The Role
The Research Associate supports clinical trial operations by collecting and managing patient data, ensuring compliance with protocols, and assisting with recruitment and informed consent processes.
Summary Generated by Built In
City/State:
Bronx, New YorkGrant Funded:
YesDepartment:
Cancer Clinical Trials OfficeWork Shift:
DayWork Days:
MON-FRIScheduled Hours:
9 AM-5:30 PMScheduled Daily Hours:
7.5 HOURSPay Range:
$56,000.00-$70,000.00The Cancer Clinical Trials CRC I under direct supervision supports the research team in overall conduct of clinical trials using Good Clinical Practice. Mentored by an experienced Clinical Research Coordinator II or Sr. Clinical Research Coordinator, the CRC I is responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials.
Ensures timely collection of protocol related samples including shipment to outside entities as required. This individual obtains informed consent for non-interventional studies, participates and supports investigators in the informed consent process for interventional trials, collects, maintains and organizes study information including compilation, registration and submission of data, as required by the Sponsor. Attends clinic as needed to perform activities including, but not limited to: assist the research team with recruitment activities, administer questionnaires.
Essential Functions:
- Collects and records study data. Inputs all information into database
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
- Maintains source documents and subject files in accordance with hospital procedures.
- Ensures accurate and complete compilation of subject data through chart reviews.
- Upon assignment and under direct supervision, coordinates SFV, SIVs and monitor scheduling-- including remote access setup--for multiple studies.
- Secures, delivers and ships clinical specimens as required by the protocol.
Qualifications
Bachelors Degree Required
Masters Degree Preferred
ACRP (or SOCRA) certification preferred
Bachelor's degree in life science or public health, preferred
Medical Degree (or foreign equivalent), Preferred
Montefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law.Skills Required
- Bachelor's Degree
- Master's Degree
- ACRP or SOCRA certification
- Bachelor's degree in life science or public health
- Medical Degree or foreign equivalent
Am I A Good Fit?
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.
Success! Refresh the page to see how your skills align with this role.
The Company
What We Do
Montefiore is one of New York’s premier academic health systems, renowned for its leading medical school, groundbreaking research and technology, and highly specialized, coordinated care for diverse populations in the New York region, across the country and globally. Visit Montefiore.org to learn more.
