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Syneos Health looking for Regulatory Consultant

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Syneos Health looking for Regulatory Consultant

Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.

Post : Regulatory Consultant/Sr. Consultant - RIM/Veeva Business Analyst (US timeshift)

Job Description
General Responsibilities :
• Look for system/process-focused analysts with RIM/Veeva experience.
• Excellent communication and stakeholder management skills.
• Master’s degree with overall 8+ years’ experience
• Experience in system requirement gathering, validation, and user acceptance testing.
• Ability to collaborate across cross-functional teams (Reg Ops, IT, Process Development etc).

Note :
• Exclude candidates whose experience is limited to regulatory publishing/submissions.
• Availability in EST timezone for collaboration purposes.

Core Responsibilities :
• Act as the primary liaison between Regulatory Operations teams and IT/Tool Management teams.
• Focus on technology enablement and process optimization.
• Gather and document requirements from key users (business partners, RIM superusers, technical leads).
• Ensure requirements are maintained and updated in alignment with business needs.
• Collaborate with DTE and Validation teams.
• Support user testing activities, including preparation of test scripts and execution oversight.
• Serve as SME for RIM systems.
• Provide guidance, communication, and training to users on business tools and processes.
• Work closely with IT and process development teams to manage RIM system enhancements.
• Collaboration with global teams to coordinate system inputs, validate data, resolve missing fields or gaps, and support end-to-end system workflows.
• Contribute to continuous improvement initiatives.


Additional Information
Experience : 8+ years
Qualification : Master’s degree
Location : Gurugram-Hybrid
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 30th December 2025

Apply here for Regulatory Consultant


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