Chef Principal Des Essais Cliniques, Iqvia Biotech/senior Clinical Trial Manager, Iqvia Biotech

IQVIA UK

Base: $116,300.00 - $193,800.00 annualized; bonus/...
Not specified (potentially hybrid or flexible)
5 years clinical research experience
Oncology therapeutic area expertise
Good clinical practice (gcp) knowledge
IQVIA Biotech is seeking a Senior Clinical Trial Manager with a focus on oncology, responsible for leading clinical trials to accelerate patient access to innovative treatments. The role requires collaboration with clinical teams and stakeholders, ensuring compliance with regulatory standards and effective risk management

Job Summary

  • The role involves exclusively collaborating with biotechnology and emerging biopharmaceutical companies to accelerate patient access to innovative treatments.
  • Candidates must ensure clinical trials meet regulatory requirements including ICH-GCP guidelines while managing project risks and quality standards.
  • The position requires leading clinical teams, managing recruitment targets, and overseeing the financial aspects of project funding including Estimate at Completion.

Matching Summary

Match Score: 85

IQVIA Biotech is seeking a Senior Clinical Trial Manager with a focus on oncology, responsible for leading clinical trials to accelerate patient access to innovative treatments. The role requires collaboration with clinical teams and stakeholders, ensuring compliance with regulatory standards and effective risk management.

Salary

Base: $116,300.00 - $193,800.00 annualized; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Health, wellness, and other benefits included

Skills & Requirements

Must-have

  • 5 years clinical research experience
  • Oncology therapeutic area expertise
  • Good Clinical Practice (GCP) knowledge
  • ICH guideline compliance
  • Project recruitment strategy execution
  • Clinical risk management planning
  • Budget and EAC financial oversight

Nice-to-have

  • Global trial perspective
  • Proposal development participation
  • Mentoring new colleagues
  • Site visit support capability
  • Agile collaborative culture fit
  • International stakeholder management

Key Requirements

  • Bachelor's degree in health sciences or scientific discipline
  • Minimum 5 years experience in clinical research or monitoring
  • Sound knowledge of GCP and ICH guidelines
  • In-depth understanding of protocols and therapeutic aspects
  • Understanding of project financial aspects

Work Rights

Not specified

Tailored Resume

Cover Letter