Impactful On-Site Clinical Research Coordinator; Temp

Tekton Research seeks a Clinical Research Coordinator (CRC) for a temporary, on-site role in Fort Collins, CO. The CRC will manage study start-up to close-out, coordinate enrollment, and oversee data integrity while ensuring GCP and FDA compliance.

Responsibilities include regulatory submissions (IRB), adverse event reporting, and collaboration with investigators and sponsors to ensure smooth trial conduct. Strong organizational and communication skills are essential.

The following role is for a Impactful On-Site Clinical Research Coordinator (Temp) with Tekton Research.

We aim to respond to suitable candidates as soon as possible.

Full responsibilities and requirements are described in the listing above.

Learn more about the Impactful On-Site Clinical Research Coordinator (Temp) role in the description above.

We appreciate your interest in this position.

Join Tekton Research and contribute to our ongoing work.