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Haleon

Senior Clinical Study Manager

Haleon

Senior Clinical Study Manager leading clinical study teams for Haleon’s health products. Planning, executing, and overseeing clinical trials while ensuring compliance with regulations and quality standards.

Posted 7/14/2026full-timeWeybridge • 🇬🇧 United KingdomSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in study operational strategy, ensuring compliance with ICH/GCP and local regulations while providing leadership in the execution of clinical trials. Proven ability to manage relationships with clinical sites, CROs, and vendors to deliver successful trial outcomes.

Highest-signal resume keywords
Study Operational StrategyClinical Trial ManagementICH/GCP ComplianceProject Management ExperienceOperational Support

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical ResearchStudy DesignProtocol DevelopmentTrial ExecutionData Tracking
Soft Skills
LeadershipCommunicationCollaboration
Industry Keywords
CRO ManagementVendor OversightGlobal Scientific FunctionsMedical FunctionsOperational Specialty Training

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Exhibits strong study operational strategy to plan and oversee execution of assigned studies
  • Acts as Study Team Leader and primary operational contact for 1–3 trials of average design and protocol complexity
  • Responsible for the implementation, conduct and tracking of study trials in compliance with ICH/GCP and local regulations
  • Provides operational and strategic leadership to assure successful delivery of trials
  • Provides oversight of clinical sites, CROs and vendor activities
  • Leads or participates in clinical site assessments
  • Contributes to plans and study documents from an operational standpoint

Requirements

What you’ll need
  • Bachelor’s degree
  • 5 or more years of industry project management experience
  • Relevant clinical research or operational specialty training preferred
  • Experience providing operational support across global scientific and medical functions
  • Externally facing role experience and technical expertise

Benefits

Comp & perks
  • Health insurance
  • 401(k) matching
  • Flexible working hours
  • Paid time off
  • Professional development opportunities