
Senior Clinical Research Professional
1 day ago
Transforming the Clinical Research Landscape
This role offers a unique opportunity to contribute to the success of our clinical research initiatives.
- Perform User Acceptance Testing (UAT) for CRF screens, database edit checks, and reports/listings.
- Test clinical study setup configurations including protocol parameters, visit schedules, and form designs.
- Validate external data acquisition and ensure accurate processing.
- Collaborate with Clinical Data Scientists and Study Data Managers to understand study scope and expectations.
- Strong experience with clinical study setup and CDMS platforms and CTMS required.
- Review edit check specifications; write and execute UAT scripts.
- Conduct QC on metadata listings and peer review of programming checks.
- Support automation tool validation and standardization of test scripts.
- Ensure consistent use of clinical data standards across programs and repositories.
- Work with Clinical Data Management Systems (e.g., Medidata Rave, Oracle InForm) to validate database builds and data flows.
- Ensure compliance with GxP/GcP and internal SOPs.
- Document and share study-related testing deliverables and lessons learned.
This position requires a solid understanding of SDLC, validation methodology, and document management.
Key Qualifications:
- Proven experience in clinical research operations.
- Strong technical skills in CDMS and CTMS platforms.
- Excellent collaboration and communication skills.
- Ability to work independently and as part of a team.
- Attention to detail and ability to manage multiple priorities.
What We Offer:
- Competitive compensation package.
- Opportunities for career growth and professional development.
- A collaborative and dynamic work environment.
Join Our Team:
We are committed to fostering a culture of innovation, inclusivity, and excellence. If you are passionate about clinical research and want to make a meaningful contribution, we encourage you to apply for this exciting opportunity.
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