Senior Clinical Research Associate

vor 2 Wochen

Wien, Österreich Icon plc Vollzeit

Overview

As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

**Responsibilities**:
The Clinical Research Associate is ultimately responsible for the successful management of investigator sites and monitoring activities for assigned clinical studies throughout the trial lifecycle. Key responsibilities include:

- Full ownership of investigator sites for assigned studies, with responsibility for the successful management of the site right through to close-out, in accordance with the clinical monitoring plan.
- Developing effective relationships with investigator site staff (at sites in Southern Germany and Switzerland) to ensure that key clinical metrics are met.
- Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

**Qualifications**:
To enable success in this position you will have:

- At least 1.5 years as an independent CRA, including conducting monitoring visits for clinical trials, from either a pharmaceutical company or a CRO environment.
- A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
- You will be educated to degree level in a life science discipline or be a licensed healthcare professional.
- Fluency in German and English is essential
- Scientific degree (BSc, MSc or PhD), have equivalent experience or be a licensed healthcare professional.

**Salary**: From 0.01€ per year

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