Clinical Research Associate: Site Monitoring & Study Delivery

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

Job summary

IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data quality according to protocol and regulations. You will manage site communications, training, and documentation, and coordinate with the project team to maintain timelines and deliverables.

Responsibilities include coordinating recruitment, handling regulatory submissions, and ensuring TMF/ISF readiness. Strong English skills and experience with GCP/ICH are required, along with proficiency in common trial

Qualifications

• Bachelor's degree in a scientific discipline or health care preferred.
• At least 2 years of independent on-site monitoring experience as a CRA.
• GCP and ICH guidelines knowledge.
• MS Word, Excel and PowerPoint proficiency; familiarity with clinical trial systems.
• Strong written and spoken English; good communication and problem-solving skills.

Responsibilities

• Perform site monitoring visits ( initiation, routine, close-out ).
• Monitor site recruitment plans to align with project needs.
• Administer protocol training and maintain site communications.
• Assess site quality and regulatory compliance; escalate issues.
• Track regulatory submissions, enrollment, CRFs, and data queries.
• Ensure documents are filed in TMF/ISF per local requirements.
• Collaborate with project team for execution and support.

Skills

Communication skills

Organizational skills

Time management

Financial management

English proficiency

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

EDC

CTMS

eTMF

IVRS/IWRS

Job description

IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data quality according to protocol and regulations. You will manage site communications, training, and documentation, and coordinate with the project team to maintain timelines and deliverables.

Responsibilities include coordinating recruitment, handling regulatory submissions, and ensuring TMF/ISF readiness. Strong English skills and experience with GCP/ICH are required, along with proficiency in common trial