Clinical Trial Associate: Drive Study Operations & Compliance

Ardelyx; Newark (CA); On-site; USD 86,000 - 105,000; Full time

Benefits offered by this job

401(k) plan with generous employer match

12 weeks paid parental leave

Flexible time off

Job summary

Ardelyx is seeking a Clinical Trial Associate in Newark, California, to support clinical trial management. The ideal candidate will ensure compliance with ICH‑GCP, provide operational support, and maintain study documentation.

Key qualifications include a Bachelor’s degree in a scientific field and 2+ years of experience in clinical operations or research. A robust benefits package and an annual base pay range of $86,000 to $105,000 are offered.

Qualifications

• 2+ years of experience in Clinical Operations or clinical research.
• Working knowledge of the clinical trial lifecycle.
• Strong organizational skills and attention to detail.

Responsibilities

• Provide operational support for assigned clinical trial(s).
• Assist Clinical Trial Managers with day-to-day study activities.
• Ensure compliance with ICH-GCP and regulatory requirements.

Skills

Clinical Operations

Data verification

Microsoft Office applications

Project management tools

Education

Bachelor’s degree in scientific or related field

Tools

EDC systems

CTMS systems

eTMF platforms

Job description

Ardelyx is seeking a Clinical Trial Associate in Newark, California, to support clinical trial management. The ideal candidate will ensure compliance with ICH‑GCP, provide operational support, and maintain study documentation.

Key qualifications include a Bachelor’s degree in a scientific field and 2+ years of experience in clinical operations or research. A robust benefits package and an annual base pay range of $86,000 to $105,000 are offered.