Hybrid Clinical Research Program Manager, Early-Stage Trials

MiniMed Group

California

Hybrid

USD 121,000 - 205,000

Full time

3 days ago
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Benefits offered by this job

Competitive salary
Flexible benefits
Hybrid work

Job summary

MiniMed is seeking a Clinical Research Program Manager in Northridge, CA. This hybrid role leads investigator-sponsored and early-stage feasibility studies, coordinating across PM, Regulatory, and R&D teams to ensure on-time delivery.

The role requires a Bachelor's with 5+ years of relevant experience (or advanced degree with 3+ years) and experience in investigator-sponsored trials within a matrixed environment.

Qualifications

  • Bachelor’s degree with 5+ years of relevant experience; or advanced degree with 3+ years of relevant experience.
  • Experience working in investigator-sponsored clinical trials.
  • Experience in a matrixed, cross-functional environment.

Responsibilities

  • Provides clinical program leadership for investigator-sponsored research and early-stage feasibility studies.
  • Manages a global portfolio of investigator-sponsored research with integrated timelines and deliverables.
  • Tracks milestones and communicates risks and resolutions to stakeholders.
  • Partners with sponsors and cross-functional teams to support scientifically valid studies.
  • Coordinates cross-functional clinical research activities and aligns execution with program plans.
  • Represents MiniMed in discussions with investigators and authorities.
  • Builds relationships with sponsors, sites, PM, Clinical Affairs, Regulatory Affairs and R&D.

Skills

Clinical research
Project management
Cross-functional coordination
Regulatory knowledge

Education

Bachelor's degree
Advanced degree

Job description

MiniMed is seeking a Clinical Research Program Manager in Northridge, CA. This hybrid role leads investigator-sponsored and early-stage feasibility studies, coordinating across PM, Regulatory, and R&D teams to ensure on-time delivery.

The role requires a Bachelor's with 5+ years of relevant experience (or advanced degree with 3+ years) and experience in investigator-sponsored trials within a matrixed environment.

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