Clinical Research Coordinator I: Data, Consent & Grants

Mount Sinai; New York (NY); Sur place; USD 59 000 - 74 000; Plein temps

Résumé du poste

Mount Sinai Health System in New York is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and maintain study information. The role involves data entry, organization of documents, and assisting with IRB submissions and grant materials.

You will assist with participant screening, scheduling, and coordinating dispatch of samples, while ensuring compliance with hospital procedures and ethical standards.

Qualifications

• Bachelors or Masters degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Responsabilités

• 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.

Connaissances

Informed consent

Data collection

Clinical research

Formation

Bachelor's or Master's in Science

Description du poste

Mount Sinai Health System in New York is seeking a Clinical Research Coordinator to support daily activities of clinical research studies, obtain informed consent, and maintain study information. The role involves data entry, organization of documents, and assisting with IRB submissions and grant materials.

You will assist with participant screening, scheduling, and coordinating dispatch of samples, while ensuring compliance with hospital procedures and ethical standards.