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This role aligns with Accenture’s Life Sciences R&D vertical, supporting the end-to-end lifecycle of clinical trials and clinical data management. As a new associate, you will work on activities critical to the smooth collection, integration, and management of clinical data, contributing to advancements in biopharma and patient care.
Key Responsibilities
- Database Testing: Design, test, and validate EDC (Electronic Data Capture) databases for clinical trials.
- User Acceptance Testing (UAT): Create and maintain UAT procedures, including test plans, reports, and verification of database requirements (eCRFs, edit checks, extractions).
- Data Management Operations: Perform query generation, discrepancy reviews, and ensure proper data reconciliation.
- CRF Completion Guidelines (CCG): Develop and maintain guidelines for Clinical Research Forms (CRF) and Serious Adverse Event (SAE) reconciliation.
- Protocol Compliance: Identify and flag protocol deviations within the clinical database and validate compliance through edit check testing.
- Team Collaboration: Work under the guidance of your supervisor, contributing to a small team with clear goals and instructions.
What We Are Looking For
- Education: Bachelor’s in Engineering (BE) or equivalent.
- Experience: 0 to 1 year (fresh graduates welcome).
- Skills Required:
- Basic understanding of clinical data management and testing protocols.
- Ability to design and test EDC databases and perform UAT procedures.
- Problem-solving abilities and attention to detail.
- Effective teamwork and communication skills.
- Adaptability to rotational shifts.
Skills That Will Set You Apart
- Familiarity with clinical trial processes and regulatory guidelines.
- Experience with CRF/eCRF design and edit checks.
- Knowledge of data extraction and discrepancy management tools.
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