Clinical Research Coordinator I – Cancer Trials

Mount Sinai

United States

On-site

USD 52,000 - 76,000

Full time

4 days ago
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Job summary

The Tisch Cancer Center at Mount Sinai Hospital is seeking a Clinical Research Coordinator I to support cancer studies. Responsibilities include data collection, specimen handling, obtaining informed consent, and maintaining study information in databases.

Under supervision, you will screen participants, record data, manage documents, and prepare for monitoring visits. A Bachelor’s or Master’s degree in Science or a related field is required; no experience is required, though one year of

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 activities related to clinical research studies including 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; ensures 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.

Skills

Data collection
Informed consent
Participant education
Study coordination
Documentation

Education

Bachelor's or Master's in Science or related field

Job description

The Tisch Cancer Center at Mount Sinai Hospital is seeking a Clinical Research Coordinator I to support cancer studies. Responsibilities include data collection, specimen handling, obtaining informed consent, and maintaining study information in databases.

Under supervision, you will screen participants, record data, manage documents, and prepare for monitoring visits. A Bachelor’s or Master’s degree in Science or a related field is required; no experience is required, though one year of

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