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Kerr Dental

SSO Clinical Project Manager

Kerr Dental

CPM responsible for planning, executing, and reporting on assigned Global Drug Development studies. Ensures compliance with Novartis processes and regulatory requirements during trial execution.

Posted 5/13/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $145,600 - $270,400 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • The CPM is accountable for the day-to-day planning, executing and reporting of assigned Global Drug Development studies
  • Responsible for assuring aligned communication with Trial Lead and other CTT members
  • Supports SSO Study Start-up Managers in the development of country/cluster/hub study execution plans
  • Proactively identifies risk and opportunities for the assigned studies within the country/cluster/hub
  • Maintains a strong knowledge of the study protocol to answer standard operational questions from CRAs and site personnel
  • Drives the conduct of the study, tracks status, maintains relevant reporting systems, oversees forecasts, progress, and mitigation plans
  • Ensures recruitment targets are met and reviews enrollment at the site level
  • Oversees local study team activities to achieve study timelines and quality execution
  • Conducts or coordinates training, as needed, for CRAs to support site readiness to recruit and study execution
  • Accountable for monitoring quality and issue resolution through timely review and approval of study monitoring visit reports

Requirements

What you’ll need
  • A minimum of a bachelor's degree in scientific or health discipline
  • Fluent in both written and spoken English
  • Minimum 5 years’ experience in clinical research overseeing (project management) and/or monitoring clinical trials
  • Capable of leading in a matrix environment, without direct reports and working cross-borders managing global studies in various countries
  • Understanding of all aspects of clinical drug development with particular emphasis on monitoring and study execution
  • Strong project management capabilities with demonstrated ability to problem solve and mediate complex issues
  • Thorough understanding of the international aspects of drug development process, including strong knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities regulations and Novartis standards
  • Demonstrated negotiation and conflict resolution skills both internally and externally (site relationships)

Benefits

Comp & perks
  • Health insurance
  • Life and disability benefits
  • 401(k) with company contribution and match
  • Generous time off package including vacation, personal days, holidays and other leaves
  • Performance-based cash incentive
  • Eligibility for annual equity awards

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical researchproject managementmonitoring clinical trialsstudy executionrisk identificationreporting systemsenrollment reviewtraining coordinationissue resolutionprotocol knowledge
Soft Skills
communicationleadershipproblem solvingnegotiationconflict resolutioncross-border collaborationmatrix managementteam oversightadaptabilityinterpersonal skills
Certifications
bachelor's degree in scientific disciplinebachelor's degree in health discipline