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Clinical Research Coordinator(Data)
Actalent
An engineering and sciences services and talent solutions firm connecting specialized experts with industry projects.
Coordinating initiation and activation of clinical trial protocols, focusing on data entry and query resolution for oncology trials.
23d ago
$25 - $35
Junior (1-3 years)
Contractor
Bronx, NY
Onsite
Company Size
5,000 Employees
Service Specialisms
Technical consultation
Performance analysis
Physical development
Injury prevention and recuperation
Sports psychology
360° Marketing
Consultancy with clubs and sporting entities
Legal services
Sector Specialisms
Utilities
Power
Automotive
Food and Beverage
Consumer Products
Industrial Goods
Manufacturing
Mechanical Engineering
Role
What you would be doing
develop study tools
grade adverse events
coordinate trials
complete sae forms
maintain research records
provide reports
Develop study tools using Oncore®, Excel®, and Word.
Assist with grading adverse events using NCI common toxicity criteria or protocol-specific grading scales.
Coordinate the initiation and activation of new clinical trial protocols.
Complete Serious/Unexpected Adverse Event forms as required.
Prepare study tools, including study binders, medication diaries, eligibility checklists, and flow sheets.
Review patients’ charts and medical history in collaboration with the RNC and/or physician.
Maintain research records for all patients enrolled in studies.
Ensure informed consent forms are obtained, signed, and recorded.
Provide regular reports to tumor study group members and Principal Investigators.
Serve as a liaison with study sponsors, schedule monitoring visits and conference calls, and respond to sponsors’ queries.
What you bring
clinical research
oncology
ocn
iata
supervisory
medication
1-2 years of clinical research coordinator experience, primarily focused on data entry and query resolution for oncology trials.
Experience in screening, enrolling, and consenting patients into research studies based on study protocols.
Oncology Certified Nurse (OCN) or related certification.
IATA certification.
3-5 years of clinical research experience, with a minimum of 2 years considered.
Experience in medication administration to patients.
Prior supervisory experience and experience in onboarding/training new clinical research coordinators.
Benefits
Health Spending Account (HSA)
Medical, dental & vision
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Critical Illness, Accident, and Hospital
Short and long-term disability
Transportation benefits
Employee Assistance Program
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
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