Clinical Study Manager I

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,Meeting with clients as needed throughout study, and organizing study logistics and personnel.In addition, you will be present at critical events and dosings 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.

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 requiredShown ability to handle multiple prioritiesExcellent oral and written communication skillsAbility to work without close supervisionAbility to work flexible hours required for study conductYou will utilize customer service skillsClinical Research experience preferredCelerion Values: Integrity Trust Teamwork Respect Are you ready to join our team? Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability. Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.