Celerion
4111.4200 - Clinic
ClinicalStudyManager
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Study Manager at Celerion. Skills: study management, client relationships, reporting. Oversight and conduct of clinical studies. Ensure compliance, quality, and profitability of clinical studies”
What You'll Achieve.
On-time performance with defect-free execution of each study; ensure profitability through budgeting and expense control
Industry & Context.
Problem solving as needed during study conduct
plan to work some evening and weekends, present at critical events and dosing of a study
What They're Looking For.
Must Have
Bachelor’s degree in a related discipline required, 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, You will utilize customer service skills
Nice to Have
Clinical Trial experience may be considered in lieu of degree in some situations, Industry experience and knowledge of medical terminology preferred, Clinical Research experience preferred
What You'll Do.
Oversight and conduct of clinical studies
and profitability of clinical studies
Respond to internal and external client issues
Plan execution of study
Facilitate study review meetings
Problem solving as needed during study conduct
Organize study logistics and personnel
Build client relationships that result in additional business
Craft and edit reports
Adhere to milestone guidelines
Ensure profitability through budgeting and expense control
How You'll Work.
Team & Collaboration
working with support divisions to ensure timelines are being met
Communication Scope
Excellent oral and written communication skills
Process & Methodology
process management, cross-functional coordination, vendor/stakeholder management, resource planning
Full Job Description
## Description Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. As a Clinical Study Manager you are responsible for oversight and conduct of clinical studies. You will ensure compliance, quality, and profitability of clinical studies. You respond to internal and external client issues, concerns, and requests by applying study management techniques and tools. In this role you should plan to work some evening and weekends. Primary Responsibilities: You are responsible for the overall management of assigned Clinical Studies to include: · On-time performance with defect-free execution of each study, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), · Organizing study initiation meetings to plan execution of study, · Facilitating study review meetings for pre-study, in-process and post study review, · Problem solving as needed during study conduct, · Meeting with clients as needed throughout study, and organizing study logistics and personnel. · In addition, you will be present at critical events and dosing of a study. You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability through budgeting and expense control on a total and individual study basis. ## Primary Responsibilities On-time performance with defect-free execution of each study, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), Organizing study initiation meetings to plan execution of study, Facilitating study review meetings for pre-study, in-Problem solving as needed during study conduct
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