Clinical Research Associate Specialist
15 ore fa
At Engineeringuk, we are seeking a skilled Clinical Research Associate to join our team. As a Senior Clinical Research Associate, you will play a crucial role in identifying new sites for clinical trials and analysing their capabilities.
Responsibilities- Contribute to the identification of new sites for clinical trials;
- Analyse capability and support CRMA and CSM in making recommendations for trial inclusion;
- Assume an ambassadorial role to facilitate communication between sites and the Client CPO to increase value proposition to investigators;
- Facilitate the preparation and collection of site and country-level documents during all phases of the trial;
- Support the CSM in the oversight of Country and Site Trial Master Files (TMF);
- Negotiate investigator remuneration and prepare financial contracts between Novartis and investigational sites and investigators;
- Degree (BA/BS/BSc) in life sciences or qualified nurse preferable;
- Minimum 2 years of independent CRA monitoring experience is mandatory;
- Experience of clinical trial set-up and contract negotiation preferred but not essential;
- EDC working experience;
- Full-time availability;
- The Italian Certification as per DM 15/2011 is required.
We offer a comprehensive total reward package that comprises an excellent level of base pay, variable pay and recognition programs. Our employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career.
Why Choose Us?We are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is on providing a workplace free of discrimination and harassment.
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