Celerion

Clinical Study Manager I

Celerion

full-time

Posted on:

Location Type: Office

Location: Tempe • Arizona • 🇺🇸 United States

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Job Level

Mid-LevelSenior

About the role

  • Overall management and oversight of assigned Clinical Studies.
  • Ensure on-time performance with defect-free execution of studies working with support divisions (recruiting, data management, statistics).
  • Organize study initiation meetings to plan execution.
  • Facilitate study review meetings for pre-study, in-process and post-study review.
  • Problem solve during study conduct and be present at critical events and dosing.
  • Meet with clients throughout study and build client relationships.
  • Organize study logistics and personnel.
  • Craft and edit reports and respond to client issues, concerns and requests.
  • Adhere to milestone guidelines and ensure profitability through budgeting and expense control.

Requirements

  • Bachelor’s degree in a related discipline required.
  • Clinical Trial experience may be considered in lieu of degree in some situations.
  • Industry experience and knowledge of medical terminology preferred.
  • Demonstrated organizational, time management and multi-tasking skills required.
  • Shown ability to handle multiple priorities.
  • Excellent oral and written communication skills.
  • Ability to work without close supervision.
  • Ability to work flexible hours required for study conduct.
  • Customer service skills.
  • Clinical Research experience preferred.

Applicant Tracking System Keywords

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

Hard skills
Clinical Trial experienceClinical Research experienceBudgetingExpense controlReport craftingData managementStatistics
Soft skills
Organizational skillsTime managementMulti-taskingProblem solvingClient relationship buildingOral communicationWritten communicationAbility to work independentlyFlexibility
Certifications
Bachelor’s degree