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Intuitive

Clinical Data Manager

Intuitive

Clinical Data Manager at Intuitive managing clinical databases for pre-market and post-market studies. Collaborating with teams to ensure quality and adherence to procedures in the medical device industry.

Posted 7/7/2026full-timeRemote • Sunnyvale • California • 🇺🇸 United StatesMid-LevelSenior💰 $124,900 - $179,700 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing clinical databases for pre-market and post-market studies, with a strong focus on data management plans, EDC design, and adherence to Good Clinical Practices. Proven ability to collaborate with clinical operation teams to ensure high-quality research outcomes.

Highest-signal resume keywords
Data Management ExperienceEDC System ExperienceGood Clinical Practices KnowledgeClinical Trial Process KnowledgeBSc/BA in Scientific or Medical Field

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Database DevelopmentData CleaningData Management PlansStatistical Review SupportQuery Management
Soft Skills
CollaborationProject Support
Tools & Technologies
MedrioMedidata Rave
Industry Keywords
Medical Device IndustryPharmaceutical IndustryClinical ResearchRegulatory Requirements

About the role

Key responsibilities & impact
  • Manage design, development, implementation, validation, maintenance, and support clinical databases related pre-market or post-market clinical studies/registries.
  • Adhere to required departmental operating procedures regarding Data Management for clinical investigations.
  • Collaborate with clinical operation teams, support project goals, and ensure high-quality research and database development.
  • Develop project-specific data management plans, EDC design, create clinical databases, and perform data management.
  • Conduct data cleaning, manage queries, and support statistical reviews.

Requirements

What you’ll need
  • Minimum of 3-5 years of data management experience with a proven track record working in a medical device/pharmaceutical industry.
  • EDC system(s) experience (Preferably Medrio and Medidata Rave)
  • Knowledge of Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology.
  • BSc/BA in a scientific or medical field

Benefits

Comp & perks
  • Health insurance
  • 401(k) matching
  • Paid time off
  • Flexible work arrangements
  • Professional development opportunities