Legal/R&D Supporter (m/f)

REFERENZNUMMER:

264709/11

IHRE AUFGABEN:

-Draft and negotiate the international agreements focused on the R&D field, as well as confidentiality agreements, preliminary agreements (letters of engagement, letters of intent, etc.), collaboration agreements and co-development agreements with counterparts operating in the R&D field
-Draft and negotiate agreements with CROs (mainly international)
-Review of clinical trial agreement templates to be executed at selected sites for multi-centric clinical trials in the designated countries
-Review of changes proposed by sites to draft clinical trial agreements (between CRO and Site) for the multi-centric clinical trial performance
-Review of regulatory documents necessary to submit and obtain approval for the performance of clinical trials in the designated countries
-Draft and negotiate consultancy agreements and services agreements for R&D
-Draft and negotiate research agreements with universities and other research institutions

IHRE QUALIFIKATIONEN:

-Graduated in law, ideally with a pharmaceutical background
-Profound experience in companies operating in the pharmaceutical field, or in law firms with expertise in the pharmaceutical field or CROs managing clinical trials at an international level
-Experience in managing business and legal professional tasks at an international level
-Excellent command of the English language, both written and verbal as well as a good listening comprehension skills in Italian
-Proficiency in common software applications (Word, Excel etc.)
-Autonomous working style is essential
-Reliability, precision, problem solving skills, confidentiality, flexibility, teamwork orientation, strong spirit of collaboration, stress resistance

WEITERE QUALIFIKATIONEN:

R&D scientist