Data Coordinator - 252759

Data Coordinator•252759 at Medix Data Coordinator•252759 at Medix in WEST SACRAMENTO, California Posted in 3 days ago.

Type:

full-time

Job Description:

Job Title:

Data Coordinator•

Clinical Research Location:

Hybrid (Sacramento, CA) 1 day WFH per week

Schedule:

Full-Time, Monday•Friday, 8:00 AM•5:00

PM Compensation:

$35•$40/hour

Position Overview:

An established clinical research site is seeking a detail-oriented Data Coordinator to support a high-volume oncology trial portfolio. This individual will play a critical role in ensuring the accuracy, integrity, and timeliness of clinical trial data, while collaborating closely with clinical and regulatory teams. This is an excellent opportunity for someone with oncology research experience who enjoys working with complex datasets and contributing to meaningful, patient-centered research.

Responsibilities:

Accurately enter clinical trial data from electronic medical records (EMR) into Electronic Data Capture (EDC) systems Translate the full patient journey into study-specific databases, ensuring completeness and accuracy Serve as the primary point of contact for data queries from study monitors, investigating discrepancies and providing timely resolutions Ensure all data entry is completed within sponsor-required timelines (typically 3-5 business days post-visit) Assist in confirming patient eligibility by organizing and reviewing lab results, imaging, and pathology reports for Principal Investigator review Monitor medical records for adverse events, hospitalizations, or new symptoms and escalate appropriately to clinical staff Support study teams in maintaining accurate and up-to-date patient data throughout the trial lifecycle Maintain source documentation in a constant state of audit readiness Review study protocols to ensure all required procedures, visits, and assessments are completed within designated timeframes Support compliance with GCP, sponsor requirements, and internal quality standards

Qualifications:

Bachelor's degree required Minimum 2+ years of clinical research data experience at the site level Experience supporting oncology clinical trials strongly preferred Familiarity with EDC systems and EMR platforms

Preferred Qualifications:

ACRP or SoCRA certification Experience working in a high-volume research environment