Clinical Research Associate II/Senior Clinical Research Associate - FSP

Job overview

The Clinical Research Associate (CRA) is an onsite role based in Salt Lake City, UT, responsible for site management and monitoring of clinical trials to ensure patient safety and protocol compliance. Compensation is not specified for this position, which supports the company's clinical research initiatives. This role exists to safeguard the quality of investigator sites and ensure effective delivery of clinical trials from activation through close-out. The CRA contributes to the team by managing investigator relationships, resolving protocol-related issues, and ensuring all study activities adhere to Good Clinical Practices (GCP) and sponsor standards.

What you'll do

• Manage site monitoring and close-out activities, ensure compliance with Study Monitoring Plan (SMP), serve as primary point of contact for investigator sites, perform site development and training, monitor adverse events, and maintain Trial Master File (TMF) documentation.

What we're looking for

Skills & competencies

full-time

day shift

salt lake city ut

parexel

clinical research

gcp

site monitoring

life sciences

onsite

travel required

Work arrangement

• Weekend coverage required

Benefits & perks

• Equal Opportunity Employer
• comprehensive benefits package.

Why this role

Requires 2+ years of monitoring experience; 60-80% travel required.

About the employer

Parexel is hiring for this role. Industry: Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology). Sector: 54.