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Senior Regulatory Affairs Associate (Regional Submission Coordinator)
Primary Location: Serbia, Remote Additional Locations: Croatia, Remote; Poland, Remote; Romania, Remote Job ID R0000040547 Category Regulatory Affairs Date Posted 04/08/2026Overview
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
We are seeking a highly organized and detail-orientedSenior Regulatory Affairs Associateto serve as a Regional Submission Coordinator. This is a key operational role responsible for coordinating all activities required to deliver regulatory submissions across assigned regions, ensuring timely and compliant filings that support our clients' drug development programs.
In this role, you will be at the heart of regulatory submission activities, working collaboratively with global teams, local regulatory representatives, and subject matter experts to ensure successful regulatory outcomes.
Key Responsibilities:
Regional Coordination & Stakeholder Management
Coordinate the preparation, compilation, and submissionof new drug applications and lifecycle management (LCM) activities in alignment with submission strategy as defined by the Regional Regulatory Lead (RRL) and submission team
Coordinate closely with Global Submission Coordinators to ensure completeness of core documentation required to support regional submission planning and requirements
Organize submission team meetingsand facilitate effective communication among all stakeholders including CMC, labelling, RRL, Local Regulatory Representative (LRR), and Regulatory Partner Representative (RPR)
Open required records in submission planning tools and Regulatory Information Management Systems
Prepare Submission Content Plans (SCP)based on country-specific regulatory requirements and prior Health Authority observations to ensure continuous improvement
Coordinate, request, and track documentation from relevant SMEs to ensure timely and complete submission readiness
Provide regular updates to the submission team on status and timelines
M1 Document & Labeling Support
Draft M1 documentsas required and coordinate their review with LRR or RPR
Support labeling preparation, notably in Artwork management system and change control system
Upload M1 documents in archiving system and complete the SCP accordingly
Ensure dispatch of non-eCTD regulatory packages to LRR and RPR
Track dispatched documentation for each country
Ensure submitted documentation is uploaded to archiving system for non-eCTD submissions
Update Veeva as required, including uploading each question received by Health Authorities in a record HAI
Skills & Experience required for the role:
University degreein Life Sciences discipline
3-5 years of experiencein regulatory affairs within the pharmaceutical or biotechnology industry
Regulatory submission strategy and execution experience, ideally global
Strong understanding of regional regulatory submission processes
Experience with different international regulatory submission routespreferred(e.g., ACCESS, reliance pathways)
Excellent project management and organizational skills
Strong communication and stakeholder management abilities
Proficiency in regulatory tracking systems and Microsoft Office Suite
Fluent in English, written and spoken
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