Cra I

hace 7 días

Madrid, España KCR A tiempo completo

**CRA I / CRA II**

**Location: Spain (home-based)**

**The duties associated with the role include**:

- Performing site visits and monitoring activities in accordance with protocol, GCP/ICH Guidelines and other applicable requirements,
- Ensuring overall integrity of study and adherence to guidelines, protocol and regulations,
- Taking an active role in the project team by providing feedback and suggestions for successful completion of the project,
- Maintaining quality control of assigned parts of Trial Master File (incl. site related documentation),
- Participating in teleconferences and meetings with Sponsor or/and study staff.

**Requirements**:

- University degree in life sciences/pharmacy/biotechnology,
- At least 1 year of independent monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) according to protocol monitoring guidelines, SOPs, GCP/ICH Guidelines,
- Deep understanding of the conduct of the clinical trial processes,
- Oncology study experience is a big asset
- Available to travel
- Ability to complete tasks in an accurate and timely manner,
- Computer competency,
- Fluent in Spanish and English.

At **KCR** we put our mission**:WE SEE HUMAN BEHIND EVERY NUMBER** into our actions, therefore we offer our Employees benefits that comply with national regulations and provide the coverage that best meets employee needs.

To demonstrate how appreciated your talent and your commitment are, KCR is offering you:

- 1 additional day off for your birthday;
- Onboarding process and induction training to develop deep sector knowledge and complex skills;
- Latest technology and the most advanced equipment and working tools;
- An open culture based on slim processes, in an agile structure with a flat hierarchy and direct access to the Management to share ideas and implement change and continuous improvement;
- Mentoring and training programs related to clinical trials, therapeutic areas, hard and soft skills.

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