Senior Clinical Research Associate - Oncology (US, Midwest)
$97k - $193kWorldwide Clinical Trials
Worldwide Clinical Trials seeks a Senior Clinical Research Associate to manage oncology clinical trials across Midwest investigative sites. The role involves site qualification, monitoring visits, protocol compliance oversight, and study execution from initiation through closeout, with approximately 8-10 travel days monthly.
Responsibilities
- Manage clinical research activities and site performance across investigative sites
- Conduct pre-site selection, initiation, interim monitoring, and closeout visits
- Train site personnel on protocol requirements, data collection, and safety reporting
- Ensure protocol adherence, informed consent compliance, and regulatory standards
- Partner with sites and study teams to drive data quality and participant safety
Requirements
- Bachelor's degree or nursing degree
- 5+ years experience as a regional traveling Clinical Research Associate
- 2 years monitoring oncology clinical trials
- Strong knowledge of clinical trial processes and regulatory requirements
- Full-service monitoring experience preferred
- Midwest United States residency required
Compensation: $97,000–$193,000 base annually
$97k - $193k
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