Site Activation Manager

IQVIA

Base: $74,600.00 - $216,000.00; bonus/equity: ince...
Site activation and maintenance management
Regulatory strategy and compliance
Clinical trial project oversight
Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources

Job Summary

  • Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.
  • Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
  • IQVIA is proud to be an equal opportunity employer and is committed to integrity in the hiring process with a zero tolerance policy for candidate fraud.

Matching Summary

Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources.

Salary

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

Skills & Requirements

Must-have

  • Site activation and maintenance management
  • Regulatory strategy and compliance
  • Clinical trial project oversight
  • Cross-regional collaboration
  • Clinical trial management systems (CTMS)
  • Budget and resource oversight
  • GCP and ICH guidelines application

Nice-to-have

  • Mentoring and coaching skills
  • Strong negotiation and communication
  • Presentation and training delivery
  • Multi-protocol program management
  • Quality management collaboration
  • Regulatory intelligence analysis

Key Requirements

  • Bachelor's Degree in Life Sciences or related field
  • 7 years relevant scientific or clinical experience
  • Experience in an international role
  • Knowledge of regulated clinical trial environment
  • Proficiency with clinical trial systems and technology
  • Strong leadership and organizational skills
  • Excellent understanding of study financial management

Work Rights

Not specified

Tailored Resume

Cover Letter