CRA - CLINICAL RESEARCH ASSOCIATE Ref.: CRA/ST
COMPANY
Important CRO
ROLE
Important CRO is looking for a Clinical Research Associate with a minimum of two years proven experience in clinical studies.
ONLY CV WITH PROVEN EXPERIENCE AS CRA WITH DM 15/11/11 CERTIFICATION WILL BE TAKEN INTO CONSIDERATION.
Role
-
Managing all aspects of the assigned clinical study activities on remote and site monitoring. These will include the conduction of the Initiation visits, routine monitoring, the close-out of clinical sites and maintenance of the Investigators study files;
-
Monitoring of the assigned study sites according to protocol regulations, SOPs, GCP and ICH guidelines;
-
Providing timely and accurate visit reports;
-
Ensuring that all the site staff involved in the study will receive accurate instructions and tools to ensure patients safety and quality data;
REQUIREMENTS
-
Bachelor’s / Master Degree in Health, Science or equivalent
-
A minimum of two years’ monitoring studies experience
-
Certification as per DM 15/11/2011
-
Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements, is a must.
-
English fluent
-
Personal Skills
-
Strong communication and leadership skills: ability to build both internal and external relationships and cooperate with all professional figures involved in the study
-
Ability to work under supervision
-
Good planning, organizational and problem solving skills
-
Ability to meet deadlines
LOCATION
Florence
home/office based (3/2)
Invia il cv con l'autorizzazione del trattamento dei dati personali in base all’art. 13 del D. Lgs. 196/2003 e all’art. 13 GDPR 679/16 ed il riferimento della posizione all'indirizzo email: uff.firenze@standler.it
L'offerta di lavoro si intende estesa a entrambi i sessi (L. 903/77). Aut. Min. Lav. prot. nr. 1417 del 22/01/2007.