Senior Clinical Research Associate

ClinChoice is a global, full-service CRO providing clinical research services to pharmaceutical, biotechnology, medical device and consumer health companies. We are currently seeking an experienced Senior Clinical Research Associate (Senior CRA) to join our in-house team.

As a Senior CRA, you will manage 2–3 clinical trials and be responsible for site management activities, including study start-up, site monitoring, and closeout. You'll conduct both on-site and remote monitoring while supporting a variety of studies across a diverse client portfolio, from emerging biotech companies to large pharmaceutical organizations.

This is a permanent, fully remote position. Candidates must be willing and able to travel to investigative sites as needed.

Candidates must have experience monitoring oncology and other complex clinical trials, as well as previous experience working for a CRO. A strong understanding of GCP, ICH guidelines, and clinical trial operations is also required.

Join our team: you can be part of making a difference in people’s lives and experience a fulfilling and rewarding career!

This is a remote role, ideal locations are West Coast, Northeast and/or Florida.

• Keep professionally abreast of all scientific, regulatory and operational aspects relevant to the clinical projects assigned.

• Assist in the selection of sites, site evaluation visits, initiation visits and ensure follow-up by obtaining pre-study documentation to ensure good start-up of the investigation sites.

• May act as Feasibility Associate.

• Train site staff in all study procedures.

• Conduct periodic monitoring visits, including completion of monitoring visit report. Review at each visit the accuracy, legibility, completeness and quality of the Case Report Forms (CRF).

• Conduct source data verification and in-house review of clinical data and ensure timely resolution of data queries to guarantee reliable clinical data.

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