Contribuyo a la investigación clínica con experiencia y empatía. Y lo hago
Regulatory Affairs Consultant
Primary Location: India, Remote ID de la oferta R0000037354 Categoría Regulatory Affairs Fecha de publicación 03/17/2026Overview
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
Regulatory Affairs Consultant
Around 7-10 years of relevant experience in handling life cycle management (LCM) of approved/marketed drug products (Biologicals, Vaccines, ) in various markets, mainly in US, EU, Japan, Canada Switzerland, Australia.
Good understanding of regulatory framework, including regional trends, for various types of applications and procedures.
Lead and / or contribute to the planning, preparation, authoring and delivery of regulatory maintenance submissions from either a global and/or regional perspective.
Working knowledge of US, EU, Japan, Canada, Switzerland, Australia regulatory procedures including post approval requirements. Knowledge of ROW markets regulatory legislations would be an added advantage
Experience in handling CMC related health authority queries, and author responses to HA requests
Preparation / Review of Regulatory gap analysis and strategy documents (with remediation plans for identified gaps) for submissions like IND, IMPD, DMF, BLA, NDA, and MAA applications.
Authoring and review of CMC component of Marketing Authorization Applications & Variations for various types of medicinal products (orals & parenteral) for filing in EU through different types of procedures (DCP/MRP/National Procedures).
Authoring CMC component for marketed products, of Annual Reports, Variations, expansions, site transfers, Renewals in EU (Type IA/IB/II/IAIN), and US, Canada, Switzerland and RoW markets.
Evaluation of change controls and deviations and identification of required documentation and strategy for US, EU, Japan, Canada, Switzerland, Australia submissions and other markets.
Co-ordination with internal and external stakeholders for documentation required for various submissions. Identify quality and/or timeliness issues with source documents, as early as possible.
Develop up-to-date knowledge about regulatory guideline updates and applying regulatory requirements and their impact on submissions.
Working experience in Regulatory Information Management Systems (RIMS) like Veeva Vault.
Strong communications skills and ability to guide and mentor team members.
Ability to work independently.
Knowledge and Experience:
Several years of experience in an industry-related environment
Education:
Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline, Advanced Degree Preferred
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Perspectivas de los empleados
POR QUÉ TRABAJAR EN PAREXEL
