Site Research Assistant - Southfield, MI
About The Position
We are seeking a detail-oriented Research Assistant to support clinical trial activities in compliance with all applicable regulations. This role requires strong organizational skills, logical thinking, adaptability, and excellent interpersonal and team-building abilities. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
Requirements
- Minimum of an associate’s degree or equivalent education and experience
- At least 1 year of experience in a clinical research setting preferred
- Working knowledge of clinical trials and Good Clinical Practices (GCP)
- Familiarity with protocol-specific procedures, consent forms, and study schedules
- Proficiency in EDC entry and query resolution
- Experience in visit scheduling and regulatory binder upkeep
- Strong attention to detail and ability to prioritize tasks
- Excellent communication and relationship-building skills
- Applicable certifications and licenses as required by company, state, or regulatory bodies
- This position is not eligible for sponsorship.
Nice To Haves
- At least 1 year of experience in a clinical research setting preferred
Responsibilities
- EDC entry and query resolution
- Maintain regulatory binder and ensure compliance with documentation standards
- Schedule and coordinate subject visits and procedures
- Develop strong working relationships and maintain effective communication with study team members
- Build trust and respect with investigators and office staff
- Assist with screening, recruiting, and enrolling research subjects
- Perform patient/research participant scheduling and collect history
- Coordinate follow-up care and laboratory procedures
- Adhere to IRB-approved protocols and assist in informed consent processes
- Support the safety of research subjects
- Comply with company and Sponsor policies, SOPs, and guidelines
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees
