Senior Clinical Research Associate - Oncology
$110,520–$138,150 year
On-siteNew York City, New York, United States or New Jersey, United States
Job Summary
Serve as the primary point of contact between investigational sites and the sponsor, conducting all site visits including selection, initiation, routine monitoring, and close-out. Ensure site compliance with ICH-GCP, SOPs, and regulations while maintaining up-to-date documentation in CTMS and eTMF systems. Monitor patient safety through timely AE/SAE/PQC reporting, support subject recruitment, and oversee drug accountability. Resolve data queries, document site progress, escalate risks, and assist in tracking site budgets. This role requires 3+ years of on-site monitoring experience in oncology, hematology, or prostate cancer, with up to 50% travel across the northeast region. Salary range is $110,520.00-$138,150.00.
Required Qualifications
- Bachelor's degree in Life Sciences or equivalent
- Qualified RN
- Eligible to work in United States without visa sponsorship
- 3+ years of on-site monitoring experience in the pharmaceutical or CRO industry
- Experience across multiple therapeutic areas, ideally including Oncology (Prostate Cancer, and Lung Cancer) and Hematology
- Proficiency in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
- Clear communicator, problem-solver, and collaborative team player
- Willing and able to travel up to 50% for on-site monitoring visits across northeast region
- Preference given to candidates residing in NJ / NY near major HUB airports to support efficient regional travel
- Legal right to work in the country where the role is based
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