Our leading niche CRO client is currently looking to hire a permanent CRA to work on rare disease projects.
As a CRA you will be responsible for the successful conduct of clinical trials and serve as main contact for the investigative site by representing our client in a professional manner.
What You'll Do
*Conduct evaluation, initiation, monitoring and close out visits
*Assist with regulatory and study start-up activities including contract and budget negotiations
*Ensure clinical data integrity and meet study timelines
*Provide ongoing updates and support to project management
*Attend global project meetings including investigator meetings and global team teleconferences
*Complete assigned training programs in drug development processes, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements.
What You Bring
*2-3 years clinical research experience as a CRA or related profession
*Life science background
*Excellent knowledge in ICH-GCP and regulatory requirement
*Fluent in Italian and English Language
Key People is a specialist international recruitment consultancy with over 25 years' experience of working within the life sciences, biotech, healthcare and CRO industries. Our experienced and dedicated clinical research related consultants have a long history of success, excellent technical knowledge and a flexible, consultative focussed approach to recruitment.
Please contact Mark Cussens, Clinical Research Recruiter on
Tel: +44 1727 817623 or email: firstname.lastname@example.org
Tel: +41 4350 86620 or email: email@example.com
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