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Clinical Project Manager
CelerionRemote - US, United StatesRemotefull_timeVerifiedPosted 16 Jul 2025
About the role
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.
Position Summary:Celerion is looking for a Clinical Project Manager who will be responsible for the independent management of multi-center site activities ensuring compliance to protocol, ICH Good Clinical Practices, Standard Operating Procedures and regulatory and local requirements.
This role will be home based anywhere in the United States. Due to our international footprint, schedule flexibility is important. This position will travel roughly 30% primarily in the US, but could include Europe on an as needed basis.
Essential Responsibilities:Lead the initiation, maintenance and close out activities of multi-center studies in accordance with the protocol, relevant SOPs, Good Clinical Practice, international standards, and regulatory requirementsPlan and procure team resources as needed to complete study activities according to scope, budget, and timelineDevelop and/or oversee development of study plans such as project management (including communication), monitoring, risk management, data management and safety plansCoordinate activities with central laboratories and other external service providers/vendorsReview and negotiate site budgets and contractsInitiate and participate in the development of change orders to sponsor and/or site contracts and budgetsMaintain appropriate and effective communication with sponsor, external service providers, and other internal departments to ensure successful project completion
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.
Position Summary:Celerion is looking for a Clinical Project Manager who will be responsible for the independent management of multi-center site activities ensuring compliance to protocol, ICH Good Clinical Practices, Standard Operating Procedures and regulatory and local requirements.
This role will be home based anywhere in the United States. Due to our international footprint, schedule flexibility is important. This position will travel roughly 30% primarily in the US, but could include Europe on an as needed basis.
Essential Responsibilities:Lead the initiation, maintenance and close out activities of multi-center studies in accordance with the protocol, relevant SOPs, Good Clinical Practice, international standards, and regulatory requirementsPlan and procure team resources as needed to complete study activities according to scope, budget, and timelineDevelop and/or oversee development of study plans such as project management (including communication), monitoring, risk management, data management and safety plansCoordinate activities with central laboratories and other external service providers/vendorsReview and negotiate site budgets and contractsInitiate and participate in the development of change orders to sponsor and/or site contracts and budgetsMaintain appropriate and effective communication with sponsor, external service providers, and other internal departments to ensure successful project completion
Requirements:
- Bachelor's degree required, preferably in science, nursing, other biomedical discipline, or equivalent
- Clinical research experience as a CRA or Research Coordinator is preferred
- Experience in support of business development processes; including budgets, proposals and bid defense planning and execution
- Ability to work across multiple projects
- Experience with renal and hepatic impairment, infectious disease and tobacco studies is an asset
- Flexible and willing to travel up to 30% (regional)
- Excellent problem-solving and decision making skills
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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