Lead programming for clinical databases and applications from study start to post database lock.
Collaborate with Data Management, Project Management, EDC vendors, clients and third-party vendors.
Provide training to end users and junior staff; estimate scope, schedule, and resource needs.

🎯 Requirements

Minimum 8 years’ experience; Bachelor’s degree or related experience.
Strong experience in Oncology; Autoimmune disease experience a plus.
Experience with Rave and Veeva; proficiency in Microsoft Office.
Proficiency in Object Oriented Programming (C#, C++, VB).
Understanding of CDISC standards (CDASH, SDTM, ADaM);}
Proficiency with more than one CDMS system; ability to troubleshoot and support peers.

🎁 Benefits

Regular full-time opportunity with remote work from European locations.

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