Clinical Research Coordinator

This range is provided by AMR Clinical. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$29.00/hr - $31.00/hr

The Clinical Research Coordinator will perform and manage tasks that are critical to clinical research studies. The Clinical Research Coordinator must ensure compliance with federal regulations, study protocol guidelines, as well as monitor study participants, and take a proactive approach to identify issues on an ongoing basis throughout the clinical research study.

• United We Achieve
• Celebrate Diverse Perspectives
• Do the Right Thing
• Adapt and Persevere

The Clinical Research Coordinator reports to the Site Manager/Team Lead.

Classification:
Non-Exempt

• Focus on compliance responsibilities, including protocol deviations, SAE reporting, and informed consent procedures.
• Coordinate clinical trials per FDA requirements and GCP Guidelines per sponsor protocols.
• Manage and document Adverse Event and Serious Adverse Event reporting in compliance with FDA, IRB, and sponsor requirements, ensuring timely follow-up and resolution.
• Establish understanding of SOPs and implement them.
• Gain understanding of the pharmaceutical drug per clinical trial.
• Develop detailed knowledge of protocol and procedures per clinical research study.
• Communicate effectively with study sponsors, CROs, monitors/CRA’s, IRBs, laboratories, and clinical personnel.
• Act as the study ambassador on assigned studies to advise team members on protocols and procedures.
• Establish and maintain patient rapport.
• Perform clinical data collection (vital signs, EKG recording, weight, height, etc.).
• Obtain medical records and review as required.
• Phlebotomy.
• Specimen collection, processing, and storage.
• Transport clinical specimens to the laboratory.
• Educate subjects on diaries and oversee compliance with diary completion.
• Provide subjects instructions per study (diaries, restricted meds, study reminders, etc.).
• Responsible for completing patient phone call visits in accordance to the standard protocol period.
• Ensure documentation follows ALCOA standards and is completed in a timely manner.
• Ensure all necessary documents are completed, signed and dated.
• Provide required information to CRO, IRB, sponsoring organization, FDA, and/or other agency as required.
• Manage study inventory and order supplies as needed.
• Prepare and assist study monitors during onsite visits.
• Maintain familiarity with all ongoing clinical research studies.
• Travel to investigator meetings as needed.
• Promote team mentality by working flexible hours, completing tasks outside everyday duties.
• Position may require occasional weekend and/or overtime hours.
• Other duties as assigned.

• 1 year of experience in clinical research.
• Completion of formal medical training, educational program, or healthcare experience.
• Strong medical terminology.
• Ability to perform clinical, laboratory, and diagnostic tests (vital signs, height, weight, temperature, etc.).
• Ability to work independently and lead study-related tasks.
• Ability to multi-task in a high‑paced evolving environment.
• Exceptional listening, written, and verbal communication skills.
• Demonstrate proficiency in office equipment and software programs.
• Excellent organizational and task management skills.
• Ability to be ambulatory most of the workday.
• Ability to lift/transfer/push/manipulate equipment and patients, requiring strength, gross motor and fine motor coordination.

AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non‑merit factor.

• This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job‑related tasks other than those stated in this description.