Clinical Research Associate: Site Monitoring & Trials

IQVIA; Afton (WY); On-site; USD 75,000 - 198,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate to perform site monitoring and ensure protocol adherence across study sites. You will manage recruitment plans, training, and regular communications with sites to meet sponsor and regulatory requirements.

Requires 2+ years on-site CRA experience, knowledge of GCP/ICH, and proficiency with EDC/CTMS/eTMF; strong English communication and organizational skills are essential.

Qualifications

• Requires knowledge of GCP and ICH guidelines.
• Effective written and verbal English communication.
• Strong organizational and problem-solving abilities.
• Experience with EDC, CTMS, eTMF and related systems.

Responsibilities

• Perform site monitoring visits per scope of work and GCP.
• Collaborate with sites to drive recruitment and data reporting.
• Train sites on protocol and conduct regular communications.
• Monitor regulatory submissions, approvals, and data queries.
• Maintain TMF and ISF documentation.
• Support project start-up and site financial management when applicable.

Skills

GCP

ICH guidelines

English proficiency

Organizational skills

Time/financial management

Communication skills

Education

Bachelor's Degree in scientific discipline or health care

Tools

EDC

CTMS

eTMF

IVRS/IWRS

MS Word

MS Excel

PowerPoint

Job description

IQVIA is seeking a Clinical Research Associate to perform site monitoring and ensure protocol adherence across study sites. You will manage recruitment plans, training, and regular communications with sites to meet sponsor and regulatory requirements.

Requires 2+ years on-site CRA experience, knowledge of GCP/ICH, and proficiency with EDC/CTMS/eTMF; strong English communication and organizational skills are essential.