Freelancer CRAs CONTRACTS Italy

2.JOB FUNCTIONS/RESPONSIBILITIES:
*Knowledgeable of Clinical Research's SOPs regulations, Systems and principles of investigator recruitment.
*Recruitment of investigators.
*Independent and proactive co-ordination of all the necessary activities required to set up and monitor a study, including the following:
-Identify investigators.
-Help, when requested, in preparation of Regulatory submissions.
-Design patient information sheets and consent forms.
-Co-ordinate documents translation, verification and back translations where required.
-Ensure timely submission of protocol/consent documents/safety reports for ethics/IRB approval according to local requirements.
-Placement and initiation visits.
-Conduct regular monitoring visits
3.QUALIFICATIONS/EXPERIENCE REQUIRED:
*Medical/science background and relevant experience.
*Ability and willingness to travel at least 50% of the time (international and domestic: fly and drive)
*Ability to review and evaluate clinical data arising from aptitude and have the required level of experience in Clinical Research.
*Computer literacy required.
*Foreign language skills desirable.
*Current full driving licence essential.
*Good oral and written communication skills.
If you would like to discuss this role in greater details or your application/suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.

We also have a broad variety of other Clinical Research vacancies available in Italy and throughout
For a confidential consultation call Iolanda Oddo on 0044 (0) 207 255 6665 or email your CV to [Email hidden]