Senior Clinical Project Manager
Key responsibilities
- The Clinical Project Manager is responsible for the feasibility, selection, set up, conduct and closure of a clinical trial interventional and/or NIS/observational within the allocated countries (IT and other EU Countries), in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures.
- The Clinical Project manager is responsible for the operational management of clinical studies, ensuring the compliance with timelines, milestones and budget.
- The Clinical Project Manager will act as the main line of communication to relevant stakeholders and provides input to feasibility, study design, budget development and ensures progress reporting (resources, budget and timelines)
- The Clinical Project Manager leads the monitoring team(s)
in the designated country/countries for his/her trials and ensures the team is trained properly
- Provides input on study related documents (e.g. ICF, CRF, monitor plan, protocol, study Procedure Manual etc.), set-up and maintain study files
Who are you You are a professional with at least 3-5 year of experience in this role, in the context of clinical operations.
Previous experience in CRO is preferred.
Complete your profile
- Able to work in a team;
- High organisational and analytical skills;
- Efficiency oriented;
- Able to work independently;
- Deep knowledge of Regulation
- Good English
- The Clinical Project Manager is responsible for the feasibility, selection, set up, conduct and closure of a clinical trial interventional and/or NIS/observational within the allocated countries (IT and other EU Countries), in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures.
- The Clinical Project manager is responsible for the operational management of clinical studies, ensuring the compliance with timelines, milestones and budget.
- The Clinical Project Manager will act as the main line of communication to relevant stakeholders and provides input to feasibility, study design, budget development and ensures progress reporting (resources, budget and timelines)
- The Clinical Project Manager leads the monitoring team(s)
in the designated country/countries for his/her trials and ensures the team is trained properly
- Provides input on study related documents (e.g. ICF, CRF, monitor plan, protocol, study Procedure Manual etc.), set-up and maintain study files
Who are you You are a professional with at least 3-5 year of experience in this role, in the context of clinical operations.
Previous experience in CRO is preferred.
Complete your profile
- Able to work in a team;
- High organisational and analytical skills;
- Efficiency oriented;
- Able to work independently;
- Deep knowledge of Regulation
- Good English