Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Daily Responsibilities: Provide L2 system support for Veeva Vaults Manage system users, roles, and permissions Provide advisory/consultant expertise and support Drive continuous improvements by staying on top of new functionality Serve as escalation point for issues and
About the Role/Project We are seeking an Associate Consultant who can transition to Veeva. Flexibility and willingness to learn are essential. The initial focus will be functional support for Veeva applications, partnering with end users and stakeholders to
Regulatory Moderator Location: Remote – Philippines Employment Type: Full-time | 12-Month Fixed-Term Contract (with the possibility of extension) Start Date: ASAP About the Opportunity: Kelly is partnering with a leading global MedTech organisation to recruit an
Work Setup: Willing to work full onsite during training and hybrid (3x onsite per week) upon production in Taguig Work Schedule: Night shift Start Date: Nov 3, 2026 Requirements: Educational Attainment - Graduate of any of
About the Role/Project The resource will act as a Validation Consultant either for the client or for NNIT. Key responsibilities are ensuring compliance with regulatory requirements, company Computer Systems Validation (CSV), lifecycle procedures, manufacturing execution systems