Senior Manager Clinical Affairs

Added
8 days ago
Type
Full time
Salary
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Related skills

gcp regulatory affairs clinical trials clinical study management iso 14155

πŸ“‹ Description

  • Play a key role in the development of company's strategy for clinical studies to meet business
  • Acting as a key strategic partner to Regulatory Affairs to support regulatory approval of new
  • Responsible for managing resource and study budget to ensure clinical studies are conduced on
  • Build strong and sustaining relationship with investigational sites and investigators for ongoing
  • Work closely with data management to provide guidance on development of case report form (CRF)
  • Work closely with Biostats in study design, developing statistical analysis plan (SAP), analysis

🎯 Requirements

  • Minimum Education: Bachelor's or Master's degree in scientific field/MD/ PhD with minimum 12 years
  • Minimum of 5 years of experience independently managing clinical studies through different study
  • Excellent clinical operation and project management skills, with strong experience collaborating or
  • Proven track record of strong cross-functional and key opinion leader management
  • Strong experience with clinical study resource and budget management
  • Strong experience supporting development of scientific and regulatory strategy for clinical studies

🎁 Benefits

  • Market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity
  • Equal Opportunity Employer
  • Preference given to qualified candidates who do not reside in certain states (Alabama, Arkansas
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