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Clinical Trial Manager

Pubblicato il 11-09-2026 - NOUSCOM in Roma

Nouscom is a private clinical stage immuno-oncology company developing next-generation, off-the-shelf and personalized cancer vaccines. Our proprietary viral vector platform has the capacity to encode for large payloads of neoantigens or other immunomodulators and is clinically demonstrated to safely and potently harness the power of the immune system.

We are looking for a Clinical Trial Manger .

The Clinical Trial Manager:
Directs and/or supports the planning and conduct of a clinical trial phase I to III, in-house and outsourced to a Contract Research Organization (CRO) in compliance with company processes, ICH-GCP and regulatory requirements;
Participates/directs CRO management and vendor oversight of outsourced activities;
Coordinates and participates in co-monitoring of clinical trials;
Performs assigned responsibilities to ensure timely achievement of departmental goals and objectives related to clinical trials.

Responsibilities
Participates in the CRO selection process and periodic CRO/vendor performance assessment
Contributes to development of clinical study protocols,



trial budgets and project plans
Contributes to country and site selection for clinical trials
Assists in planning and operational execution of clinical trial supply needs
Takes responsibility in maintenance of clinical trial registries and related databases
Serves as point of contact to CRO and vendors
Maintains a strong knowledge of the protocoland study procedures
Reviews and prepares study plans and manuals (Patient Information Sheet and Informed Consent Form, Project Plan, Monitoring Plan, Communication Plan, Pharmacy Manual, Investigator Site File, etc.)
Approves country/site PIS/ICF prepared by CRO and oversees timely PIS/ICF implementation on site level
Develops and implements Vendor Oversight Management Plan (VOMP)
Leads and/or supports preparation and conduct of bid-defense, kick-off, SMB and investigator meetings
Ensures that essential documents are in place prior to site initiati

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