Parexel Hiring Regulatory Affairs Labeling

Parexel, as a leading global clinical research organization (CRO), design and deliver clinical trials with the patient in mind. Parexel defines it by the difference it make in patients' lives and the compassion it bring to every aspect of our work. By fusing its expertise with Heart® philosophy, it achieve remarkable outcomes together.

Post : Regulatory Affairs Labeling

About the Role
• We are seeking a Regulatory Labeling Specialist to join our team in a remote capacity. As a Regulatory Labeling Specialist, you will ensure that medicinal product information remains accurate, compliant, and current throughout its lifecycle. Accurate labeling helps patients and healthcare professionals get the information they need about medicines. This position plays a key role in regulatory impact assessment, product information management, Health Authority submissions, and post-approval compliance. You will collaborate with cross-functional teams and client stakeholders, follow industry-standard processes, and contribute to regulatory and labeling operations from planning through post-approval activities.
• Responsibilities include assessing the regulatory impact of change controls, managing product information and labeling updates, preparing Health Authority submissions, and driving post-approval activities in Veeva RIMS, with opportunities to deepen your expertise and influence regulatory outcomes.
• You will join a fast-paced, growth-oriented environment focused on making a meaningful impact through regulatory impact assessment, product information management, and Health Authority submissions. With diverse teams and continuous learning opportunities, the Regulatory Labeling Specialist can explore career paths and expand skills across regulatory affairs.

Key Responsibilities
• Perform regulatory impact assessments for change controls raised in TrackWise for medicinal products registered via the Centralized Procedure (CP), Mutual Recognition Procedure (MRP), Decentralized Procedure (DCP), or National Procedure (NP)
• Manage product information updates, including creation and updates of the Company Core Data Sheet (CCDS), applying clinical expertise
• Prepare and submit variations, notifications, and renewals to Health Authorities
• Respond to Health Authority questions on submissions
• Coordinate labeling updates, including translations, with team members and client stakeholders
• Manage all required post-approval activities in Veeva Regulatory Information Management System (RIMS), including artwork updates

You'll thrive in this role if you bring :
• Strong coordination skills and the ability to work effectively with team members and client stakeholders
• Strong planning skills, including planning variation submissions so they are completed on time and to the required quality to meet KPIs
• Clear communication skills and a collaborative, team-oriented approach
• Experience working in clinical research, healthcare, or a regulated environment
• A patient-focused mindset and strong attention to detail
• Comfort working with Veeva RIMS and TrackWise

Candidate Profile
• Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field, or equivalent professional experience
• 6 +years of experience in regulatory affairs or regulatory labeling
• Knowledge of regulatory requirements and Health Authority submission processes for medicinal product labeling
• Clinical expertise to support product information and CCDS updates
• Knowledge of Veeva RIMS
• Fluent in English
• Strong communication, organization, and planning skills
• Experience with xEVMPD

Additional Information
Experience : 6 +years
Qualification : Bachelor's degree in Life Sciences, Pharmacy, Chemistry
Location : India, Remote
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory Affairs
End Date : 25th November 2026