As a Clinical Research Associate you will have the unique opportunity to have an exciting career in the field of drug and medical device development as part of an expanding team.
Responsibilities:
· Conduct different types of monitoring visits (pre-study visits, site initiation visits, interim monitoring visits & close out visits)
· Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently
· Perform source document verification and prepare monitoring visit reports, including confirmation and follow-up letter
· Manage the study documentation and other essential trial related documents
· Support regulatory submissions to the Competent Authority
· Participate in Investigator selection/feasibility process
Your profile:
· College/University degree in a health or life science related field (preferably medical doctor or pharmacist)
· 1 year experience as a CRA
· Experience both drug and Medical Device studies is a plus
· Excellent verbal and written communication skills in English
· Advanced skills and experience using Microsoft Office (Word, Excel, Power Point, Outlook)
· Valid driving license
· Demonstrated flexibility in schedule and willingness to travel on a regular basis
· Ability to respond quickly to changing demands and opportunities
· Detail-oriented and efficient in time management
Location: Home Office
We are looking forward to receiving your application with your professional CV in English indicating your salary expectation (monthly, net) via email
Job Type: Full-time
Work Location: Remote