Novo Nordisk

Clinical Operations Lead, Obesity

Novo Nordisk

full-time

Posted on:

Location Type: Office

Location: Søborg • 🇩🇰 Denmark

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Job Level

Senior

About the role

  • Define, set up, and prepare clinical trials with operational excellence
  • Translate strategies and aspirations into operational actions and excellence
  • Assume accountability for the start-up and initiation of one or more global clinical trials
  • Be responsible for trial start-up activities from protocol development to successful patient recruitment
  • Collaborate with cross-functional stakeholders (e.g., Strategic Project Teams, Trial Squads, Medical and Science Teams, Regulatory Affairs) and engage with the external scientific environment

Requirements

  • A MSc in Natural Science and five years of relevant experience, or a BSc in Natural Science or equivalent with at least seven years of relevant experience (e.g. Global Trial Manager, Clinical Research Associate, study nurse)
  • Strong clinical project management experience
  • Knowledge and experience in clinical trial methodology and operational aspects of trial initiation including solid knowledge and experience in clinical IT systems (e.g. EDC, IWRS/RTSM etc.)
  • Excellent planning, communication, coordination, and collaboration skills.
  • Professional proficiency in English.
Benefits
  • Professional development opportunities

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
clinical project managementclinical trial methodologyprotocol developmentpatient recruitmentclinical IT systems
Soft skills
planningcommunicationcoordinationcollaborationaccountability
Certifications
MSc in Natural ScienceBSc in Natural Science