Note: The job is a remote job and is open to candidates in USA. ProPharma provides consulting solutions across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology to support biotech, medical device, and pharmaceutical organizations. The Senior Clinical Data Coordinator supports Phase I-III clinical trials by reviewing and reconciling clinical data, testing and quality-controlling clinical databases, and maintaining data management documentation in accordance with applicable clinical practice standards.
Responsibilities
- Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database
- Perform User Acceptance Testing (UAT) of clinical databases
- Perform Quality Control (QC) of clinical databases
- Perform ongoing updates of Data Management-related documentation, as needed
Skills
- Minimum of 3 years of data management experience is required
- Experience with Electronic Data Capture (EDC) system(s) is required
- Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered
- Experience with Oracle Inc.'s Inform™ EDC system is preferred
- Oncology and/or inflammatory therapeutic area experience is preferred
Benefits
- Remote working supported
- Hybrid working encouraged for new hires based within a reasonably short commute of a ProPharma office, with time spent working from that office as agreed with the manager
- Diversity, equity, and inclusion commitment
- Safe and empowering workplace where employees can be their authentic selves
- Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits
- All applications are personally reviewed by a member of the recruitment team
- Applicants will always receive an outcome on their application
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