Urology Clinical Research Coordinator I — Frontline Trials

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

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.