Sr. Clinical Research Specialist, (clinical Operations Start-up)

J&J FAMILY OF COMPANIES

Irvine, California, United States of America
Base: $92,000.00 - $148,350.00; bonus/equity: not ...
Hybrid
Bachelor's degree in life science or related field
Minimum 4 years clinical research experience
Knowledge of ich-gcp and fda regulations
The Senior Clinical Research Specialist will oversee the execution of clinical trials for Johnson & Johnson MedTech Electrophysiology while ensuring compliance with global regulations

Job Summary

  • The Senior Clinical Research Specialist will oversee the execution of clinical trials for Johnson & Johnson MedTech Electrophysiology while ensuring compliance with global regulations.
  • This role involves managing site relationships, developing study documents, and overseeing Clinical Research Associates to deliver projects on time and within budget.
  • Employees are eligible for comprehensive benefits including 120 hours of vacation, 13 days of holiday pay, and up to 480 hours of parental leave.

Matching Summary

The Senior Clinical Research Specialist will oversee the execution of clinical trials for Johnson & Johnson MedTech Electrophysiology while ensuring compliance with global regulations.

Salary

Base: $92,000.00 - $148,350.00; Bonus/Equity: Not specified; Benefits: 120 hours vacation, 13 days holiday, 480 hours parental leave

Skills & Requirements

Must-have

  • Bachelor's degree in Life Science or related field
  • Minimum 4 years clinical research experience
  • Knowledge of ICH-GCP and FDA regulations
  • Experience with medical device trials
  • Site management and feasibility assessment skills

Nice-to-have

  • Mentoring team members and junior staff
  • Strong presentation and technical writing skills
  • Collaborative relationship building with stakeholders
  • Experience with post-market clinical follow-up plans
  • Leadership in cross-functional project delivery

Key Requirements

  • BS with at least 4 years relevant experience
  • MS with at least 3 years relevant experience
  • PhD with at least 2 years relevant experience
  • Medical device industry experience highly preferred
  • Certifications like CCRA, GCP, or ISO 14155 preferred

Work Rights

Not specified

Tailored Resume

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