Clinical Research Coordinator I-Eating and Weight Disorders Program at Mount Sinai
New York, NY 10029, USA -
Full Time


Start Date

Immediate

Expiry Date

20 Jun, 25

Salary

73530.0

Posted On

21 Mar, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Psychotherapy

Industry

Hospital/Health Care

Description

Qualifications

  • This position requires a candidate with a master’s degree, trained in psychotherapy as well as previous research and clinical experience. Education minimum is a master’s degree in a mental health field. A license is not required
Responsibilities

This position is for a full-time Clinical Research Coordinator I (CS02) in the Eating and Weight Disorders Program. This role primarily includes intervention delivery for research projects. Therapy is delivered to patient/parent pairs weekly for 6 months. It includes diagnostic interviews, therapy delivery, coding of therapy integrity from video recording, weekly supervision meetings, clinical notes, safety assessments, and communication as needed with participant physicians. Additionally, this role includes administrative tasks including recruitment, screening, retention, and data management. Recruitment and screening tasks include phone screening, semi-structured clinical interviews, running test meals and baseline assessments. Data management includes data entry, verification, and analysis for reporting. Paperwork for study development, regulatory approvals/renewals, and presentation/publication will be completed as needed.

Responsibilities

  • Collects and records study data. Inputs all information into database.
  • Obtains informed consent under minimal supervision of the investigator(s) 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, administering lifestyle questionnaires.
  • Assists in preparing grant applications, IRB/GCO for submission and filings.
  • 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.
  • Prepares for monitoring visits.
  • Performs other related duties.

Qualifications

  • This position requires a candidate with a master’s degree, trained in psychotherapy as well as previous research and clinical experience. Education minimum is a master’s degree in a mental health field. A license is not required.

Employer Description

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