Clinical Data Monitor I - Hybrid
Caris Life Sciences
August 13, 2026
Remote friendly (Irving, TX)
United States
Clinical Research and Development
Position Summary
The Clinical Data Monitor is responsible for clinical data management activities for Caris sponsored and collaborating protocols and projects. Ensures data integrity and quality to support oncology research. Provides support to external and internal research coordinators in patient enrollment, data collection, and data query resolution. Oversees and manages clinical investigative sites in accordance with Federal Code of Regulations, GCP, GRP, ICH Guidelines, local regulations, and applicable Compliance and Sponsor SOPs.
Job Responsibilities
- Maintain proficiency in Electronic Data Capture (EDC) systems (training, change proposals, user acceptance testing).
- Build and maintain relationships with site data and regulatory coordinators.
- Conduct QC review of Case Report Forms (CRFs), including source document verification and issuing data queries.
- Evaluate internal Clinical Research Coordinators in training; provide constructive feedback.
- Maintain regulatory documentation for assigned sites and study staff.
- Create and manage site records in the EDC for newly onboarded sites.
- Conduct quality control audits of the clinical database.
- Ensure compliance with GCP, FDA, IRB, HIPAA, site procedures, and ethical research standards.
- Confirm appropriate consenting is completed/documented prior to data abstraction.
- Communicate effectively with research teams, investigators, sponsors, and ancillary staff.
Required Qualifications
- 3–5 years data collection experience in a GCP-regulated clinical research environment.
- Proficient in Microsoft Office Suite; EDC experience.
- Oncology clinical study experience.
- Strong medical terminology; independent judgment.
- Organizational skills; ability to prioritize, meet deadlines, and manage multiple projects.
- Ability to build trust with site personnel; effective communication.
- High attention to detail; strong problem-solving.
- Excellent English written/verbal communication.
- Ability to propose/implement/evaluate issue resolutions.
Preferred Qualifications
- Bachelor’s degree.
- Research Coordinator certification (SoCRA, ACRP).
- Working knowledge of human anatomy.
Other
- May require occasional weekend/holiday work.
Conditions of Employment
- Successful completion of pre-employment background check, drug screening, credit check (for certain roles), and reference verification.
The Clinical Data Monitor is responsible for clinical data management activities for Caris sponsored and collaborating protocols and projects. Ensures data integrity and quality to support oncology research. Provides support to external and internal research coordinators in patient enrollment, data collection, and data query resolution. Oversees and manages clinical investigative sites in accordance with Federal Code of Regulations, GCP, GRP, ICH Guidelines, local regulations, and applicable Compliance and Sponsor SOPs.
Job Responsibilities
- Maintain proficiency in Electronic Data Capture (EDC) systems (training, change proposals, user acceptance testing).
- Build and maintain relationships with site data and regulatory coordinators.
- Conduct QC review of Case Report Forms (CRFs), including source document verification and issuing data queries.
- Evaluate internal Clinical Research Coordinators in training; provide constructive feedback.
- Maintain regulatory documentation for assigned sites and study staff.
- Create and manage site records in the EDC for newly onboarded sites.
- Conduct quality control audits of the clinical database.
- Ensure compliance with GCP, FDA, IRB, HIPAA, site procedures, and ethical research standards.
- Confirm appropriate consenting is completed/documented prior to data abstraction.
- Communicate effectively with research teams, investigators, sponsors, and ancillary staff.
Required Qualifications
- 3–5 years data collection experience in a GCP-regulated clinical research environment.
- Proficient in Microsoft Office Suite; EDC experience.
- Oncology clinical study experience.
- Strong medical terminology; independent judgment.
- Organizational skills; ability to prioritize, meet deadlines, and manage multiple projects.
- Ability to build trust with site personnel; effective communication.
- High attention to detail; strong problem-solving.
- Excellent English written/verbal communication.
- Ability to propose/implement/evaluate issue resolutions.
Preferred Qualifications
- Bachelor’s degree.
- Research Coordinator certification (SoCRA, ACRP).
- Working knowledge of human anatomy.
Other
- May require occasional weekend/holiday work.
Conditions of Employment
- Successful completion of pre-employment background check, drug screening, credit check (for certain roles), and reference verification.