Job Title: Site Research Assistant
Location: Brooklyn, NY (Job listed under New York, New York)
Job ID: R1470449
Job Type: Part Time
Work Set-Up:
On-site
Scheduled Weekly Hours: 24
Job Profile Summary:
The Site Research Assistant will support clinical trial activities in compliance with applicable regulations. This role requires logical thinking, prioritization, adaptability, and strong interpersonal/team-building skills.
Responsibilities:
Enter data in Electronic Data Capture (EDC) systems and resolve queries
Maintain effective communication with study team, investigators, and office staff
Assist in screening, recruiting, and enrolling research participants
Schedule participant visits and procedures
Collect participant histories and coordinate lab procedures
Ensure protocol adherence as approved by the IRB
Assist in the informed consent process
Support participant safety
Coordinate study-related procedures, visits, and follow-up care
Comply with sponsor and company SOPs and guidelines
Qualifications:
High School Diploma and 1 year of relevant clinical research experience (or equivalent education/experience)
At least 1 year of experience in a clinical research setting preferred
Knowledge of clinical trials and GCP guidelines
Understanding of study protocols, SOPs, consent forms, and schedules
Competency in clinical procedures and medical terminology
Strong attention to detail
Ability to build and maintain professional relationships
Certifications/licenses as required by regulatory bodies
Note: This role is not eligible for sponsorship
Compensation:
Hourly Rate: $25.00 – $39.00 (based on qualifications, experience, and location)
Additional Benefits: May include bonuses, incentives, and a variety of health and welfare benefits
About IQVIA:
IQVIA delivers clinical research services and healthcare intelligence globally, accelerating the development and commercialization of innovative treatments to improve health outcomes. Learn more at IQVIA Careers
Equal Opportunity Employer:
IQVIA offers equal employment opportunities to all applicants regardless of race, religion, gender, sexual orientation, veteran status, or disability.
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