Clinical Research Coordinator: Data, Screening & Protocols

Urology Centers of Alabama; Homewood (IL); On-site; USD 52,000 - 76,000; Full time

Job summary

Urology Centers of Alabama seeks a Research Coordinator to manage screening, data collection, and protocol adherence across clinical studies. You will coordinate patient visits, tests, and sample handling while ensuring ICH/GCP, CFR, IATA, and HIPAA compliance within the study framework.

The role requires engagement with physicians and staff, attention to documentation accuracy, and timely communication with sponsors and monitors. Day shift, full-time on-site in Homewood, IL.

Qualifications

• Must be current in ICH/GCP training.
• Must have previous clinical lab experience, including phlebotomy.
• Must be able to perform ECGs and document vital signs.
• Proficient with office equipment: PC, Windows, MSOffice, EMR, multi-line phones, copier, fax.
• Must have a Basic Life Support (BLS) CPR certification, up to date.
• Must travel to continuing education seminars or conventions as needed.
• Must demonstrate excellent interpersonal communication across diverse groups.
• Must work independently or in a team in a fast-paced environment.
• Must maintain confidentiality including HIPAA and UCA guidelines.

Responsibilities

• Review and implement protocols for screening, collecting, and compiling patient data.
• Attend Investigator Meetings and seminars; may require overnight travel.
• Recruit and pre-screen patients for actively enrolling protocols.
• Educate physicians and nursing staff about active protocols.
• Perform Screening Visits and obtain initial written consent.
• Coordinate all patient visits, tests and procedures per protocol requirements.
• Perform ECGs and document vital signs.
• Collect, process and ship specimens per protocol and IATA.
• Document data at each visit on source documents and CRF.
• Maintain communication with patients and physicians.
• Maintain essential study documents.
• Receive study medication and dispense per protocol.
• Maintain accountability logs for study medication.
• Assist in maintaining study supplies; ordering and storage.
• Read, learn, and pass required tests for GCP CFR IATA guidelines.
• Maintain records of all communications with sponsors, monitors, labs, etc.
• Use EMR system, Outlook, Word, Excel and related systems.
• Maintain continuing education for nursing licensure.
• Other duties as assigned.

Skills

Interpersonal skills

Communication

Teamwork

Multitasking

Tools

EMR system

Outlook

Word

Excel

MS Office

Job description

Urology Centers of Alabama seeks a Research Coordinator to manage screening, data collection, and protocol adherence across clinical studies. You will coordinate patient visits, tests, and sample handling while ensuring ICH/GCP, CFR, IATA, and HIPAA compliance within the study framework.

The role requires engagement with physicians and staff, attention to documentation accuracy, and timely communication with sponsors and monitors. Day shift, full-time on-site in Homewood, IL.