Clinical Research Manager

2 weeks ago


Dayton, United States Medix Full time

We are hiring a Clinical Operations Manager at a clinical research site in Dayton, OH The Clinical Operations Manager (COM) is responsible for the oversight of all aspects of Clinical Trial Team activities at a clinical trial site. The COM, in concert with the Site Director and Principal Investigator, is accountable for achieving successful delivery at the project level by meeting Sponsor contractual agreements, regulatory requirements, SOPs and Work Instructions, and quality standards on time and in alignment with enrollment performance expectations.#MedixLS


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    Dayton, United States EVOLUTION RESEARCH GROUP Full time

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  • Dayton, United States EVOLUTION RESEARCH GROUP Full time

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  • Dayton, United States Medix Full time

    We are hiring a Clinical Operations Manager at a clinical research site in Dayton, OH! The Clinical Operations Manager (COM) is responsible for the oversight of all aspects of Clinical Trial Team activities at a clinical trial site. The COM, in concert with the Site Director and Principal Investigator, is accountable for achieving successful delivery at the...


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  • Dayton, United States Applied Research Solutions Full time

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    Dayton, United States EVOLUTION RESEARCH GROUP Full time

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    Dayton, United States Evolution Research Group Full time

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  • Dayton, Ohio, United States Kettering Health Full time

    Overview: Kettering Health is a not-for-profit system of 13 medical centers and more than 120 outpatient facilities serving southwest Ohio. We are committed to transforming the health care experience with high-quality care for every stage of life. Our service-oriented mission is in action every day, whether it’s by providing care in our facilities,...


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  • Dayton, United States EVOLUTION RESEARCH GROUP Full time

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    We are seeking Board Certified Physician to join this team as a Principal Investigator. As a key member of a clinical research company, you will play a crucial role in overseeing and conducting clinical trials. In this role, you will ensure protocols adhere to regulatory requirements and ethical standards, supervise data collection, collaborate with...

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