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| Job Location | Cambridge |
| Education | Not Mentioned |
| Salary | Salary negotiable |
| Industry | Not Mentioned |
| Functional Area | Not Mentioned |
| Job Type | Permanent, full-time |
Associate Clinical Project ManagerRemote BasedPermanentCompetitive salary + benefits packageClinical Professionals have teamed up with a leader in antibiotic innovation who design new mechanism antibiotics to be specific for the pathogen or infection. They are looking to grow their Clinical Operations team across Europe and so are looking to bring on board an Associate Clinical Project Manager to drive their studies forward.Responsibilities: - CRO oversight activities- Conducts co-monitoring within region- Reviews monitoring reports- Oversees investigator performance- Review of clinical trial documents such as consent documents, study related plans and investigator agreements- Responsible for oversight of Ethics and Regulatory submissions- Reviews and approves essential document packages to enable timely site activation- Responsible for oversight and maintenance of the TMF and completeness at the end of the study- Ensures study inspection readinessRequirements:- BSc or BA in a relevant scientific discipline or RN qualification- Vendor (CRO) oversight experience- CRA experience- Infectious Disease experience would an advantage- A good understanding of the drug development processIf this role is of interest, please send your CV to or call Nadine on to discuss in further detail.