Contribuyo a la investigación clínica con experiencia y empatía. Y lo hago
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 ID de la oferta R0000037590 Categoría Regulatory Affairs Fecha de publicación 12/18/2025Overview
Como parte de Consultoría de Parexel, cumplirá un rol vital al asistir a las empresas biofarmacéuticas y de dispositivos médicos a transitar el complejo y siempre cambiante entorno regulatorio. Respaldado por su experiencia científica, técnica y regulatoria, trabajará de cerca con los clientes para desarrollar e implementar estrategias regulatorias que colocarán sus medicamentos en el mercado con mayor rapidez y los mantendrán allí.
Valoramos la colaboración, la innovación y el aprendizaje continuo. Como miembro de nuestro equipo, se asociará con un grupo diverso de clientes y estará expuesto a diversos tipos de medicamentos y áreas terapéuticas. Asimismo, desarrollará sus habilidades a través de asignaciones desafiantes y con la mentoría de profesionales experimentados en asuntos regulatorios. Además, disfrutará de la flexibilidad de trabajar en modalidad remota, al tiempo que forma parte de un equipo colaborador y dinámico.
Perfil del éxito
¿Posee estas competencias sociales y rasgos interpersonales para tener éxito en Parexel?
- Comunicador
- Estratégico
- Constructor de relaciones
- Solucionador de problemas
- Orientado al detalle
- Impulsado por los resultados
Acerca de este rol
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
Perspectivas de los empleados
POR QUÉ TRABAJAR EN PAREXEL
