Site Research Assistant - Flint, MI
IQVIA
Summary
We are seeking a Research Assistant (RA) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Job description
About the Role
We are seeking a Research Assistant (RA) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
- Perform accurate EDC data entry, manage queries, and ensure timely resolution.
- Maintain and update the regulatory binder in compliance with documentation and audit standards.
- Coordinate and schedule subject visits, procedures, and follow-up activities.
- Build effective working relationships with investigators, clinical staff, and study team members.
- Support subject screening, recruitment, and enrollment activities.
- Assist with patient/research participant scheduling and collection of medical history.
- Coordinate lab procedures and follow-up care in alignment with study protocols.
- Ensure strict adherence to IRB-approved protocols, including assistance with informed consent processes.
- Uphold participant safety and report concerns promptly per SOPs and Sponsor requirements.
- Follow all company policies, SOPs, guidelines, and Good Clinical Practice (GCP) standards.
Qualifications
- Associate degree preferred or equivalent combination of education and relevant experience.
- 1+ years of experience in a clinical research environment preferred.
- Strong working knowledge of clinical trials, GCP, and protocol-specific procedures.
- Proficiency with EDC systems, data entry accuracy, and query management.
- Experience with visit scheduling, regulatory documentation, and binder maintenance.
- Excellent attention to detail, time management, and task prioritization.
- Strong communication, interpersonal, and relationship-building skills.
Requirements
- Associate degree preferred or equivalent combination of education and relevant experience.
- 1+ years of experience in a clinical research environment preferred.
- Strong working knowledge of clinical trials, GCP, and protocol-specific procedures.
- Proficiency with EDC systems, data entry accuracy, and query management.
- Experience with visit scheduling, regulatory documentation, and binder maintenance.
- Excellent attention to detail, time management, and task prioritization.
- Strong communication, interpersonal, and relationship-building skills.
Benefits
- Health and welfare benefits
Company overview
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Headquartered in Durham, North Carolina, the company operates in over 100 countries with approximately 86,000 employees worldwide. IQVIA specializes in creating intelligent connections across all aspects of healthcare through its proprietary IQVIA Connected Intelligence platform, which combines analytics, transformative technology, big data resources, and extensive domain expertise. The company's comprehensive portfolio includes clinical trial management, real-world evidence generation, commercial insights, and regulatory compliance services. IQVIA serves a diverse client base including pharmaceutical manufacturers, biotechnology companies, medical device firms, government agencies, and healthcare providers. With its Healthcare-grade AI capabilities and extensive global data assets, IQVIA accelerates the development and commercialization of innovative medical treatments while improving healthcare outcomes for patients globally. The company is publicly traded on the New York Stock Exchange under the ticker symbol IQV.