Instagram
youtube
Facebook

Site Research Assistant - Hammond, La

1 year years
$25.00 – $39.00
10 Aug. 29, 2025
Job Description
Job Type: Part Time Education: High School Diploma or equivalent. 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: Covington, Louisiana
Job Type: Part-Time
Work Arrangement: On-Site (Office-Based)
Scheduled Weekly Hours: 24 hours
Job ID: R1499521
Company: IQVIA
Also Available In: Additional locations


Position Summary:

Assist in the conduct of clinical trial activities in compliance with all applicable regulations. This role requires strong logical thinking, prioritization skills, adaptability to changing conditions, and excellent interpersonal and team-building abilities.


Key Responsibilities:

  • Perform Electronic Data Capture (EDC) entry and resolve data queries.

  • Develop and maintain effective communication and strong working relationships with study team members.

  • Foster trust and collaboration with investigators and office staff to bridge clinical and research teams.

  • Assist in screening, recruiting, and enrolling research subjects.

  • Schedule patients/research participants for study visits.

  • Collect patient/research participant medical history.

  • Coordinate follow-up care and laboratory procedures.

  • Adhere strictly to IRB-approved study protocols.

  • Assist in obtaining informed consent from research subjects.

  • Ensure the safety and welfare of research subjects.

  • Coordinate protocol-specific research procedures, study visits, and follow-up care.

  • Comply with company and sponsor policies, SOPs, and guidelines.

  • Schedule subject visits and procedures efficiently.


Qualifications:

  • High School Diploma or equivalent.

  • Minimum 1 year relevant clinical research experience preferred.

  • Knowledge of clinical trials and principles of Good Clinical Practice (GCP).

  • In-depth understanding of protocol and study-specific operating procedures, consent forms, and study schedules.

  • Skillful in performing required clinical procedures.

  • Working knowledge of medical terminology.

  • Detail-oriented with strong organizational skills.

  • Ability to establish and maintain effective relationships with coworkers, managers, patients, physicians, and clients.

  • Applicable certifications/licenses as required by regulatory bodies.

  • Note: This position is not eligible for sponsorship.


Compensation:

  • Hourly Pay Range: $25.00 – $39.00
    (Varies based on qualifications, location, and schedule)

  • May include incentive plans, bonuses, and other benefits depending on eligibility.


About IQVIA:

IQVIA is a global leader in clinical research services and healthcare intelligence, connecting data and technology to accelerate medical innovation.
🔗 Learn more at https://jobs.iqvia.com


Equal Opportunity Employer:

IQVIA provides equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other protected status.
🔗 Details: https://jobs.iqvia.com/eoe


How to Apply:

Search Job ID: R1499521 or use the Apply Now button on the IQVIA careers page.