Clinical Research Coordinator (CRC)

COMPANY OVERVIEW

United Theranostics is redefining the clinical practice of molecular imaging and radiopharmaceutical therapy from available to meaningful accessibility. Our network of nuclear medicine facilities specializes in personalized cancer treatment, combining advanced diagnostics with targeted radionuclide therapies. We bring the latest in precision medicine to patients in their local communities.

SUMMARY

The Clinical Research Coordinator (CRC) is in charge of daily operations of clinical trials. The research coordinator will screen, enroll, and follow study subjects for clinical trials, ensuring protocol compliance and close monitoring throughout the subjects participation in the study. The position is based at our Princeton, New Jersey clinic and requires daily onsite attendance.

RESPONSIBILITIES

Conducting Clinical Trials

• Review the protocol, study design, inclusion/exclusion criteria, schedule of events, and the informed consent form to ensure understanding.
• Develop and implement strategies for subject recruitment and ongoing communications with physicians, research staff, and office staff.
• Prepare study charts, binders, and supplies for upcoming subject visit.
• Ensure maintenance and calibration of study equipment.
• Ensure that all study supplies are stocked and check expiration dates.

Enrolling Study Subjects and Conducting Follow Up Visits/Procedures

• Review, verify, and record relevant documentation in the subjects medical record needed to confirm study eligibility.
• Ensure the current approved informed consent is signed before subjects are screened and enrolled.
• Perform delegated protocol specific tasks as assigned
• Ensure that the randomization procedures are followed and documented per protocol guidelines.
• Document all study procedures, adverse events, and changes to concomitant medications per protocol throughout the duration of the subjects participation in the trial.
• Communicate with PI and nuclear technologists to ensure timely and accurate study drug administration, scans and PK’s when applicable
• Report any Serious Adverse Events and/or Protocol Deviations to the PI and Central Research Office as soon as possible upon knowledge of the event.
• Maintain accurate and complete documentation, including but not limited to signed informed consent forms, source documentation, accountability logs, subject logs, and study-related communications.

Conduct On-Site and Remote Monitoring Visits

• Assist the study monitor with on-site or remote monitoring visits.
• Resolve any action items/findings in a timely manner after each monitoring visit is completed.

QUALIFICATIONS

• Minimum High School Diploma or GED required.
• Minimum of 7+ years of clinical research experience.
• Maintained ACRP or SOCRA certification is preferred but not required

Job Type: Full-time

Pay: $70,000.00 - $90,000.00 per year

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Application Question(s):

• What is your desired salary range?

Ability to Commute:

• Princeton, NJ 08540 (Required)

Work Location: In person