Senior Clinical Trial Manager - Internal Medicine

🔒 Confidential Employer
Posted 7 May 2026
LOCATION
Reading
TYPE
Full-time
LEVEL
Mid-Senior level
CATEGORY
Healthcare
This employer holds a UK Home Office sponsor license — sponsorship for this specific role is at the employer’s discretion

SKILLS

Clinical Trial Management Budget Oversight Monitoring Plan Development CRA Training and Mentoring Study Start-Up Enrollment Management Risk Mitigation Stakeholder Management

FULL DESCRIPTION

Senior Clinical Trial Manager - Internal Medicine

Company: [Employer hidden — sign up to reveal] plc

Location: Sofia, Prague, Budapest, Lisbon, Bucharest, Barcelona, Madrid, Reading (Remote or Office)

Reference: JR144826

Category: Clinical Trial Management

About the role

[Employer hidden — sign up to reveal] plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Trial Manager to join our diverse and dynamic team. As the Senior Clinical Trial Manager, you will hold a crucial role in ensuring the successful delivery of all clinical aspects of the studies. Your expertise and leadership will be instrumental in managing the clinical portion of the budget, developing effective monitoring plans, and driving enrollment to meet project objectives. Moreover, you will liaise with stakeholders, identify and mitigate risks, and provide comprehensive reporting on all clinical activities.

What you will be doing

  • Budget Oversight: Oversee the clinical portion of the budget to ensure efficient resource allocation.
  • Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight.
  • Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
  • Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
  • Improving Study Integrity: Review trip reports and implement corrective and preventative action plans when necessary.
  • Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Your profile

  • A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.
  • Bachelor's degree in health, life sciences, or other relevant fields of study.
  • At least 10+ years of relevant experience in clinical trial management.
  • Preferred: 2+ years of monitoring experience.
  • Experience in managing complex or global trials is advantageous.
  • Preferred: Experience in managing all trial components from start-up to database lock.
  • Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
  • Fluency in English (reading, writing, speaking).

What [Employer hidden — sign up to reveal] can offer you

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, [Employer hidden — sign up to reveal] offers a range of additional benefits.

  • Various annual leave entitlements
  • A range of health insurance offerings
  • Competitive retirement planning offerings
  • Global Employee Assistance Programme
  • Life assurance
  • Flexible country-specific optional benefits

For more details, visit our benefits page.

If you are a current [Employer hidden — sign up to reveal] Employee, please apply here.

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