Remote Clinical Research Quality Control Associate

CenExel; Riverside (CA); Hybrid; USD 40,000 - 45,000; Full time

Benefits offered by this job

Health Insurance

Dental

Vision

LTD

STD

Life Insurance

401k

Job summary

CenExel Clinical Research is seeking a Clinical Research Quality Control Associate to ensure accuracy, consistency, and integrity of trial documentation across operations, data management, and regulatory teams.

You will review essential trial documents, support TMF practices, and assist with audits while adhering to FDA, EMA, and ICH guidelines in a collaborative, office-based setting. Remote work is part of the arrangement.

Qualifications

• Bachelor’s degree in life sciences, healthcare, or related field (preferred).
• 1–3 years of clinical research experience, with at least 1 year in QC/QA or documentation review.
• Familiarity with regulatory requirements (GCP, ICH, FDA, EMA).
• Experience with electronic systems such as eTMF, EDC, and CTMS preferred.
• Strong attention to detail and organizational skills.

Responsibilities

• Performs quality control reviews of clinical trial documents to ensure accuracy and consistency.
• Identifies discrepancies and follows up with teams for resolution.
• Supports preparation and QC of Trial Master File (TMF) documents.
• Assists in internal audits and inspection readiness activities.
• Collaborates with cross-functional teams to maintain high documentation standards.
• Maintains QC metrics and supports quality improvement initiatives.
• Ensures compliance with GCP, ICH, FDA/EMA and SOPs.

Skills

Communication skills

Attention to detail

Organizational skills

Teamwork

Education

Bachelor's degree in life sciences/healthcare or related field

Tools

eTMF

EDC

CTMS

Job description

CenExel Clinical Research is seeking a Clinical Research Quality Control Associate to ensure accuracy, consistency, and integrity of trial documentation across operations, data management, and regulatory teams.

You will review essential trial documents, support TMF practices, and assist with audits while adhering to FDA, EMA, and ICH guidelines in a collaborative, office-based setting. Remote work is part of the arrangement.