Job description

Pain Management Practice looking for Clinical Research Coordinator to manage clinical trials, including some regulatory and budget requirements, recruitment, and coordination of tests/visits for patients.

GENERAL STUDY MANAGEMENT Responsibilities Include:

Reviewing research protocols

Assisting Principal Investigators in study start up and submitting studies to appropriate offices

Interacting with the regulatory team to maintain regulatory documentation and administrative files for each protocol

Maintains procedures necessary for timely and complete data management and complies with required supervision tools such as work logs and regular meetings

Coordinates study enrollment, protocol treatment, and follow-up care for patients participating in clinical trials in conjunction with the PI

Recruits and confirms that each patient meets eligibility criteria specified for protocols and enrollment into clinical trials

Communicating with various departments, physicians, labs, outside hospitals, and all members of the clinical team to ensure accuracy, timely retrieval of data, and confirm the appropriateness and timeliness of tests

Collecting follow-up data on patients' post-treatment as required by the protocol and submit monthly reports to the clinical protocol office, tracking patient enrollment and accounts/payments for sponsored protocols

Completes timely research billing review

Maintains and updates sponsor-related, and practice related databases/logs

Handling data management requirements for each patient enrolled

Coordinator performs other related duties and participates in special projects as assigned

Job Type: Full-time

Pay: $50,000.00 - $60,000.00 per year

Benefits:

• Paid time off

Schedule:

• 8 hour shift
• Monday to Friday

Ability to commute/relocate:

• New York, NY 10022: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Clinical Trials Coordinator: 2 years (Required)

Work Location: One location

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