SCRA

A Leading multinational CRO are seeking to appoint a Senior Clinical Research Associate to work on regional studies. The successful SCRA will be responsible for site identification, feasibility, monitoring, site management and close out visits in accordance with GCP Guidelines.

Main Responsibilities (to include but not be limited to):

+ Conduct all levels of Monitoring visits

+ Act as LCRA for Global studies, responsible for the coordination of CRAs

+ To provide training and mentoring for site staff and colleagues where needed

+ Develop monitoring plans, eCRF and protocols as required

+ Actively participate in investigator meetings

Skills/Experience:

+ Educated to degree level in Science/Life Science

+ Previous experience within a CRO

+ Previous SCRA experience/4+ years experience as a CRA

+ In-depth understanding of at least 3 therapeutic areas

+ Thorough understanding of clinical research principals and processes

+ Excellent communication, interpersonal and organisational skills

This is a fantastic opportunity for the successful candidate to secure a permanent position within a reputable organisation.To find out more about Real please visit www.realstaffing.com