Important pharmaceutical service company


You will monitor the progress of your project(s) and provide regular updates to internal and if applicable external stakeholders, such as the sponsor / client. As a CPM you will be ultimately responsible for ensuring that your project is completed just in time within budget and with the right quality.


• Initiating and managing clinical projects in accordance with all relevant guidelines, legislation and SOPs;

• Monitoring the progress of the clinical trial in relation to the project plan and previously defined performance indicators in terms of quality and budget;

• Identify risks and develop and implement plans to mitigate risks in collaboration with team members and other stakeholders;

• Act as a daily point of contact for the sponsor and all members of the project team;

• Develop research-specific documents;

• Reporting the progress to the internal project team, the internal and if applicable external stakeholders;

• Negotiating contracts with research centers and suppliers;

• Managing project finances in accordance with the (sponsor) contract and budget;

• Provide input for proposals and budgets and play a role in bid defense meetings.


• Bachelor or Master graduate in life science;

• Excellent communication, negotiation and organizational skills;

• Fluent in English

• Experience with managing a budget and a team;

• 5/6 years experience as a CRA or CPM PHASE1 is a plus

• Leadership skills, helicopter view;

• Knowledge of Good Clinical Practice (GCP), Project Management (PMP)

Job Types: Full-time, Permanent



Please send a CV, mentioning the authorization for processing personal data in accordance with law 196/2003 and  the position,

L'offerta di lavoro si intende estesa a entrambi i sessi (L. 903/77). Aut. Min. Lav. prot. nr. 1417 del 22/01/2007.