Clinical Trials Research Associate I

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

Job summary

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.

Responsibilities

• 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.

Education

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)

Job description

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.