Senior Clinical Research Associate (CRA)

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.
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