Senior Principal Clinical Programmer (Medidata RAVE)

2 hours ago

Hyderābād, IndiaStaff+

Responsibilities

Lead clinical programming tasks and deliverables across individual studies and large study programs.
Provide technical support and subject matter expertise for Medidata RAVE, Oracle clinical data tools, SAS, and related applications.
Design, develop, validate, maintain, and document clinical programming solutions for EDC builds, databases, edit checks, migrations, imports, exports, listings, and custom reports.
Monitor application performance, workflow alerts, system errors, and programming defects, and coordinate troubleshooting and resolution.
Lead system integrations, application updates, implementations, and user acceptance testing.
Coordinate project development activities, timelines, scope, budgets, metrics, resources, and change orders across multiple studies.
Represent the department in client meetings, bid defenses, sponsor audits, project reviews, and senior management status updates.
Provide senior review of program-level and multi-study deliverables for accuracy and quality.
Manage application vendors, service-level metrics, upgrades, new modules, documentation, and escalations.
Mentor, train, supervise, and support clinical programmers, including assigning work, reviewing workloads, and supporting staff development.
Lead process improvements, standardization tools, updated procedures, and new clinical programming concepts and technologies.
Attend study Quick Start Camps in the lead Clinical Programmer role and travel minimally as required.

Bachelor's degree required; a master's degree is preferred, and equivalent related education and experience may substitute for the bachelor's degree.
At least 8 years of experience with Medidata RAVE, including experience serving as a RAVE subject matter expert.
Experience with RAVE Core Configuration changes, migration, EDC build, complex custom functions, and technical exposure to Data Studio.
Working experience with a clinical Metadata Repository (MDR).
Experience training and mentoring team members and providing clinical trial process mentorship.
Ability to manage multiple priorities in a highly dynamic, matrix-structured environment.
Strong written, verbal, communication, interpersonal, analytical, and customer-facing skills.
Proficiency with Microsoft Office Suite, email, and voicemail.
Preferred programming experience with PL/SQL, SAS, C#, or VB.
Ability to read, write, speak, and understand English.

Career development and progression opportunities, supportive line management, technical and therapeutic area training, peer recognition, and a total rewards program.
Inclusive culture and opportunities to collaborate with colleagues across global clinical solutions teams.
Minimal travel may be required.

C#Sass

10,000+ employees