Project Coordinator Home Based Milan, Italy

22 set - Milano
Labcorp

**Job Overview**:
Do you dream about working for an employer who wants you to reach your full potential? Are you passionate about making a difference to the lives of others? Is your aspiration to become a Clinical Project Manager working on global clinical studies? Covance by Labcorp has supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. In 2019, we established our first Project Management Academy as our centre of excellence to identify early talent in becoming our future Covance Project Managers, since then we have gone from strength to strength in building our Project Management Academy hubs across the globe. We now have a new opportunity fo you to join our Project Management Academy, home based Italy. You will be working on global clinical studies alongside our Global Clinical Project Managers across a range of therapy areas such as Oncolgy, Cardiovascular, Infectious Diseases and many others. Join Covance by Labcorp and together we really can change the world in advancing healthcare, making a difference to peoples lives everyday.
- Have you completed a life science degree and are taking the first steps on your career path.




- Have you have been working within clinical research and realise that your true passion lies in project management
- Are you a CRA looking to change direction
- Are you already a Project Coordinator but not benefiting from a structured tailor made training programme that allows you to fulfill your potential at the right time and accelerate your Project Management career.
- Can you demonstrate leadership skills, exceptional communication skills and the ability to organise and manage competing priorities. This could be the start of a whole new journey.
**Education/Qualifications**:
University/college degree, or certification in a related allied health profession (i.e. nursing, medical or laboratory technology)
- Knowledge of the clinical trial process preferred
- Computer competency with various programs (e.g., Microsoft Word, Excel, Project, Access and Power Point)
- Ability to develop accurate study related documents with mínimal supervision
- Ability to communicate verbally and in writing
**Experience**: - Some previous relevant industry experience
- Additional experience may be submitted for education requirements

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