Clinical Project Manager (m/f/d)

Johnson & Johnson MedTech

Aachen, North Rhine-Westphalia, Germany
Base: 75.000 eur to 118.450 eur; bonus/equity: ann...
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Gcp and regulatory compliance expertise
Eu regulatory submissions experience
German and english language proficiency
** Johnson & Johnson MedTech is seeking a Clinical Project Manager in Aachen, Germany, to lead the operational activities of clinical studies across the EU/EMEA region. The ideal candidate should possess significant experience in clinical research, particularly within the medical device industry, and demonstrate strong project management skills. **

Job Summary

  • The Clinical Project Manager Europe is responsible for managing the operational activities of assigned clinical studies across the EU/EMEA region, ensuring compliance with GCP/ICH guidelines and regulations.
  • Key responsibilities include leading comprehensive study management, overseeing documentation development, ensuring compliance with SOPs and regulatory requirements, and managing project timelines and risks.
  • The company offers a comprehensive benefits package including an annual bonus, vacation days, parental leave, well-being reimbursement, and various insurance plans.

Matching Summary

Match Score: 75

** Johnson & Johnson MedTech is seeking a Clinical Project Manager in Aachen, Germany, to lead the operational activities of clinical studies across the EU/EMEA region. The ideal candidate should possess significant experience in clinical research, particularly within the medical device industry, and demonstrate strong project management skills. **

Salary

Base: 75.000 EUR to 118.450 EUR; Bonus/Equity: annual bonus; Benefits: vacation days, parental leave, well-being reimbursement, insurance plans

Skills & Requirements

Must-have

  • GCP and regulatory compliance expertise
  • EU regulatory submissions experience
  • German and English language proficiency
  • Cross-functional team collaboration
  • Clinical study management

Nice-to-have

  • High attention to detail
  • Ability to work in fast-paced environments
  • Strong prioritization and organizational skills

Key Requirements

  • Bachelor's degree in a medical/scientific field
  • Minimum 5 years clinical research experience
  • Minimum 2 years medical device industry leadership/project management
  • Experience with pre- and post-market clinical strategies
  • PMP or CCRP certification preferred

Work Rights

Not specified

Tailored Resume

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