Job Description

Clinical Research Associate (Minneapolis, MN)

The Opportunity:

My client is a rapidly growing CRO, with a passion in bringing successful life changing therapies to critically ill patients across the globe.

Great team and management with a real process in place for contractors to be part of the team and valued.

We are currently hiring a Clinical Research Associate, for a contract role with the possibility of becoming permanent, who must be located in Minneapolis, Minnesota.

Key Responsibilities:

• Serve as the primary liaison between study sites and the sponsor, ensuring smooth communication and collaboration.
• Conduct site initiation, routine monitoring, and study close-out visits while maintaining accurate and compliant documentation.
• Expand knowledge across diverse therapeutic areas by working on a variety of clinical trials.
• Oversee study compliance with Good Clinical Practice (GCP), protocols, and regulatory requirements.
• Assist in the development and review of study protocols and related documentation.
• Prepare and submit ethics applications and contribute to Clinical Study Report preparation.

Desired Experience:

• A degree in life sciences, healthcare, or a related field.
• 5+ years of experience as a Senior CRA within a life science organization.
• In depth knowledge of ICH, GCP Guidelines and FDA regulations.
• Oncology experience is highly desirable.
• Must be open to travel – will most likely be regional.

If you are interested, get in touch with me ASAP by simply applying.

You can also send your most up to date CV directly to me, and I will reach out to you.

Jean-David Mandarin – Clinical Associate Recruiter

Email – [email protected]

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