We are seeking a detail-oriented Clinical Trial Technology Associate to manage, configure, and support our suite of clinical eClinical applications. In this role, you will bridge the gap between clinical operations and technology, ensuring that critical data platforms run smoothly, remain compliant, and support effective trial execution.
Key Responsibilities
- System Administration: Configure, maintain, and support core eClinical systems, including EDC, CTMS, and eTMF platforms.
- User Support & Training: Provide technical troubleshooting, manage user access permissions, and deliver system training to internal teams and external site staff.
- Data & Testing: Assist with User Acceptance Testing (UAT), system integrations, and system validation workflows to ensure high data integrity.
- Compliance & Quality: Maintain strict adherence to ICH-GCP guidelines, 21 CFR Part 11, and data privacy standards (GDPR/HIPAA).
Qualifications
- Bachelors degree in Life Sciences, Biotechnology, Microbiology Information Technology, or a related field.
- Prior experience or foundational knowledge in clinical research operations and clinical data management.
- Familiarity with industry-standard software such as Medidata Rave, Veeva Vault, or Oracle Clinical is highly preferred.
- Strong analytical, communication, and technical troubleshooting skills.