Clinical Study Manager I

Celerion; Tempe (AZ); On-site; USD 90,000 - 120,000; Full time

Job summary

Celerion is seeking a Clinical Study Manager to oversee the conduct and integrity of clinical studies, ensuring quality, compliance, and profitability. The role requires coordinating with support divisions to meet timelines, organizing initiation and review meetings, and addressing client requests with proactive problem solving.

Some evenings and weekends may be required. Primary responsibilities include budgeting, milestone adherence, and building strong client relationships to drive additional

Responsibilities

• On-time performance with defect-free execution of each study, working with support divisions to ensure timelines are met in clinical studies (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 during study conduct.
• Meeting with clients and organizing study logistics and personnel.
• Build client relationships to generate additional business, edit reports, respond to client issues, adhere to milestone guidelines, and ensure profitability through budgeting and expense control.

Job 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 aClinical Study Manageryou 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:

• 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.

Celerion 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.

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