Clinical Study Documentation Specialist

Job overview

The Clinical Study Documentation Specialist is an onsite role based in Phoenix, AZ, with compensation not specified. This position provides critical support for Caris-sponsored clinical studies and collaborative research initiatives. The role exists to ensure that all clinical study documentation is maintained in compliance with regulatory requirements and internal standard operating procedures. By managing IRB submissions and study files, the specialist facilitates the smooth execution of clinical trials.

What you'll do

• Supports initiation and maintenance of clinical trials by preparing and submitting study documents to IRBs.
• Maintains accurate clinical study files, including staff certifications and training records.
• Coordinates with internal teams and research sites to ensure study documents are current, complete, and compliant.

What we're looking for

Skills & competencies

full-time

day shift

phoenix az

clinical research

documentation

regulatory

onsite

no on-call

clinical trials

precision medicine

Work arrangement

• Weekend coverage required

Why this role

Specialized focus on clinical regulatory documentation and IRB coordination for precision medicine trials.

About the employer

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