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Senior Regulatory Intelligence Associate
Primary Location: India, Remote Job ID R0000040060 Category Regulatory Affairs Date Posted 03/24/2026Overview
As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.
We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Problem-solver
- Relationship-builder
- Results-driven
- Strategic
About This Role
The primary purpose of this role is to maintain awareness of local and regional regulatory requirements through monitoring, analysis and interpretation to support both compliance and regional regulatory policy priorities.
- The Regulatory Intelligence Senior Associate is responsible for:
- Contributing to the delivery of regulatory intelligence and pharmacovigilance (PV) regulatory intelligence tailored to CLIENT priorities.
- Engaging with Global Regulatory Affairs & Safety (GRAS) staff, including affiliate-based Local Regulatory Representatives (LRRs) and Local Safety Officers (LSOs) and Regional Regulatory Leads (RRLs) and Regional Safety Officers (RSOs) as required.
- Monitoring and analysis of regulatory and PV regulatory safety updates (new and revised laws and regulatory information issued by health authorities) to support internal impact assessments.
- Management of impact assessment of new/revised regulatory and PV regulatory information, including engaging with local and global subject matter experts (SMEs) in accordance with company SOPs.
- Providing intelligence analysis and policy support tailored to CLIENT internal priorities, including preliminary analysis of potential impacts for CLIENT.
- Other tasks that may be assigned from time to time.
- The role is expected to work in coordination with similar roles in other regulatory jurisdictions, such that regulatory intelligence and PV regulatory intelligence activities are coordinated across the geographies in which CLIENT operates.
- The role reports to the Global Regulatory and Safety Policy & Intelligence (GRASP) team.
Contribute to delivery of regulatory intelligence and pharmacovigilance (PV) regulatory intelligence
Delivery of consolidated regulatory/PV regulatory intelligence in accordance with company expectations.
Regulatory/PV Regulatory Impact Assessment & Stakeholder Engagement
- Monitoring and analysis of regulatory updates (including laws, guidelines, technical requirements, and trends) issued by relevant regulatory bodies in the territory
- In conjunction with local GRAS SMEs, provide a local assessment/interpretation of new/revised regulatory information and triage for global impact assessment according to company SOPs
- Manage global impact assessments of new/revised regulatory information according to company SOPs
- In conjunction with local PV SMEs, provide a local assessment/interpretation of new/revised PV regulatory intelligence and triage for a global impact assessment according to company SOPs
Regulatory Policy: Intelligence Analysis & Support
- Provide intelligence analyses and support for regulatory policy priorities (e.g., major legislative changes with direct impact on CLIENT)
- Track regulatory policy updates and trends issued by relevant legislative and regulatory bodies
- Provide strategic input to company SMEs by curating impact assessments, including evaluating potential impacts on technical and procedural requirements and translating these into actionable insights
- Support policy activities by providing preliminary analysis of regulatory challenges and opportunities and insights on how to mitigate risks or capitalise on opportunities
- Provide analyses according to company processes and using company templates.
Global-Local Regulatory Alignment & Liaison
- Liaise with local and global GRAS SMEs, clinical, medical affairs, and quality assurance SMEs as required to ensure alignment on impact assessment activities
- Advise internal regulatory teams and GRASP Regional Leads on evolving regulatory expectations
- Ensure alignment between country-specific regulatory intelligence and the company’s global regulatory intelligence/impact assessment framework.
Regulatory Intelligence Infrastructure Management
- Maintain structured regulatory intelligence tracking to ensure timely awareness of emerging regulatory signals
- Contribute to the development and maintenance of regulatory intelligence databases, trackers, and internal communication channels
- Ensure all regulatory intelligence activities adhere to the company’s internal governance policies and compliance standards
- Support the preparation and conduct of pharmacovigilance (PV) inspections and audits, as requested.
Regulatory Expertise
- In-depth understanding of the APAC pharmaceutical regulatory environment, including policy reform trends, approval pathways, and lifecycle management requirements.
Organizational skills
- Exceptional organizational skills to manage multiple tracking systems, prioritize information, and ensure timely delivery of intelligence outputs
- Proven capability to coordinate cross-culturally across time zones and geographic locations, fostering collaboration between global and local teams.
Communication & Stakeholder Management Skills
- Adaptable communication for diverse stakeholders (local and global SMEs)
Excellent English written and verbal communication skills
Experience Level: 5 to 8 years
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