Note: The job is a remote job and is open to candidates in USA. ProPharma provides consulting solutions across the pharmaceutical, biotechnology, medical device, clinical research, regulatory, quality, and pharmacovigilance product lifecycle. 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 guidelines and timelines.
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 work arrangement
- Hybrid work option for new hires based within a reasonably short commute of one of ProPharma's offices, as agreed with their manager
- A safe and inclusive workplace where employees are empowered to succeed
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