Global Clinical Research Program Lead

USA-Medtronic MiniMed, Inc 1017; Los Angeles (CA); On-site; USD 109,000 - 185,000; Full time

Benefits offered by this job

Health insurance

401(k) with company match

Job summary

MiniMed is seeking a Clinical Research Program Manager to coordinate and manage clinical activities related to early-stage feasibility studies, collaborating with Program Management, Regulatory Affairs and R&D.

Responsibilities include leading global investigator-sponsored trials, maintaining study timelines, and ensuring regulatory and ethical compliance while resolving program-level issues with cross-functional teams.

Qualifications

• Bachelor’s degree with 5+ years of relevant experience or advanced degree with 3+ years of relevant experience.
• Experience coordinating investigator-sponsored trials and early-stage feasibility studies.
• Ability to operate in a matrixed, cross-functional environment with minimal supervision.

Responsibilities

• Provides clinical program leadership for investigator-sponsored research and feasibility studies.
• Manages a global portfolio of investigator-sponsored research with integrated timelines and deliverables.
• Tracks milestones, communicates risks, and coordinates cross-functional activities with stakeholders.

Skills

Clinical project management

Regulatory affairs liaison

Cross-functional leadership

Study coordination

Education

Bachelor’s degree

Advanced degree

Job description

MiniMed is seeking a Clinical Research Program Manager to coordinate and manage clinical activities related to early-stage feasibility studies, collaborating with Program Management, Regulatory Affairs and R&D.

Responsibilities include leading global investigator-sponsored trials, maintaining study timelines, and ensuring regulatory and ethical compliance while resolving program-level issues with cross-functional teams.