Medical Research Professional

22 ore fa


Italia Novartis A tempo pieno

**Job Overview**

A Medical Research Professional plays a crucial role in ensuring the success of clinical trials. This position involves monitoring patient data and study information at clinical trial sites, as well as ensuring researchers adhere to research protocols, regulatory requirements, and best clinical practices.

Main Responsibilities:

  • Conduct site initiation visits, ensure site personnel are trained on trial-related aspects, and perform continuous training for amendments and new personnel.
  • Manage assigned study sites, conducting phase I-IV protocols according to the Monitoring Plan and Novartis procedures.
  • Perform continuous site monitoring activities (onsite and remote) and implement site management activities to ensure compliance with protocol, ICH/GCP, global and local regulation.
  • Document site processes and identify deficiencies, working closely with site personnel to mitigate risks and improve processes.
  • Promote a culture of compliance and advocate adherence to highest standards and ethical integrity.

About the Role

The ideal candidate will have a degree in a scientific discipline and at least 1-year experience as a CRA in a pharmaceutical company or CRO. Fluency in Italian and good knowledge of English (B2 level) are also required. Willingness to travel across Italy is necessary.

Benefits

Novartis offers a competitive salary, which includes an estimated **€55,000 - €65,000** per year, depending on experience. You will also receive benefits and rewards as outlined in the Novartis Life Handbook.

Additional Information

This role is part of the Development division within Innovative Medicines at Novartis Farma S.p.A. The successful candidate will be employed full-time as a regular employee with no shift work required.



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