Study Coordinator Data Entry Freelance in France
The main task will be to ensure that the data collected by the research team is recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and relevant regulatory requirements as external member of the research team of the site.
Also, assist and advise the research team during the progress of a clinical trial and participate in investigator Meetings.
A Bachelor's or higher graduate degree within a science related field or alternatively licensed healthcare training or equivalent experience is also necessary (nursing equivalent qualification is acceptable) and has excellent English language skills.
You can apply for this role by e-mailing your CV to email@example.com or telephoning +44 (0) 207 255 6600.
Tél. : 44-0 207 255 6600