Clinical Research Coordinator- Div Gen Int Medicine

Mount Sinai; United States; On-site; USD 55,000 - 75,000; Full time

Job summary

Mount Sinai is seeking an entry-level Clinical Research Coordinator to assist in conducting clinical studies under the supervision of the Principal Investigator or senior staff. Responsibilities include obtaining informed consent, screening participants, registering patients, and assisting with data collection, analysis, and regulatory documentation.

The role supports preparation for regulatory site visits and ensures accurate, confidential data management in line with Mount Sinai policies.

Qualifications

• Bachelor's degree preferred or combination of relevant research experience and education.
• 0-2 years of research/human subjects experience.

Responsibilities

• Conducts routine and standardized human subjects research under supervision of the PI or senior staff.
• Obtain informed consent, screen participants for eligibility, register patients with sponsoring agencies, administer questionnaires and respond to calls.
• Assist in collection, analysis and review of experimental data for publication.

Skills

Informed consent

Interview techniques

Data collection

Education

Bachelor's degree in science or related field

Job description

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects, maintains and organizes study information. Assists in the preparation and submission of grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office).

• Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Principal Investigator or senior clinical research staff.
• Assists in the activities related to clinical research including, but not limited to: obtaining informed consent, screening participants for eligibility, registering patients with sponsoring agencies, administering questionnaires and answering telephone calls.
• Assists in the collection, analysis and review of experimental data for publication and presentation.
• Maintains source documents and subject files in accordance with Mount Sinai policies and procedures. Ensures accurate, confidential and complete compilation of data.
• May secure and ship clinical specimens as required by the protocol.
• May assist in the preparation for regulatory agency site visits.
• Performs other related duties.

• Bachelors degree in science or related field preferred or a combination of relevant research experience and education
• 0-2 years of research/human subjects experience