Job Title: Site Research Assistant
Location: Sarasota, Florida
Job ID: R1480854
Job Type: Part Time (32 hours/week)
Work Set-Up: On-site
Job Overview:
The Site Research Assistant will support clinical trial operations in compliance with applicable regulations and study protocols. This role is crucial in maintaining accurate data collection, patient coordination, and adherence to Good Clinical Practices (GCP). Ideal candidates will possess strong organizational, interpersonal, and prioritization skills to thrive in a dynamic research environment.
Responsibilities:
Perform Electronic Data Capture (EDC) entry and resolve data queries.
Establish and maintain effective communication with study teams, investigators, and clinic staff.
Assist in screening, recruiting, and enrolling research participants.
Handle scheduling for patients and research procedures.
Collect medical histories and coordinate laboratory and follow-up care.
Support adherence to IRB-approved protocols and safety of participants.
Assist in the informed consent process.
Coordinate all protocol-related procedures and visits.
Comply with sponsor and company SOPs, guidelines, and regulatory requirements.
Qualifications:
Education & Experience:
High School Diploma with a minimum of 1 year relevant experience in clinical research required.
Experience in a clinical trial setting preferred.
Knowledge & Skills:
Understanding of clinical trial operations and GCP principles.
Familiarity with study protocols, informed consent, and clinical procedures.
Proficient in medical terminology.
High attention to detail and organizational skills.
Strong interpersonal communication and teamwork capabilities.
Certifications and licenses as required by regulatory bodies and company policies.
Compensation:
Hourly Rate Range: $25.00 – $39.00
Actual pay may vary based on experience, location, and qualifications. Incentives, bonuses, and benefits may be available depending on the role.
About IQVIA:
IQVIA is a global leader in clinical research and health analytics, committed to improving patient outcomes and advancing medical innovation through intelligent connections in the life sciences industry.
Equal Opportunity Employer:
All applicants will be considered fairly regardless of race, gender, religion, disability, veteran status, or other protected categories.
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