Senior Clinical Research Associate - 177466

Responsibilities: of the Senior Clinical Research Associate include: · Independently manage site monitoring activities for Phase II and III oncology trials, including a combination of onsite and remote visits averaging 8-10 onsite days per month. · Serve as the primary clinical contact for assigned sites, building strong, long-term relationships and providing consistent support and guidance. · Ensure study conduct aligns with protocol requirements, GCP, ICH guidelines, and applicable regulatory standards. · Oversee site performance, data quality, and issue resolution while proactively identifying and mitigating risks. · Prepare accurate and timely monitoring documentation, including visit reports and follow-up communications. Qualifications: for the Senior Clinical Research Associate include: · Minimum of 2+ years of oncology monitoring experience with current expectations of approximately 3 years of independent monitoring. · Hands-on experience supporting Phase II and Phase III clinical trials, ideally within a full-service model working with biotechnology clients. · Ability to operate autonomously, including serving as the sole CRA on a study and managing site relationships with minimal oversight. · Willingness and ability to travel regionally, reside within one hour of a major airport, and maintain required onsite visit expectations. · Bachelor's degree not required for senior-level consideration if equivalent clinical research experience can be demonstrated. Compensation: for the Senior Clinical Research Associate: Salary: $155,000-$175,000/year (USD) Benefits: Medical, Dental, Vision, 401(k), and applicable paid leave This job opens for applications on 10/30/26. Applications for this job will be accepted for at least 30 days from the posting date.