Global Director, Surgical Clinical Development

Bausch + Lomb

Jackson (MS)

On-site

USD 165,000 - 215,000

Full time

13 days ago

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Job summary

Bausch + Lomb, a leading eye health company, seeks a Director of Surgical Clinical Development to shape global clinical strategies for ophthalmic devices from feasibility to post-market studies.

The role partners with R&D, Regulatory, and Quality to drive evidence generation for regulatory submissions and market access in multiple regions. U.S. locations include potential Mississippi operations.

Qualifications

  • Advanced degree in clinical/biomedical science.
  • 7+ years in medical device clinical development.
  • Strong knowledge of GCP and ISO 14155.
  • Experience with global regulatory submissions (FDA/EU/PMDA).
  • Experience in ophthalmic surgery or related field.

Responsibilities

  • Lead global clinical development strategy for surgical device programs from early-stage through post-market.
  • Oversee regulatory submissions ensuring alignment with FDA, EU MDR/CE, China NMPA and PMDA pathways.
  • Design and oversee clinical trials including pivotal and post-approval studies across markets.
  • Develop and author regulatory and clinical documents (investigation plans, protocols, reports, submission dossiers).
  • Collaborate cross-functionally with R&D, Regulatory, Quality, and Commercial to translate insights into product development and go-to-market strategies.
  • Manage budgets and resources; ensure timely data submissions to regulators.
  • Cultivate relationships with investigators, KOLs, and regulatory experts in surgical ophthalmology.

Skills

Leadership
Strategic thinking
Project management
Communication
Team collaboration

Education

MD/DO/PhD or equivalent

Job description

Bausch + Lomb, a leading eye health company, seeks a Director of Surgical Clinical Development to shape global clinical strategies for ophthalmic devices from feasibility to post-market studies.

The role partners with R&D, Regulatory, and Quality to drive evidence generation for regulatory submissions and market access in multiple regions. U.S. locations include potential Mississippi operations.

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