Conduct and report SIV, RMV, COV onsite monitoring visits.
Perform CRF review, source document verification, and query resolution.
Manage site communication and act as point of contact for in-house support and vendors.

Qualifications:

College/University degree in Life Sciences or equivalent combination.
Independent on-site monitoring experience with Phase II and/or III trials.
Full proficiency in English and French; MS Office skills.

Work Environment:

Dynamic team environment requiring ability to plan, multitask, and problem-solve.
Travel required with valid driver's license.
Opportunity to develop skills and widen therapeutic area experience.

Full-Time

The company is a dynamic, global mid-size clinical research organization founded in 1995, bringing together more than 3,000 dedicated individuals. They work on the frontline of medical science, changing lives and bringing new medicines to those who need them.

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