Sr. CRA, Oncology, IQVIA Biotech (Oncology)

Location: Durham, North Carolina, United States of America

Salary: $105,100–$197,500 annualized base pay

Company

IQVIA Biotech is a full-service contract research organization serving biotechnology sponsors with clinical research, healthcare intelligence, and commercialization support.

What you will do

• Independently manage and monitor clinical trial sites across multiple phases of clinical research.
• Conduct site qualification, initiation, routine monitoring, and closeout visits.
• Support patient recruitment and retention and provide protocol and study-related training.
• Review source documentation, track study milestones, resolve data queries, and oversee site performance.
• Maintain regulatory and essential documents and prepare accurate monitoring reports.
• Collaborate with cross-functional study teams and mentor junior clinical research associates.

Requirements

• Bachelor’s degree in a scientific, healthcare, or related discipline, or an equivalent combination of education and experience.
• Minimum of 4 years of on-site clinical monitoring experience.
• Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes.
• Experience conducting monitoring visits across multiple clinical research phases.
• Excellent organizational, communication, and problem-solving skills with the ability to manage multiple priorities.
• Proficiency with Microsoft Office applications and clinical trial systems.

Nice to have

• Strong therapeutic area knowledge and protocol management experience.
• Experience building productive relationships with investigative sites, sponsors, and internal study teams.
• Experience mentoring or supporting junior clinical research professionals.

Culture & Benefits

• Full-time employment within a global clinical research organization.
• Health and welfare benefits may be provided.
• Incentive plans, bonuses, or other compensation may be offered depending on the position.
• Equal opportunity employment is provided.