Senior Clinical Research Associate
4 settimane fa
Clinical Trials Expert
At Pharmiweb, we are seeking a highly skilled Clinical Trials Expert to join our team. As a Clinical Research Associate, you will be responsible for the successful execution of clinical trials, ensuring compliance with regulatory requirements and company standards.
Key Responsibilities:
- Contribute to the identification of new sites for clinical trials, analyzing capability and supporting CRMA and CSM in making recommendations for trial inclusion.
- Assume an ambassadorial role to facilitate communication between sites and the Client CPO, increasing the value proposition to investigators.
- Facilitate the preparation and collection of site and country-level documents during all phases of the trial, supporting the CSM in the oversight of Country and Site Trial Master Files (TMF).
- Negotiate investigator remuneration, prepare financial contracts between Novartis and investigational sites and investigators, ensuring adherence to payment schedules.
Requirements:
- 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.
Benefits:
At Pharmiweb, we offer a comprehensive and competitive total reward package, comprising an excellent level of base pay, variable pay, and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career.
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