Senior CRA — Remote East Coast Clinical Trials Leader

Worldwide Clinical Trials Holdings, Inc.

Michigan

Hybrid

USD 97,000 - 193,000

Full time

2 days ago

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Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to ensure high-quality study conduct, patient safety, and regulatory compliance. You will lead site qualification, monitoring, and closeout activities, collaborating with sites, study teams, and sponsors to drive data integrity and study success.

This is a home-based role supporting sites across the East Coast; travel about 8–10 days per month is expected.

Qualifications

Bachelor's Degree or a Nursing Degree required.
Requires travel within the region; 8–10 days per month.
Experience in full-service monitoring preferred.
Strong knowledge of clinical trial processes and regulatory requirements.

Responsibilities

Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
Identify and assess potential research sites to support successful study execution.
Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
Conduct all types of monitoring visits: PSSVs, SIVs, IMVs and COVs.
Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
Monitor site performance and provide ongoing support throughout study maintenance activities.
Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
Partner with sites and study teams to drive data quality, participant safety, and overall study success.