Senior Manager, Regulatory Affairs

Posted:
7/23/2026, 11:36:27 PM

Location(s):
Karnataka, India ⋅ Maharashtra, India ⋅ Mumbai, Maharashtra, India ⋅ Bengaluru, Karnataka, India

Experience Level(s):
Senior

Field(s):
Legal & Compliance

Workplace Type:
Remote

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.

Parexel

Website: https://www.parexel.com/

Headquarter Location: Waltham, Massachusetts, United States

Employee Count: 10001+

Year Founded: 1982

IPO Status: Delisted

Last Funding Type: Venture - Series Unknown

Industries: Biopharma ⋅ Biotechnology ⋅ Consulting ⋅ Industrial ⋅ Medical Device ⋅ Web Development

Visa Sponsorship: Sponsors work visas