Senior Clinical Research Associate in United States at Jobgether

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Research Associate based in the United States.

You will play a key role in advancing clinical trials by ensuring high-quality execution at the site level across Phase I–IV studies.
The role focuses on building strong, trusted relationships with investigational sites to drive performance and patient-centered outcomes.
You will conduct both on-site and remote monitoring activities to ensure compliance with ICH/GCP guidelines and study protocols.
This position requires proactive risk identification, issue resolution, and consistent oversight of data quality and site readiness.
You will collaborate closely with cross-functional clinical teams to support timely study delivery and operational excellence.
Assigned to complex studies, you may act as a subject matter expert and contribute to inspection readiness and process improvements.
This is a highly dynamic, field-based role with extensive travel and strong exposure to global clinical research operations.

In this role, you will be responsible for leading site-level clinical trial execution and ensuring adherence to quality and regulatory standards.

• Serve as the primary point of contact for assigned investigational sites throughout the study lifecycle
• Conduct site initiation, monitoring visits (on-site and remote), and ongoing site support activities
• Ensure compliance with ICH/GCP, protocol requirements, SOPs, and applicable regulatory standards
• Monitor patient safety, data integrity, and timely resolution of data queries and issues
• Identify, assess, and escalate risks while implementing appropriate corrective and preventive actions
• Support inspection and audit readiness activities and ensure timely documentation updates
• Collaborate with cross-functional teams to optimize study timelines and operational efficiency

The ideal candidate brings strong clinical research monitoring experience and the ability to manage complex, multi-site studies independently.

• Bachelor’s degree in life sciences, healthcare, or a related scientific field
• Minimum of 3+ years of clinical site monitoring experience in clinical research
• Strong knowledge of clinical trial processes, drug development, and ICH/GCP guidelines
• Experience managing multiple priorities in a fast-paced, regulated environment
• Excellent communication, problem-solving, and relationship management skills
• High attention to detail with strong organizational and documentation abilities
• Fluency in written and spoken English
• Willingness and ability to travel extensively (up to 80% nationally)
• Experience in oncology or advanced therapies (e.g., radioligand or CAR-T) is a plus

• Competitive annual salary range: $108,500 – $201,500 (based on experience and skills)
• Performance-based cash incentives and eligibility for annual equity awards
• Comprehensive health, life, and disability insurance coverage
• 401(k) retirement plan with company contribution and matching
• Generous paid time off including vacation, personal days, holidays, and leave options
• Opportunities for professional growth in global clinical research environments
• Flexible, remote-based role with nationwide travel opportunities