Spécialiste En Réglementation Et Lancement Des Essais Cliniques/ Regulatory & Start-up Specialist

IQVIA

Base: $60,700.00 - $125,200.00; bonus/equity: not ...
Not specified
Site activation activities
Regulatory compliance
Standard operating procedures
IQVIA is seeking a Regulatory & Start-up Specialist to manage site activation activities in compliance with local and international regulations. The role requires at least one year of clinical research experience and involves coordination with various stakeholders to ensure project timelines and quality standards are met

Job Summary

  • Perform tasks at a country level associated with Site Activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
  • Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
  • The potential base pay range for this role, when annualized, is $60,700.00 - $125,200.00.

Matching Summary

Match Score: 75

IQVIA is seeking a Regulatory & Start-up Specialist to manage site activation activities in compliance with local and international regulations. The role requires at least one year of clinical research experience and involves coordination with various stakeholders to ensure project timelines and quality standards are met.

Salary

Base: $60,700.00 - $125,200.00; Bonus/Equity: Not specified; Benefits: Health, wellness, and/or other benefits

Skills & Requirements

Must-have

  • Site Activation activities
  • Regulatory compliance
  • Standard Operating Procedures
  • Project timelines
  • Quality control of documents

Nice-to-have

  • Local expertise
  • Direct contact with sponsors
  • Contingency planning

Key Requirements

  • 1 year clinical research experience
  • Equivalent combination of education, training and experience

Work Rights

Not specified

Tailored Resume

Cover Letter