Senior Clinical Research Associate - Oncology (US, Midwest)
About The Position
Worldwide Clinical Trials is hiring a home-based Senior Clinical Research Associate to support oncology clinical studies at investigative sites across the Midwest United States. The role oversees study activities from site qualification and start-up through monitoring and closeout, supporting quality, patient safety, regulatory compliance, protocol adherence, timely data collection, and reliable study data. The Senior CRA partners with investigative sites, sponsors, study teams, and global colleagues, providing site management, guidance, and oversight. Candidates must reside within the Midwest territory and should expect approximately 8–10 days of travel per month, primarily regionally, with occasional travel elsewhere as needed. The stated annual salary range is $97,000–$193,000, with final compensation based on relevant experience, performance, education, and internal equity. A competitive benefits package is offered depending on location.
Requirements
- Bachelor's degree or nursing degree.
- At least 5 years of experience as a regional, traveling Clinical Research Associate.
- At least 2 years of experience monitoring oncology clinical trials.
- Ability to travel within the specified region, approximately 8–10 days per month.
- Strong knowledge of clinical trial processes, site management, and regulatory requirements.
- Must reside in the Midwest United States territory.
Nice To Haves
- Experience in full-service monitoring.
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, including collecting regulatory documents and supporting contract and budget processes.
- Conduct Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Closeout Visits (COVs).
- Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
- Monitor site performance and provide ongoing support during study maintenance.
- Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards.
- Partner with sites and study teams to promote data quality, participant safety, and overall study success.
- Support site closeout and ensure study requirements are completed at the end of the trial.
Benefits
- Competitive benefits package, depending on location.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Senior
