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 invites applications for a Clinical Research Coordinator to support daily activities of clinical studies. You will collect and organize study information, obtain informed consent, and help prepare grant applications and IRB submissions.

Responsibilities include data entry, participant screening, subject registration with sponsors, handling specimens, and preparing for monitoring visits. A BS or MS in science is required or preferred; no prior experience is necessary.

Qualifications

• Bachelor's or Master's 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 activities related to clinical research studies including 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.

Formation

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

Description du poste

Mount Sinai invites applications for a Clinical Research Coordinator to support daily activities of clinical studies. You will collect and organize study information, obtain informed consent, and help prepare grant applications and IRB submissions.

Responsibilities include data entry, participant screening, subject registration with sponsors, handling specimens, and preparing for monitoring visits. A BS or MS in science is required or preferred; no prior experience is necessary.