Hiring.Camp

Senior Manager, Regulatory Affairs

Parexel

·

2 days ago

Location
India-Bengaluru-Remote · India-Mumbai-Remote
Workplace
Remote
Type
Full-time
Department
Legal
Seniority
Senior
Source
Workday

Description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

A Senior Manager within R&A provides leadership and direction to consultants, senior consultants and managers, actively managing employee performance and development. A Senior Manager acts as a role model and provides a broad range of consulting services and may be responsible for a specific function/technical area.

Key Responsibilities

  • Extensive experience in Regulatory Affairs, including expertise in EU Clinical Trials Regulation (EU CTR) and experience leading and developing teams.
  • Act as the Subject Matter Expert (SME) for the EU Clinical Trials Regulation (EU CTR), providing strategic regulatory guidance and ensuring compliant implementation.
  • Drive capability building within the team through coaching, mentoring, training, and knowledge-sharing initiatives.
  • Contribute to organizational EU CTR-related projects, process improvements, and strategic initiatives.
  • Support the development, review, and maintenance of functional Standard Operating Procedures (SOPs).
  • Provide support during regulatory audits and inspections.
  • Deliver regulatory consultancy and client-focused guidance, fostering strong stakeholder partnerships.
  • Lead and manage a team, ensuring performance, development, and operational excellence.

Skills and Competencies

  • Strong expertise in EU Clinical Trials Regulation (EU CTR) and associated regulatory requirements.
  • Ability to interpret regulatory intelligence, assess impact, and translate requirements into practical processes and implementation plans.
  • Solid understanding of regulatory operations, workflows, and compliance standards.
  • Excellent stakeholder management and communication skills, with experience collaborating across global teams and clients.
  • Strong analytical, problem-solving, decision-making, and risk mitigation capabilities in a dynamic environment.
  • Demonstrated ability to work collaboratively and influence cross-functional teams in a consultative manner.

Skills

Clinical TrialsCompliance

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Remote Senior Manager, Regulatory Affairs at Parexel | Hiring.Camp