Clinical Research Associate II - Oncology

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

As a Clinical Research Associate II, you’ll play a critical role in ensuring clinical studies are conducted to the highest standards of quality, compliance, and patient safety. Your work will directly support the successful delivery of clinical research by partnering with investigative sites and study teams throughout the study lifecycle. In this role, you’ll take ownership of site qualification, initiation, monitoring, management, and close‑out activities while helping ensure accurate, timely, and reliable study data.

You’ll serve as a trusted resource for site personnel, providing guidance, training, and support to promote protocol adherence and regulatory compliance. Working across multiple stakeholders, you’ll contribute to the success of clinical trials by driving data quality, supporting safety reporting, and maintaining strong site relationships that help advance important research programs.

This is a home‑based Clinical Research Associate role supporting sites across the United States. Candidates must reside within the territory to effectively support site visits and study activities. You will collaborate with sites, sponsors, and global study teams while traveling to investigative sites approximately 8-10 days per month. To best support our sites, we’re seeking candidates who are based in the United States.

Travel will primarily be regional, with occasional travel to support sites in other locations as needed.

• Conduct site qualification, initiation, monitoring, and close‑out visits in accordance with study protocols, GCP requirements, and applicable regulations.
• Evaluate site feasibility and readiness to support successful study execution.
• Review and maintain essential regulatory, ethics, and study documentation to ensure compliance and inspection readiness.
• Train and support site personnel on protocol requirements, study procedures, and data quality expectations.
• Verify source documentation and review study data to ensure accuracy, completeness, and protection of patient safety.
• Partner with sites to resolve data queries, maintain investigator files, and support timely study deliverables.
• Monitor investigational product accountability, including receipt, storage, return, or destruction activities.
• Prepare detailed visit reports and provide updates for inclusion in the Trial Master File.
• Collaborate with study teams and contribute expertise to protocol, CRF, and monitoring plan development when requested.

• Bachelor’s…