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Cytel

Lead Database Development Specialist

Cytel, Dover, Delaware, United States, 19904

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We are seeking an experienced Medidata RAVE programmer to join our team as a Lead Database Development Specialist. This role involves maintaining the Rave URL and serving as the primary contact for teams utilizing Medidata applications such as CTMS, eCOA, and Safety Gateway. Become the Subject Matter Expert

on Medidata applications, providing expert advice and comprehensive training across various functional areas.

Ensure Consistency

by maintaining Core Configuration, focusing on efficiency across all studies.

Manage Cloud Admin EDC roles

to uphold consistency and efficiency across all studies.

Communicate Regularly

with teams about updates and potential impacts related to configurations and systems.

Assess Impact

of Medidata release notes and updates, delivering essential information on eLearnings and Rave reports to teams.

Act as a Liaison

between Sponsor and CRO programmers to foster collaboration and streamline processes.

Coordinate Data Collection

activities between Sponsor Data Management and Statistical Programming teams.

Collaborate Effectively

with business owners of other Medidata applications to enhance integration and functionality.

Requirements:

Minimum of 12 years of progressive clinical research experience.

Medidata Rave Certified Study Builder.

At least 10 years of experience as a database programmer.

Zelta certification is a plus but not mandatory.

Bachelor's Degree is required.

Cytel Inc. is an Equal Employment and Affirmative Action Employer. We encourage all applicants to apply regardless of race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other legally protected characteristic.