Clinical Research Associate (CRA II/Senior) – Metabolic

Job overview

The Clinical Research Associate (CRA II/Senior) – Metabolic role is listed in Columbus, Ohio; the description says the role conducts onsite monitoring at assigned clinical sites and includes a remote-work hashtag. Compensation is not specified. The role supports Parexel’s patient-focused clinical trials. The associate manages clinical sites from identification through closeout, helping protect participant safety, maintain regulatory compliance, and ensure reliable study data. Site monitoring, issue resolution, recruitment support, and documentation oversight contribute to successful metabolic, MASH, or obesity study delivery.

What you'll do

• Conduct qualification, site initiation, monitoring, and termination visits and prepare visit reports
• manage site quality and delivery through closeout
• serve as the primary contact for assigned sites
• support study integrity and site relationships
• review trial performance and participant safety
• develop recruitment strategies with sites
• ensure compliance with protocols, Good Clinical Practice, and regulations
• evaluate data quality and investigational product accountability
• verify regulatory documentation.

What we're looking for

Skills & competencies

clinical research associate

cra ii/senior

metabolic

mash

obesity

clinical trials

site monitoring

good clinical practice

patient safety

parexel

columbus oh

Work arrangement

• Weekend coverage required

Benefits & perks

• Health, vision, and dental insurance
• tuition reimbursement
• vacation, holiday, and sick time
• flexible spending and health savings accounts
• 401(k) with company match
• pet insurance.

Why this role

Requires metabolic/MASH and/or obesity clinical trial monitoring experience and at least 18 months of direct onsite CRA monitoring experience.

About the employer

Parexel is hiring for this role. Industry: Research and Development in Biotechnology (except Nanobiotechnology). Sector: 54.