Research Associate

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

Job summary

The Montefiore Hudson Valley Collaborative is seeking a Research Associate to support the Cancer Clinical Trials Office's solid tumor program. Under supervision, you will collect and manage patient data and assist with consent and sample handling in interventional and non-interventional studies.

You will participate in screening, data entry into our databases, and coordinating scheduling and shipments, ensuring source documents are complete and compliant with Good Clinical Practice.

Qualifications

• Bachelor's degree in life science or public health required.
• Master's degree preferred; related advanced degrees welcomed.
• ACRP or SOCRA certification preferred.

Responsibilities

• Collects and records study data; inputs information into database.
• Assists in activities related to clinical research studies, including screening participants.
• Maintains source documents and subject files per hospital procedures.
• Coordinates scheduling and monitoring visits, including remote access setup.
• Secures, delivers and ships clinical specimens as required by protocol.
• Supports informed consent processes for interventional and non-interventional trials.

Skills

Data collection

Good Clinical Practice

Informed consent

Clinical trial coordination

Education

Bachelor's degree in life science or public health

Master's degree preferred

Medical Degree (or foreign equivalent), preferred

Tools

ACRP/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