Senior Clinical Research Associate

Clinical Research Associate / Senior CRA – Oncology (West Coast)

Location: Regional – West Coast (Remote with travel)

Company Overview:

Our client is a dynamic and growing US-based Contract Research Organization (CRO), specializing in clinical trials within the oncology space. Committed to delivering high-quality research solutions while fostering a collaborative and flexible work environment. As they expand operations, we are seeking an experienced Clinical Research Associate (CRA) / Senior CRA to join our clients team and support oncology trials across the West Coast.

Position Overview:

We are looking for a highly motivated and experienced CRA / Sr. CRA to monitor clinical trial sites across the West Coast. In this role, you will play a critical part in the success of oncology studies, ensuring that trial sites comply with regulatory requirements, protocol guidelines, and quality standards. The ideal candidate will have a solid background in clinical monitoring, with a focus on oncology, and at least 5-10 years of experience as a CRA.

Key Responsibilities:

• Perform site monitoring visits (initiation, interim, and close-out visits) across assigned West Coast locations.
• Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and protocol adherence at trial sites.
• Provide ongoing training and support to site staff.
• Manage study timelines, milestones, and deliverables, ensuring smooth site operations.
• Conduct site evaluations, assessments, and support investigator meetings.
• Ensure timely and accurate collection of clinical data and proper documentation.
• Identify and resolve issues or challenges at trial sites, including patient recruitment and retention.
• Collaborate with internal teams (clinical operations, regulatory, data management) to support trial success.
• Assist with the preparation of monitoring reports and presentations for sponsors and internal teams.
• Participate in regular project meetings and contribute to project strategy discussions.

Qualifications:

• 5-10 years of experience as a CRA, with at least 3 years in oncology clinical trials.
• Strong knowledge of oncology trial processes, protocols, and related regulatory requirements (FDA, ICH-GCP).
• Previous experience with monitoring Phase I-III oncology studies is a plus.
• Ability to work independently and manage multiple tasks and timelines.
• Excellent communication, organizational, and interpersonal skills.
• Strong problem-solving skills and attention to detail.
• Ability to travel regionally within the West Coast (up to 50-75% travel).
• A degree in life sciences, nursing, or related field is preferred.
• CRA certification (CCRC or ACRP) is a plus.

How to Apply:

Please submit your resume and a brief cover letter highlighting your relevant experience to [email protected]