Senior Clinical Research Associate

Responsibilities

• 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

• 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.

Pay

Salary: $155,000-$175,000/year (USD)

Benefits

• Medical
• Dental
• Vision
• 401(k)
• applicable paid leave