Global Senior Manager, Clinical Science (Remote)

Leica Biosystems; Vista (CA); Remote; USD 170,000 - 190,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

401(k) plan

Paid time off

Job summary

Leica Biosystems, a Danaher operating company, is seeking a Sr. Manager, Clinical Science (Global - Remote) to lead clinical trial strategies across US and EU markets.

You will manage a team of clinical scientists, shape study designs, ensure regulatory compliance, and drive milestones for pivotal digital pathology studies. Collaborating with Regulatory Affairs, R&D, Medical Affairs, and CROs, you will integrate clinical insights into product development, support submissions, and disseminate

Qualifications

• Bachelor’s degree in Life Sciences with 12+ years in clinical research or Master/Doctoral with 10+ years.
• 4+ years direct leadership experience managing clinical scientists.
• Deep understanding of clinical study design in diagnostics/medical device/pharma.
• Ability to review complex trial data and guide study protocols.

Responsibilities

• Oversee clinical study planning and design for Digital Pathology, IHC/ISH, CDx and Medical Device.
• Ensure rigor of protocols, CRFs, study reports and other docs.
• Lead cross-functional collaboration with R&D, Regulatory, Medical Affairs and CROs.
• Support regulatory submissions with scientific data interpretation.
• Build and mentor a high-performing team of clinical scientists.
• Maintain relationships with internal teams and external partners to ensure program success.
• Analyze data, contribute to submissions, and disseminate findings through publications.

Skills

Leadership

Regulatory communication

Cross-functional collaboration

Clinical study leadership

Scientific interpretation

Strategic thinking

Education

Bachelor’s in Life Sciences

Master/Doctoral in related field

Job description

Leica Biosystems, a Danaher operating company, is seeking a Sr. Manager, Clinical Science (Global - Remote) to lead clinical trial strategies across US and EU markets.

You will manage a team of clinical scientists, shape study designs, ensure regulatory compliance, and drive milestones for pivotal digital pathology studies. Collaborating with Regulatory Affairs, R&D, Medical Affairs, and CROs, you will integrate clinical insights into product development, support submissions, and disseminate