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.