Senior Clinical Research Associate [Remote]

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.

Accountabilities:

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

Requirements:

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

Benefits:

• 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

How Jobgether works:

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.

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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.