Fsp Study Start-up Manager

IQVIA UK

Base: $74,600.00 - $216,000.00 annualized; bonus/e...
Not specified
7 years relevant experience in scientific or clinical environment
Strong negotiation and communication skills
Thorough understanding of gcp and ich guidelines
IQVIA UK is seeking a Study Start-up Manager to oversee site activation and regulatory activities for clinical trials. The ideal candidate will have a strong background in clinical research, excellent communication skills, and a thorough understanding of regulatory requirements

Job Summary

  • The role involves directing and managing the delivery of site activation, maintenance, and regulatory activities for selected studies or multi-protocol programs.
  • Candidates must provide specialist regulatory and technical scientific support to facilitate efficient business development and study initiation while ensuring compliance.
  • IQVIA offers a competitive base pay range from $74,600.00 to $216,000.00 annually along with potential incentive plans and comprehensive benefits.

Matching Summary

Match Score: 85

IQVIA UK is seeking a Study Start-up Manager to oversee site activation and regulatory activities for clinical trials. The ideal candidate will have a strong background in clinical research, excellent communication skills, and a thorough understanding of regulatory requirements.

Salary

Base: $74,600.00 - $216,000.00 annualized; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • 7 years relevant experience in scientific or clinical environment
  • Strong negotiation and communication skills
  • Thorough understanding of GCP and ICH guidelines
  • Experience with CTMS and project planning systems
  • Ability to work through others on complex projects

Nice-to-have

  • Proven ability to establish long-standing customer relationships
  • Experience delivering presentations to clients and professional bodies
  • Strong leadership skills to motivate and mentor colleagues
  • Ability to exercise independent judgment taking calculated risks

Key Requirements

  • Bachelor's Degree in Life sciences or related field
  • 7 years' relevant experience in international scientific or clinical environment
  • Demonstrated proficiency in using systems and technology
  • Good regulatory and/or technical writing skills

Work Rights

Not specified

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