Clinical Research Coordinator I - Urology

Mount Sinai; United States; On-site; USD 60,000 - 75,000; Full time

Job summary

Mount Sinai in the United States seeks a Clinical Research Coordinator to support daily activities of clinical research studies within the urology program. You will collect data, obtain consent, screen participants, and assist with regulatory submissions and grant-related tasks.

The role involves maintaining study documentation, handling specimens, and preparing for monitoring visits, with an emphasis on accuracy and compliance.

Qualifications

• Bachelor's or Master's degree in Science or closely related field.
• No experience required; one year of research experience preferred.

Responsibilities

• Collect and record study data and input into database.
• Obtain informed consent and educate participants on study requirements.
• Screen participants for eligibility and register subjects with sponsoring agency.
• Administer lifestyle questionnaires and assist in related study activities.
• Prepare grant applications and IRB/GCO submissions and filings.
• Maintain source documents and subject files following hospital procedures.
• Secure, deliver and ship clinical specimens as required by the protocol.
• Prepare for monitoring visits and perform other related duties.

Skills

Data collection

Informed consent

Participant screening

IRB knowledge

Education

Bachelor's or Master's in Science

Job description

The Milton and Carroll Petrie Department of Urology has long been a leader in clinical practice, education, and research. Faculty in our Department, which is housed within the Icahn School of Medicine at Mount Sinai, perform complex procedures using robotics, laparoscopy, and endoscopy, all as a part of our minimally invasive urologic surgery program. We remain equally committed to engaging in breakthrough research while training the next generation of leaders in the field.

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).

• 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.

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