Clinical Research Coordinator

Join to apply for the Clinical Research Coordinator role at AMR Clinical
.

This role's base pay range is $24.00/hr - $31.00/hr
. Your actual compensation will depend on your skills and experience. The Clinical Research Coordinator will perform and manage tasks that are critical to clinical research studies, ensuring compliance with federal regulations, study protocol guidelines, and monitoring study participants while proactively identifying and resolving issues throughout the study.

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

Non-Exempt.

• Focus on compliance responsibilities, including protocol deviations, SAE reporting, and informed consent.
• 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.
• Understand and implement SOPs.
• Develop detailed knowledge of protocols and procedures for each study.
• Communicate effectively with study sponsors, CROs, monitors/CRAs, IRBs, laboratories, and clinical personnel.
• Serve as the study ambassador to advise team members on protocols and procedures.
• Establish and maintain patient rapport.
• Collect clinical data (vital signs, EKG recording, weight, height, etc.).
• Obtain and review medical records as required.
• Perform phlebotomy and specimen collection, processing, and storage.
• Transport clinical specimens to the laboratory.
• Educate subjects on diaries and oversee compliance with diary completion.
• Provide subjects with instructions on study procedures (diaries, restricted meds, study reminders, etc.).
• Conduct patient phone-call visits in accordance with protocol.
• Ensure documentation follows ALCOA standards and is timely.
• Complete required documentation and ensure it is signed and dated.
• Provide required information to CROs, IRBs, sponsors, FDA, and other agencies as needed.
• Manage study inventory and order supplies.
• Assist study monitors during onsite visits.
• Maintain familiarity with all ongoing clinical research studies.
• Attend investigator meetings as needed.
• Promote a team mentality by working flexible hours and completing tasks beyond core duties.
• Occasional weekend and/or overtime hours may be required.
• Other duties as assigned.

• 1 year of experience in clinical research.
• Completion of formal medical training, educational program, or healthcare experience.
• Strong medical terminology knowledge.
• 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‑pace evolving environment.
• Exceptional listening, written, and verbal communication skills.
• 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, or manipulate equipment and patients, requiring strength and 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.