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Parexel

Senior Manager, Regulatory Affairs

Parexel

Senior Manager in Regulatory Affairs at Parexel leading teams and providing regulatory guidance for clinical trials. Extensive experience in EU Clinical Trials Regulation (EU CTR) and client consultancy.

Posted 7/24/2026full-timeRemote • 🇮🇳 IndiaSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in EU Clinical Trials Regulation (EU CTR) and extensive experience in Regulatory Affairs, with a strong focus on team leadership, stakeholder management, and delivering client-focused regulatory consultancy.

Highest-signal resume keywords
EU Clinical Trials Regulation (EU CTR)Regulatory Affairs ExpertiseTeam LeadershipStakeholder ManagementAnalytical Problem-Solving

ATS Keywords

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Applicant Tracking System Keywords

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Soft Skills
CoachingMentoringCommunication
Industry Keywords
Regulatory AuditsRegulatory InspectionsConsultancy

About the role

Key responsibilities & impact
  • Provide leadership and direction to consultants, senior consultants and managers
  • Act as the Subject Matter Expert (SME) for EU Clinical Trials Regulation (EU CTR)
  • Drive capability building through coaching and mentoring
  • Support regulatory audits and inspections
  • Deliver regulatory consultancy and client-focused guidance

Requirements

What you’ll need
  • Extensive experience in Regulatory Affairs
  • Expertise in EU Clinical Trials Regulation (EU CTR)
  • Experience leading and developing teams
  • Strong analytical and problem-solving skills
  • Must have excellent stakeholder management and communication skills

Benefits

Comp & perks
  • Health insurance
  • Professional development opportunities