Clinical Research Associate
Trenton, NJFull-time
Behavioral Health Market Context
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Benefits
In addition to your competitive salary, ICON offers a range of additional benefitsOur benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your familyVarious annual leave entitlementsA range of health insurance offerings to suit you and your family's needsCompetitive retirement planning offerings to maximize savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among othersActual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill levelYou may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance7 more items(s)
Qualifications
- •A graduate with a Bachelor's degree in Life Sciences or equivalent, or a qualified RN
- •Eligible to work in United States without visa sponsorship
- •A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry
- •Experienced Oncology Hematology area required
- •Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
- •A clear communicator, problem-solver, and collaborative team player
- •Willing and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in New York City, near major HUB airports to support efficient regional travel
- •4 more items(s)
Responsibilities
- •Serve as the primary point of contact between investigational sites and the sponsor
- •Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
- •Ensure site compliance with ICH-GCP, SOPs, and regulations
- •Maintain up-to-date documentation in CTMS and eTMF systems
- •Support and track site staff training and maintain compliance records
- •Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
- •Support subject recruitment and retention efforts at the site level
- •Oversee drug accountability and ensure proper storage, return, or destruction
- •Resolve data queries and drive timely, high-quality data entry
- •Document site progress and escalate risks or issues to the clinical team
- •Assist in tracking site budgets and ensuring timely site payments (as applicable)
- •Collaborate with cross-functional partners including CTAs, LTMs, and CTMs
- •9 more items(s)
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