Clinical Study Programmer
Job Summary
A company is looking for a Clinical Study Build Programmer responsible for programming and testing clinical trial data collection databases.
Key Responsibilities:
- Program and test data collection systems and mappings for clinical trials
- Ensure accurate and efficient delivery of data collection systems aligned with study objectives
- Lead complex cross-functional projects and support regulatory activities
Required Qualifications:
- Master's degree with 5 years of experience in database programming or system validation, or Bachelor's degree with 7+ years of experience
- Knowledge of regulatory guidelines such as GCP and 21 CFR Part 11
- Experience with clinical technologies including CTMS and EDC
- Minimum 4 years' oncology experience preferred
- Project and vendor management experience
COMPLETE JOB DESCRIPTION
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