Clinical Research
Clinical Data Coordinator (Clinical Trials & Registries)
Key Responsibilities
- Administer electronic data capture (EDC) systems (Medidata Rave, REDCap) for multi-site clinical trials and patient disease registries.
- Perform comprehensive clinical trial data validation, query generation, and discrepancy resolution in compliance with GCP and FDA guidelines.
- Coordinate with principal investigators, clinical research coordinators, and trial monitors to ensure timely database lock and milestone delivery.
- Validate electronic Case Report Forms (eCRFs) and track Serious Adverse Event (SAE) reporting to safety monitoring committees.
What We Are Looking For
- Bachelor's degree in Life Sciences, Nursing, Pharmacology, or Health Sciences.
- 3+ years of clinical data management or clinical trial coordination experience in pharma, biotech, or academic medical centers.
- Thorough understanding of Good Clinical Practice (GCP), ICH guidelines, 21 CFR Part 11, and CDISC standards (SDTM/CDASH).
- Exceptional attention to detail and rigorous commitment to clinical protocol compliance.
Core Technologies & Methodologies
Clinical Trials
Electronic Data Capture (EDC)
Medidata Rave
REDCap
GCP / FDA Guidelines
CDISC
eCRF Data Validation
Why Build Your Career at Oakbridge?
Elite Toolsets
Direct architecture experience with Domo, Snowflake, Databricks, AWS, dbt, and modern LLM APIs.
Remote Autonomy
High-trust asynchronous collaboration, flexible hours, and healthy work-life integration.
Paid Certifications
100% funded Domo, Snowflake SnowPro, and AWS Solution Architect certifications.
Competitive Pay
Above-market salary tiers, performance bonuses, and dedicated modern hardware stipends.