Clinical Trials Research Assistant – Onsite, Part-Time

IQVIA LLC; Pittsburgh (Allegheny County); On-site; USD 34,440 - 53,726; Part time

Job summary

IQVIA LLC is seeking a detail-oriented Site Research Assistant for their Pittsburgh location. This part-time role (24 hours per week) involves supporting clinical research studies, managing data entry, and ensuring compliance with regulatory standards.

The ideal candidate will have at least 1 year of clinical research experience and proficiency with EDC systems. Join us to contribute to innovative healthcare solutions!

Qualifications

• At least 1 year of experience in a clinical research environment is preferred.
• Working knowledge of GCP and protocol-specific procedures is necessary.
• Strong attention to detail and organizational skills are essential.

Responsibilities

• Perform accurate EDC data entry and manage data queries.
• Coordinate and schedule participant visits and follow-up activities.
• Ensure compliance with regulatory and quality standards.

Skills

EDC data entry

Clinical trials knowledge

Patient chart review

Regulatory documentation

Education

Associate degree or equivalent

Tools

EDC systems

Job description

IQVIA LLC is seeking a detail-oriented Site Research Assistant for their Pittsburgh location. This part-time role (24 hours per week) involves supporting clinical research studies, managing data entry, and ensuring compliance with regulatory standards.

The ideal candidate will have at least 1 year of clinical research experience and proficiency with EDC systems. Join us to contribute to innovative healthcare solutions!