We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job DescriptionJoin our international team as a key support for clinical research projects. In this role, you will streamline communication, maintain systems, and manage documents & information to support the success of our clinical research projects.
This position is reserved for candidates belonging to protected categories under Italian Law 68/99.
Your responsibilities will include:
- Maintenance of databases, tracking systems, and management of large volumes of documents
- Acting as the primary communication point for investigative sites and internal departments
- Coordination of site-specific query resolution, project training, and system access for site teams
- Assistance with meeting arrangements, including preparation of draft agendas and minutes
- Handling of incoming correspondence and calls efficiently
- College/University Degree in Life Sciences
- Prior administrative experience in Clinical Research / CRO environment is preferred
- Full working proficiency in Italian and English
- Proficiency in standard MS Office applications
- Excellent organisational, planning, and problem-solving skills
- Ability to multi-task and work effectively in a fast-paced, team-oriented environment
Base salary range: €28,000 – €41,000 gross annual salary.
Actual compensation: The salary offered within the stated range will depend on objective, job-related criteria, including demonstrated competencies, qualifications, and skills relevant to the position.
Additional compensation: bonus, incentive plans, and other benefits may apply.
Skills Required
- College/University Degree in Life Sciences
- Full working proficiency in Italian and English
- Proficiency in standard MS Office applications (Excel, Word, Outlook)
- Excellent organisational, planning, and problem-solving skills
- Ability to multi-task and work effectively in a fast-paced, team-oriented environment
- Prior administrative experience in Clinical Research / CRO environment
What We Do
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
