Clinical Development Lead

Roche

Tucson, AZ, US
Base: $100,500-$186,700; bonus/equity: discretiona...
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Doctoral or advanced degree in life sciences
5+ years scientific research experience
Proven scientific writing experience
** Roche is seeking a Clinical Development Lead in Tucson, AZ, to support clinical evidence generation and study design for In Vitro Diagnostics (IVD). The ideal candidate will have a doctoral degree and substantial experience in scientific writing and regulatory documentation, particularly in IVD or medical devices. **

Job Summary

  • The Clinical Development Lead serves as a strategic partner within the Clinical Development team to support clinical evidence generation and study design for In Vitro Diagnostics.
  • This role involves designing scientifically sound clinical studies, conducting comprehensive literature reviews, and providing medical input for regulatory submissions.
  • Roche offers a culture that encourages personal expression, open dialogue, and genuine connections where every voice matters.

Matching Summary

Match Score: 75

** Roche is seeking a Clinical Development Lead in Tucson, AZ, to support clinical evidence generation and study design for In Vitro Diagnostics (IVD). The ideal candidate will have a doctoral degree and substantial experience in scientific writing and regulatory documentation, particularly in IVD or medical devices. **

Salary

Base: $100,500-$186,700; Bonus/Equity: Discretionary annual bonus available; Benefits: Standard benefits package detailed at provided link

Skills & Requirements

Must-have

  • Doctoral or advanced degree in life sciences
  • 5+ years scientific research experience
  • Proven scientific writing experience
  • Experience with clinical study protocols
  • Knowledge of IVDR performance evaluation

Nice-to-have

  • Experience with regulatory writing for IVD
  • Understanding of laboratory techniques like PCR
  • Ability to travel up to 25%
  • Mentoring less experienced team members
  • Agility and effective decision-making skills

Key Requirements

  • PhD, MD, PharmD or equivalent doctoral degree
  • 5+ years of scientific research and writing experience
  • Experience with regulatory documents for IVD or medical devices

Work Rights

Not specified

Tailored Resume

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