This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Clinical Research Associate (CRA) in United States.
This role is central to the successful execution of Phase I–IV clinical trials, ensuring high-quality data collection, regulatory compliance, and effective site management across multiple investigative locations. You will act as the primary point of contact for assigned clinical sites, supporting study start-up, ongoing monitoring, and close-out activities in line with global clinical research standards. The position requires frequent travel and close collaboration with site staff and internal clinical teams to ensure patient safety and protocol adherence. You will play a key role in maintaining data integrity and driving timely delivery of trial milestones in a fast-paced, regulated environment. This is a highly field-based role offering strong exposure to global clinical operations and cross-functional collaboration. The position is remote within the United States, with proximity to a major airport required.
Accountabilities:- Serve as the primary site manager and main liaison between clinical trial sites and internal study teams, ensuring effective communication and collaboration.
- Conduct site initiation, monitoring visits (onsite and remote), and close-out activities in accordance with study protocols and regulatory requirements.
- Ensure sites are properly trained on study procedures, amendments, and compliance expectations, maintaining thorough documentation.
- Monitor study conduct to ensure adherence to ICH-GCP, FDA/EMA regulations, and internal SOPs, safeguarding patient safety and data integrity.
- Track study progress, manage timelines, and ensure timely, accurate, and high-quality data delivery from assigned sites.
- Identify, resolve, and escalate site-related issues while supporting efficient query resolution and data cleaning processes.
- Collaborate with cross-functional teams including clinical project managers, medical experts, and site partners to support overall study execution.
- Maintain up-to-date documentation across clinical trial systems and ensure accurate reporting of monitoring activities.
Requirements:
- Bachelor’s degree in Life Sciences, Healthcare, or a related scientific field.
- Minimum of 3 years of experience in clinical site monitoring or clinical research associate roles.
- Strong knowledge of clinical trial processes, drug development lifecycle, and regulatory frameworks (ICH-GCP, FDA, EMA).
- Proven ability to manage multiple studies, prioritize tasks, and operate effectively in a fast-paced environment.
- Strong site management, negotiation, and problem-solving skills with attention to detail.
- Excellent communication skills, both written and verbal, with the ability to engage diverse stakeholders.
- Ability to travel up to approximately 80% domestically and internationally as required.
- Preferred: experience in oncology, radioligand therapy (RLT), or CAR-T programs.
Benefits:
- Competitive salary range between $108,500 and $201,500 annually.
- Performance-based cash incentives and eligibility for equity awards depending on role level.
- Comprehensive health, life, and disability insurance coverage.
- 401(k) retirement plan with company contribution and matching.
- Generous paid time off including vacation, holidays, personal days, and additional leave options.
- Opportunities for professional growth within global clinical research and pharmaceutical development.
- Exposure to advanced clinical programs and cutting-edge therapeutic areas.
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!
Why Apply Through Jobgether?
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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