Clinical Research Coordinator I-Depression and Anxiety Center for Discovery and Treatment (DAC)

Mount Sinai Health System • New York, NY

19h

About The Position

Clinical Research Coordinators at the Depression and Anxiety Center for Discovery and Treatment (DAC) are responsible for administrative, academic and clinical tasks including: running experimental procedures, entering and analyzing data, conducting phone screens on potential subjects, study development paperwork, presentation/publication preparation. Under minimal supervision, coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (e.g., for Institutional Review Board, Grants and Contracts Office). Potential opportunities available to successful DAC coordinators include: publication in major medical journals; networking among distinguished individuals within and outside the medical/psychology fields; exposure to wide spectrum of psychiatric disorders and treatments thereof. This position will require an individual who understands basic principles of scientific investigation and clinical trials and who is capable of in-depth understanding of the project's study protocol. Thus, the incumbent must possess excellent scientific, organizational, and interpersonal skills; the incumbent must also have a background in psychology to manage the technical aspects of the study.

Requirements

• Bachelors or Masters degree in Science or closely related field.
• No experience required.
• Excellent verbal, written & interpersonal skills.
• Knowledge of standard concepts, practices and procedures in directly related field.
• Exceptional attention to detail and accuracy

Nice To Haves

• One year of research experience preferred.

Responsibilities

• Coordinates the clinical assessments and study visits of participants, including but not limited to screening and evaluation of participants.
• Ensures accurate and complete compilation of subject data, which may include chart reviews.
• Obtains informed consent under supervision of the Principal Investigator, Research Manager, or Clinical Trials Manager for human subjects research.
• Assists in the analysis, including cleaning and organizing, of moderately complex clinical research data.
• Prepares and ensures IRB and/or GCO documents are submitted.
• Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials.
• Performs other related duties.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level