Clinical Trial Associate (m/f)

REFERENCE NUMBER:

406474/6

MY DUTIES:

-Ensure the training and the information of the participating physicians regarding the study
-Verify the dispensation of the material necessary for the study
-Fill out the CRFs from the source data without interpretation or modification under the supervision of the physician in charge of the center
-Ensure that adverse reaction reports (with the participating physician and project partners) are made to the sponsor to manage requests for clarification
-Verify and stimulate the activity of participating physicians by anticipating problems and taking corrective actions
-Track adverse events under the responsibility of the attending physician
-Classify archive documents and data enter traceability
-Manage and archive the administrative and regulatory documents of the study

MY QUALIFICATIONS:

-Experience in Clinical Trials
-Medical speciality in oncology
-Proper English skills are highly recommended

MY BENEFITS:

-A highly motivated team and an open way of communication

ABOUT HAYS:

With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

MY CONTACT AT HAYS:

My contact person
Anna-Elisa Hochreiter

Reference number
406474/6

Contact
E-Mail: [email protected]