parexel, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our hybrid role in Canada offers employees the flexibility to balance their professional and personal lives while providing ample opportunities for growth and development within the clinical operations field. With a strong commitment to compliance and quality, we empower our team members to make meaningful contributions to clinical trials, ensuring they feel valued and supported in their career journey.
