Clinical Research Coordinator - West Palm Beach, FL

$72,800 - $99,840/Yr

IQVIA - West Palm Beach, FL

Part-time - Entry Level

West Palm Beach, FL

5,001-10,000 employees

Professional, Scientific, and Technical Services

About the position

The Clinical Research Coordinator at IQVIA is responsible for overseeing and coordinating clinical research studies, ensuring the safety and well-being of study volunteers while adhering to regulatory standards and protocols. This role involves performing clinical procedures, maintaining high standards of care, and collaborating with the study team to ensure the successful execution of research projects.

Responsibilities

• Perform a variety of complex clinical procedures on subjects including ECG, sample collection, spirometry, and vital signs.
• Coordinate clinical research studies conducted by a supervising principal investigator.
• Update and maintain skills, training, and knowledge of current best nursing practices and topics related to clinical research.
• Safeguard the well-being of the subjects and ensure high standards are maintained.
• Maintain a safe environment in accordance with Health and Safety policies.
• Act as a volunteer advocate and address volunteer and visitor concerns proactively.
• Assist staff in clinical coordinator practices and the delivery of care to the volunteer.
• Report any deviation from normal practice to senior staff.
• Review study protocol, case report forms, and other study documents.
• Participate in project meetings with the project team as needed.
• Perform clinical set-up and preparation for the study, including labeling specimen collection tubes and setting up equipment.
• Plan logistical activity for procedures as per protocol.
• Generate volunteer instructions and obtain required supplies and equipment.
• Prepare and deliver study-specific training materials and documents.
• Troubleshoot study issues and participate in huddles to ensure daily tasks are executed to expected standards.
• Assist with data quality checking and query resolution to ensure data accuracy and completeness.
• Recruit and screen volunteers for inclusion in the study based on pre-determined criteria.
• Orient volunteers to the study and the site, including the purpose of the study and practical issues.
• Responsible for the correct administration and custody of study drug according to site standard operating procedures.
• Collect, record, and report clinical data and findings appropriately in case report forms.
• Collaborate closely with the study investigator on relevant adverse events and serious adverse events according to procedures outlined in the protocol.
• Cooperate with the study monitor and reserve time for questions during monitoring.
• Follow ICH GCP guidelines regarding all study and patient activities.

Requirements

• High School Diploma and 1 year of relevant work experience in clinical research.
• At least 1 year experience working in a clinical research setting preferred.
• Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
• Working knowledge of clinical trials and principles of Good Clinical Practices (GCP).
• In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
• Skill in carrying out required clinical procedures and working knowledge of medical terminology.
• Ability to pay close attention to detail and establish effective working relationships with coworkers, managers, patients, physicians, and clients.

Benefits

• Health insurance
• 401k plan
• Paid time off
• Professional development opportunities