Research Associate

Montefiore Medical Center; New York (NY); Sur place; USD 56 000 - 70 000; Plein temps

Résumé du poste

Montefiore Medical Center in Bronx, NY is hiring a Clinical Trials Coordinator I to support cancer studies in the solid tumors program. The role involves data collection, entry into databases, and assisting in recruitment and consent for interventional and non-interventional trials.

Under supervision, you will coordinate visits, SFVs/SIVs, and monitor scheduling across multiple studies, including remote access where required, and handle specimen shipments following protocol guidelines.

Qualifications

• Bachelor's degree in life science or public health required.
• Masters degree preferred.
• ACRP or SOCRA certification preferred.
• Bachelor's/Bachelor's in life science or public health preferred.
• Medical degree (or foreign equivalent) preferred.

Responsabilités

• Collects and records study data; inputs into database.
• Assists in protocol-related activities: screening, registering subjects, administering questionnaires.
• Maintains source documents and subject files per hospital procedures.
• Coordinates SFVs, SIVs and monitor scheduling, including remote access setup, for multiple studies.
• Secures, delivers and ships clinical specimens as required by the protocol.

Formation

Bachelor's Degree (Life Science or Public Health)

Master's Degree

ACRP/SOCRA Certification

Medical Degree or Foreign Equivalent

Bachelor's Degree (Life Science or Public Health)

Description du poste

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-$70,000.00

The 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.