Clinical Research Coordinator — Hands-On Trials & Patient Care

Regulatory Jobs; Southfield (MI); Vor Ort; USD 48.000 - 58.000; Vollzeit

Zusammenfassung

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Southfield, MI. You will perform clinical procedures (ECGs, sample collection, vital signs), coordinate studies, and ensure GCP compliance while supporting participants throughout the research process.

Ideal candidates have a Bachelor’s degree or equivalent experience, 1+ year of clinical research, and strong data management skills with EDC systems.

Qualifikationen

• Bachelor’s degree preferred or equivalent education and relevant experience.
• Minimum 1+ year of clinical research experience.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Experience conducting patient study visits and participant-facing clinical research activities.
• Proficiency with EDC systems, including accurate data entry, query resolution, and data management processes.
• Strong attention to detail and ability to establish effective working relationships.

Aufgaben

• Perform a variety of clinical procedures, including ECGs, sample collection, and vital signs assessments.
• Coordinate clinical research studies and maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines.
• Conduct patient study visits and support participants throughout the research process, ensuring a positive study experience.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, evaluating eligibility based on study inclusion and exclusion criteria while ensuring their safety and well‑being throughout the study.
• Collect, enter, and maintain accurate clinical data in case report forms (CRFs) and Electronic Data Capture (EDC) systems.
• Assist with EDC query management and resolution, working closely with investigators and monitors to ensure data accuracy, completeness, and quality.
• Collaborate with investigators, sponsors, and study monitors to address study‑related issues and maintain high standards of data integrity.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Kenntnisse

Clinical research

GCP knowledge

EDC systems

Patient visits

Data management

Attention to detail

Team collaboration

Ausbildung

Bachelor's degree preferred

Equivalent experience

Tools

EDC platforms

Jobbeschreibung

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Southfield, MI. You will perform clinical procedures (ECGs, sample collection, vital signs), coordinate studies, and ensure GCP compliance while supporting participants throughout the research process.

Ideal candidates have a Bachelor’s degree or equivalent experience, 1+ year of clinical research, and strong data management skills with EDC systems.