Site Research Assistant
Location: Shelby, North Carolina
Job Type: Part-time, Office-based
Job ID: R1504963
Weekly Hours: 16 Hours
Job Overview
The Site Research Assistant will support the conduct of clinical trial activities in compliance with all applicable regulations. This role requires logical thinking, adaptability, strong interpersonal skills, and the ability to prioritize tasks effectively. The position focuses on assisting study teams, engaging with patients, and ensuring compliance with protocols and SOPs.
Key Responsibilities
Data Management & EDC
Enter data into Electronic Data Capture (EDC) systems and resolve queries.
Maintain accurate and timely data in compliance with study protocols.
Patient Interaction & Study Coordination
Assist with screening, recruiting, and enrollment of research participants.
Schedule participant visits and study-related procedures.
Collect patient history and coordinate follow-up care and laboratory procedures.
Support informed consent process and ensure participant safety.
Coordinate protocol-related research procedures and study visits.
Communication & Collaboration
Develop and maintain strong working relationships with study team members, investigators, and office staff.
Facilitate clear communication to build trust between the clinic and research office.
Compliance & Documentation
Adhere to IRB-approved protocols, SOPs, and Sponsor policies.
Apply Good Clinical Practice (GCP) guidelines in all research activities.
Maintain knowledge of protocol-specific operating procedures, consent forms, and study schedules.
Qualifications
Education & Experience
High School Diploma or equivalent, plus 1 year relevant clinical research experience.
Preferred: 1+ year working in a clinical research setting.
Skills & Knowledge
Working knowledge of clinical trials and GCP principles.
Familiarity with medical terminology.
Ability to perform required clinical procedures accurately.
Attention to detail and strong organizational skills.
Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
Certifications & Licenses
Applicable certifications and licenses as required by the company, state, or regulatory bodies.
Additional Information
This position is not eligible for sponsorship.
On-site role (#LI-CES, #LI-DNP, #LI-HCP, #ONSITE).
Compensation & Benefits
Hourly Pay Range: $25.00 – $39.00 per hour (may vary based on qualifications, experience, and location).
Potential incentive plans, bonuses, and benefits in addition to base pay.
Employer
IQVIA – A global leader in clinical research services, commercial insights, and healthcare intelligence. Learn more at IQVIA Careers
.
Equal Opportunity Employer: IQVIA provides employment consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected status.
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