Clinical Research Coordinator I: Cancer Trials & Data Support

Mount Sinai; New York (NY); On-site; USD 59,000 - 74,000; Full time

Job summary

A Clinical Research Coordinator I position is available at the Tisch Cancer Center, part of the Mount Sinai Health System in New York. Duties include data collection, specimen handling, obtaining informed consent, and maintaining study information in accordance with hospital procedures.

The role supports monitor visits, coordinating clinical trials, and communicating with sponsors under supervision. A Bachelor's or Master's in science is required or preferred; no experience is required, with one

Qualifications

• Bachelor's or Master's degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Responsibilities

• Collects and records study data; inputs all information into database.
• Under direct supervision of the Principal Investigator(s), obtains informed consent and educates participants regarding study requirements.
• 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, and administering lifestyle questionnaires.
• Maintains source documents and subject files in accordance with hospital procedures; helps to ensure accurate and complete compilation of subject data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Responsible for organizing and preparing for monitoring visits.
• Assists with coordination and management of clinical trials including communication with Sponsors.
• Performs other related duties as assigned.

Education

Bachelor's or Master’s degree in Science or closely related field

Job description

A Clinical Research Coordinator I position is available at the Tisch Cancer Center, part of the Mount Sinai Health System in New York. Duties include data collection, specimen handling, obtaining informed consent, and maintaining study information in accordance with hospital procedures.

The role supports monitor visits, coordinating clinical trials, and communicating with sponsors under supervision. A Bachelor's or Master's in science is required or preferred; no experience is required, with one