Oncology Clinical Data Monitor

Caris MPI, Inc.; Irving (TX); On-site; USD 74,000 - 84,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Health Savings Account

401k match

Job summary

Caris Life Sciences is seeking a Clinical Data Monitor to oversee clinical data management for Caris-sponsored and collaborating protocols. You will support data integrity and quality to enhance oncology patient outcomes and assist both internal and external research coordinators in enrollment, data collection, and query resolution.

The role requires GCP experience, strong data handling skills, and collaboration with regulatory teams to ensure compliant and timely data delivery.

Qualifications

• 3-5 years of data collection experience in a GCP-regulated clinical research environment.
• Proficient in Microsoft Office Suite.
• Experience with Electronic Data Capture (EDC) systems.
• Clinical study experience in oncology.
• Strong understanding of medical terminology.

Responsibilities

• Oversight and management of clinical investigative sites in line with CFR, GCP, GRP, ICH guidelines and sponsor SOPs.
• Maintains proficiency with EDC systems to support training, change proposals, and UAT.
• Establish and maintain relationships with site data and regulatory coordinators.
• Perform quality control reviews of CRFs, including source document verification and data queries.

Skills

EDC systems

Microsoft Office

Oncology studies

Medical terminology

Independent work

Education

Bachelor's degree preferred

SoCRA/ACRP certification

Tools

EDC software

Microsoft Office Suite

Job description

Caris Life Sciences is seeking a Clinical Data Monitor to oversee clinical data management for Caris-sponsored and collaborating protocols. You will support data integrity and quality to enhance oncology patient outcomes and assist both internal and external research coordinators in enrollment, data collection, and query resolution.

The role requires GCP experience, strong data handling skills, and collaboration with regulatory teams to ensure compliant and timely data delivery.