I contribute to clinical research with expertise and empathy. And I do it
Regulatory Affairs Consultant Safety & Labelling (home or office based)
Primary Location: Romania, Bucharest Additional Locations: Croatia, Remote; Croatia, Zagreb; Czech Republic, Prague; Czech Republic, Remote; Hungary, Budapest; Hungary, Remote; Poland, Remote; Poland, Warsaw; Romania, Remote; Serbia, Belgrade; Serbia, Remote Job ID R0000037590 Category Regulatory Affairs Date Posted 12/18/2025Overview
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 an experienced Regulatory Affairs Consultant Safety & Labelling to develop and execute artwork strategies for our global product portfolio. In this critical role, you will ensure comprehensive oversight throughout the product lifecycle while serving as the primary liaison between Regulatory Affairs and various stakeholders.
The role can be home or office based in various European locations.
Role Responsibilities:
Conduct and deliver high quality, on time safety labelling regulatory activities, including compliant management of all internal tools and client systems;
Author administrative and regulatory documents/deliverables and collaborate with project SMEs and client stakeholders to prepare submission packages;
Full management of safety labelling submissions (i.e. planning, submission package compilation, RIMS maintenance, RtQ preparation, Spontaneous HA queries, etc.);
Act as main GRA point of contact for local regulatory and other stakeholders
Tracking and management of all EU Product Information, alignment with QRD requirements and ability to manage EU linguistic review, readability testing and translation activities.
Supporting regulatory inputs into Periodic Safety Update Reports (PSUR) and potential impact on labelling
Participation in change control process for safety labelling update
Skills and Experience required for the role:
Bachelor's Degree in a Scientific or Technical Discipline
Knowledge of EU regulatory requirements for medicinal product labelling
Familiarity with the Company Core Datasheet (CCDS) and its implementation into labelling and artworks
Understanding of Safety Signal Management and the impact of confirmed safety signals on labelling
Excellent communication and stakeholder management skills;
Strong organizational and time management skills;
Strong problem-solving skills;
Coordinate all assigned activities;
‘Proactive’ and ‘efficient' work ethic;
Strong oral and written communication skills, with proven ability to work efficiently as part of a team;
Strong interpersonal skills;
Fluent in English, written and spoken
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