About the role
Responsibilities
- Subject Matter Expert on Medidata applications who can advise and teach across functional areas
- Maintain Core Configuration, ensuring consistency and efficiency across all studies
- Maintain Cloud Admin EDC roles, ensuring consistency and efficiency across all studies
- Communicate updates/potential impacts on above to teams
- Communicate and assess impact of Medidata release notes, updates to eLearnings, Rave reports to teams
- Act as a liaison between Sponsor and CRO programmers
- Act as a liaison for data collection between Sponsor DM and Statistical Programming
- Work with business owners of other Medidata applications
Qualifications
- At least 8 years progressive Clinical Research Experience
- Medidata Rave Certified Study Builder
- 6 years’ experience as a database programmer
- Zelta certified builder a plus, but not a requirement
- Bachelors Degree Required
About Cytel
Cytel is the world’s leading data-science CRO, driving advancements in human health through robust analytics and innovative clinical trial software. For nearly four decades, we have set the standard in adaptive trial design, leveraging extensive data insights to inform strategy throughout every phase of drug development and commercialization. Our mission is clear: accelerate drug development, enhance success rates, and deliver better patient outcomes. With a comprehensive suite of services from innovative trial design to end-to-end biometrics and real-world evidence, our specialized, multidisciplinary team ensures optimal strategies for preclinical research, trial execution, market access, and reimbursement.
Headquartered in Cambridge, Massachusetts, Cytel has a global presence with over 2,000 employees across North America, Europe, and Asia. Learn more about how Cytel is harnessing the power of data to advance human health at www.cytel.com.
About the role
Responsibilities
- Subject Matter Expert on Medidata applications who can advise and teach across functional areas
- Maintain Core Configuration, ensuring consistency and efficiency across all studies
- Maintain Cloud Admin EDC roles, ensuring consistency and efficiency across all studies
- Communicate updates/potential impacts on above to teams
- Communicate and assess impact of Medidata release notes, updates to eLearnings, Rave reports to teams
- Act as a liaison between Sponsor and CRO programmers
- Act as a liaison for data collection between Sponsor DM and Statistical Programming
- Work with business owners of other Medidata applications
Qualifications
- At least 8 years progressive Clinical Research Experience
- Medidata Rave Certified Study Builder
- 6 years’ experience as a database programmer
- Zelta certified builder a plus, but not a requirement
- Bachelors Degree Required
About Cytel
Cytel is the world’s leading data-science CRO, driving advancements in human health through robust analytics and innovative clinical trial software. For nearly four decades, we have set the standard in adaptive trial design, leveraging extensive data insights to inform strategy throughout every phase of drug development and commercialization. Our mission is clear: accelerate drug development, enhance success rates, and deliver better patient outcomes. With a comprehensive suite of services from innovative trial design to end-to-end biometrics and real-world evidence, our specialized, multidisciplinary team ensures optimal strategies for preclinical research, trial execution, market access, and reimbursement.
Headquartered in Cambridge, Massachusetts, Cytel has a global presence with over 2,000 employees across North America, Europe, and Asia. Learn more about how Cytel is harnessing the power of data to advance human health at www.cytel.com.