Caris Life Sciences · 23 hours ago
Clinical Data Monitor I
United States
Full-time
Remote
Mid Level
$74K/yr - $84K/yr
3+ years expCaris Life Sciences is transforming cancer care by introducing precision medicine and improving the human condition across multiple diseases. The Clinical Data Monitor I is responsible for clinical data management activities, ensuring data integrity and quality to support oncology research efforts.
Artificial Intelligence (AI)BiopharmaBiotechnologyHealth CareLife Science
Responsibilities
Maintains proficient knowledge of Electronic Data Capture (EDC) systems to support training, change proposals, and user acceptance testing
Establish and maintain strong working relationships with site data and regulatory coordinators
Perform quality control review of submitted Case Report Forms (CRFs), including source document verification and issuance of data queries
Serve as an evaluator for internal Clinical Research Coordinators in training and provide detailed, constructive feedback
Maintain regulatory documentation for all assigned sites and study staff
Create and manage site records within the EDC for newly onboarded sites
Conduct quality control audits of the clinical database
Ensure compliance with GCP guidelines, FDA, Institutional Review Board (IRB), HIPAA regulations, site operating procedures, and ethical standards for the conduct of clinical research
Collaborate closely with onsite teams to confirm appropriate consenting is completed and documented prior to data abstraction
Communicate effectively with research teams, investigators, study sponsors, and ancillary staff
Qualification
Required
Requires 3-5 years of experience in data collection activities within a GCP regulated clinical research environment
Proficient in Microsoft Office Suite
Experience working with Electronic Data Capture (EDC) systems
Clinical study experience in oncology
Strong understanding of medical terminology
Ability to work independently and make sound decisions
Strong organizational skills with the ability to prioritize, meet deadlines, and manage multiple projects simultaneously
Demonstrated ability to build trust with site personnel and communicate effectively with diverse stakeholders
High attention to detail with a passion for contributing to meaningful research outcomes for patients
Strong problem solving skills and the ability to deliver practical solutions
Excellent written and verbal communication skills in English
Professional demeanor with positive, collaborative interactions with internal and external partners
Ability to propose, implement, and evaluate appropriate resolutions to issues
Preferred
Bachelor's degree preferred
Research Coordinator certification (SoCRA, ACRP)
Working knowledge of human anatomy
Benefits
Highly competitive and inclusive medical, dental and vision coverage options
Health Savings Account for medical expenses and dependent care expenses
Flexible Spending Account to pay for certain out-of-pocket expenses
Paid time off, including: vacation, sick time and holidays
401k match and Financial Planning tools
LTD and STD insurance coverages, as well as voluntary benefit options
Employee Assistance Program
Pet Insurance
Legal Assistance
Tuition Assistance
Company
Caris Life Sciences
Caris Life Sciences develops molecular profiling and AI-driven technologies to support precision medicine in oncology.
1001-5000 employees
Funding
Current Stage
Public CompanyTotal Funding
$1.86BKey Investors
BraidwellOrbiMedSixth Street
2025-06-18IPO
2025-04-07Private Equity· $168M
2023-01-19Debt Financing· $400M
Leadership Team
Luke Power
Chief Financial Officer
Brian Stengle
SVP, Chief Marketing Officer
Recent News
Labiotech UG
2026-01-17
2026-01-14
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