Research Associate

Montefiore New Rochelle; New York (NY); On-site; USD 56,000 - 70,000; Full time

Job summary

Montefiore New Rochelle is seeking a Research Associate to support clinical trials in the Cancer Clinical Trials Office. This role involves data collection, data management, and coordinating activities under supervision to ensure GCP-compliant conduct and timely data submission.

You will assist in participant recruitment, consent processes for interventional and non-interventional studies, and help maintain study documentation and specimen handling per protocol.

Qualifications

• Bachelor's degree in life science or public health required.
• Master's degree preferred for advanced responsibilities.
• ACRP or SOCRA certification preferred.

Responsibilities

• Collects and records study data and inputs information into the database.
• Assists in trial activities: calling participants, screening eligibility, registering subjects with sponsors, and administering lifestyle questionnaires.
• Maintains source documents and subject files per hospital procedures.
• Ensures data accuracy through chart reviews and timely data compilation.
• Coordinates SFVs and SIVs and monitors scheduling, including remote access where needed.
• Secures and ships clinical specimens as required by the protocol.

Education

Bachelor's Degree

Master's Degree

ACRP or SOCRA certification

Job description

Research Associate### Research AssociateApply: 1695 Eastchester Road: Full time: Posted Today: JR235177**City/State:**Bronx, New York**Grant Funded:**Yes**Department:**Cancer Clinical Trials Office - Operations-Solid Tumors**Work Shift:**Day**Work Days:**MON-FRI**Scheduled Hours:**9 AM-5:30 PM**Scheduled Daily Hours:**7.5 HOURS**Pay 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 RequiredMasters Degree PreferredACRP (or SOCRA) certification preferred Bachelor's degree in life science or public health, preferredMedical Degree (or foreign equivalent), Preferred