Regulatory Affairs - Talent Pool
Poland, Remote Additional Locations Croatia-Remote; Croatia-Zagreb; Hungary-Budapest; Hungary-Remote; Poland-Warsaw-Business Garden; Romania-Bucharest-Metropolis Center; Romania-Remote; Serbia-Belgrade; Serbia-Remote ID de la oferta R0000032994 Categoría Consulting Fecha de publicación 04/15/2025Overview
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
Join Parexel's Regulatory Affairs Team: Shape the Future of Healthcare
Parexel, a leading Clinical Research Organization, is seeking talented professionals at all levels to join our dynamic Regulatory Affairs and Operations team. We are looking for Associates, Consultants, and Senior Experts who are passionate about ensuring regulatory success in the ever-evolving pharmaceutical and biotechnology landscape.
Who We Are:At Parexel, our Regulatory Affairs team is at the forefront of global healthcare innovation. We work closely with health authorities worldwide, including the US-FDA, EMA, and NMPA, to develop unique regulatory strategies, secure submission approvals, and maintain compliance for trials and products across diverse therapeutic areas.
What We Offer:
Exposure to cutting-edge projects in Orphan Drug, Rare Disease, OTC Drug, Cell and Gene Therapies (C>), and more
Opportunity to work with global teams and clients
Career growth across various levels from Associate to Senior Consultant
Continuous learning and development in a rapidly evolving field
Possibility to work from home
Key Responsibilities Across Levels:
Ensure regulatory submissions and activities adhere to global health authority guidelines
Develop and execute regulatory strategies
Collaborate with cross-functional teams to drive project success
Maintain client relationships and deliver high-quality consultancy services
Stay updated on regulatory trends and contribute to process improvements
Requirements:
University-level education in Life Sciences
Previous experience in regulatory affairs (level-dependent)
Strong team spirit, flexibility, accountability, and organizational skills
Fluency in English (written and spoken)
Desire to grow in a fast-paced, innovative environment
Register your interest at Parexel and be part of a team that's shaping the future of healthcare through regulatory excellence. Whether you are starting your career or bringing years of expertise, we hope we can find a place for you to thrive and make a difference.
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POR QUÉ TRABAJAR EN PAREXEL
