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Site Research Assistant - Arlington, Va

1+ years
Not Disclosed
10 April 29, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Site Research Assistant
Location: Arlington, Texas
Job ID: R1479193
Job Type: Part Time


Job Overview:

The Site Research Assistant will support the clinical trial process by assisting with patient recruitment, scheduling, data entry, and ensuring adherence to study protocols. The role requires strong interpersonal and team-building skills, along with the ability to adapt quickly to changing conditions.


Responsibilities:

  • EDC Entry & Query Resolution: Manage electronic data capture (EDC) and resolve queries to maintain data accuracy.

  • Team Collaboration: Develop and maintain effective communication with study team members, investigators, and office staff.

  • Patient Recruitment: Assist in the screening, recruiting, and enrollment of research subjects.

  • Scheduling & Coordination: Coordinate participant visits, lab procedures, and follow-up care.

  • Protocol Adherence: Ensure all activities comply with the IRB-approved protocol and company policies.

  • Informed Consent: Support the informed consent process, ensuring participants understand their role in the study.

  • Safety & Well-being: Monitor the safety of research participants throughout the study.

  • Study Visits: Assist in coordinating and scheduling study visits and protocol-related procedures.


Qualifications:

  • Education: High School Diploma required, with 1+ years of relevant clinical research experience.

  • Experience: At least 1 year in a clinical research setting preferred.

  • Skills: Knowledge of clinical trials, Good Clinical Practices (GCP), and medical terminology. Ability to manage multiple tasks and maintain attention to detail.

  • Certifications: Applicable certifications and licenses required by regulatory bodies.


Compensation:

  • Hourly Rate: $25.00 - $39.00 per hour (Based on experience and qualifications).

  • Additional benefits, including incentive plans, bonuses, and health/welfare plans, may be offered.


About IQVIA:
IQVIA is a leading provider of clinical research services, helping accelerate the development of innovative medical treatments to improve patient outcomes.

Visit Careers at IQVIA


Equal Opportunity Employer:
IQVIA is committed to diversity and equal opportunity in employment.