Clinical Research Coordinator I

Position Summary

The Clinical Research Coordinator I conduct high quality clinical research following the highest ethical and regulatory standards of care.

Major Duties and Responsibilities

• Become familiar with the design of proposed and implemented studies.
• Review study protocols to evaluate factors such as sample collection processes, data management plans, and potential risks to subject patients.
• Communicate well with patients, medical personnel, research sponsors, and institutional review boards (IRBs).
• Assess eligibility of potential subjects through screening interviews, review of medical records, and discussion of patient status with physicians and nurses.
• Inform patients and caregivers of study designs, risks, and outcomes to be expected.
• Organize sites for study equipment and supplies.
• Contact industry representatives to ensure that the equipment and software specifications needed for successful study completion are available.
• Attend meetings required by research sponsors; some travel and overnight stays may be required.
• Enroll patients in clinical studies, ensuring that informed consent is obtained and documented in accordance with all applicable regulatory and ethical requirements at the federal, state, and local levels.
• Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
• Order the drugs and/or devices necessary for studies.
• Dispense medication and/or medical devices, calculate dosages, and provide instruction for patients as necessary.
• Comfortable handling lab specimens which may include blood, urine, vaginal fluids, joint aspirants, sputum or others.
• Competent in the processing, labeling specimen tubes, filling out requisitions, working with dry ice, storing and shipping lab specimens as required.
• Collect and maintain study data, which may be either electronic and/or printed, depending on the study.
• Obtain subject follow-up information and communicate with health care providers and subjects as necessary.
• Register protocol patients with appropriate statistical centers as required.
• Prepare and maintain records of study activities, including case report forms, drug dispensation records, and regulatory compliance.
• Prepare and maintain study-related protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
• Record adverse events and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
• Collaborate with investigators to prepare reports and presentations concerning clinical study procedures, results, and conclusions.
• Track enrollment status of subjects, document causes of dropout, and document efforts to contact subjects.
• Become familiar with relevant electronic medical records and HIPAA law.
• Monitor studies to ensure compliance with protocol design.
• Monitor studies to ensure compliance with federal, state and local regulations and TPMG's ethical policies.
• Prepare for and participate in audits conducted by study sponsors, federal agencies, and specifically designated review groups.
• Maintain contact with sponsors to schedule and coordinate site visits and answer questions about all issues with records or data
• Identify protocol problems, inform investigators of problems, and assist resolution of such problems
• Confer with health care professionals to determine the best recruitment practices for studies.
• Develop advertising and other informational materials to be used in subject recruitment.
• Meet with physician groups as needed.
• Participate in preparation and management of research budgets.
• Participate in the billing process for studies and oversee monetary disbursements.
• Participate in training and quality assurance programs.
• Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical study affairs and issues.
• Ability to work well independently and with a team.
• Ability to refocus attention easily after multiple interruptions.
• Ability to remain organized despite multiple paper charts being utilized at the same time.
• Using your own transportation to purchase dry ice for laboratory specimen shipments and taking the packages to USPS, UPS, and or FedEx for delivery as needed.
• Willing to perform work related tasks off-site when necessary.
• Willing and eager to learn new things.
• Other duties as assigned

Compensation starts at $52,243 per year, with the final annual salary determined by the candidate's relevant experience and qualifications.