Clinical Quality Lead

il y a 2 jours

Brainel'Alleud, Belgique UCB S.A. Temps plein

**Make your mark for patients.**

We’re here because we want to build the future and transform patients’ lives for the better.

At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.

An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?

To strengthen our **Research and Clinical development team**, we are looking for a talented individual to fill the position of **Global Clinical Quality Lead** based in Braine l’Alleud, Belgium

**You like to work in an environment where you will**:

- Partner with internal and external business partners in driving quality into the clinical development portfolio across the UCB sites and departments and provide Clinical Development Quality input to cross functional teams dealing with complex and/or important projects and issues
- Develop robust clinical quality risk management programs
- Partner with departments within Development Solutions in driving quality into the clinical activities across the UCB sites
- Provide mentoring and guidance to other members of the Clinical Development Quality team, support the Global Head by deputizing for them at meetings on request, and contribute to planning and resource prioritization decisions for Clinical Development Quality activities
- Organize, manage and empower teams to execute quality strategies to minimize quality risks
- Assure that systematic and planned actions are established to ensure that clinical trials are performed and data generated, documented and reported in compliance with GCP and applicable regulatory requirements and company procedures

**Interested? For this position you’ll need the following education, experience and skills**:

- You have an in-depth knowledge and understanding of ICH-GCP, applicable regulations (domestic and international), quality principles, relevant business processes and techniques.
- You have 10 plus years of background, knowledge and experience of clinical research in Pharma industry or with a CRO, including minimum 2 to 3 years experience in Clinical Quality
- You have experience managing regulatory GCP routine and /or Pre-approval inspections.
- You have effective communication skills by having the ability to articulate oneself and be a good listener
- You are adaptable and flexible to change, strong leadership skills when necessary
- You can influence senior management and external peers on project related issues
- You demonstrated professional maturity in stressful situations or conflicts.
- You are skilled and experienced at operating in a cross-cultural team environment and understand principles of cost-and time efficiency
- English proficiency is required
- French proficiency is desirable

**Why you should apply**

We can offer you an informal and open working environment that does not lock scientists into structure and hierarchy. Freedom to take space to pursue your own ideas and make a difference.

Opportunity to gain internal and external visibility through interactions with other UCB teams and with world-renown academic investigators. Opportunity to grow both as a drug hunter and leader through participation in project teams and our career/personal development programs.

At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees - just as we do for the patients we serve.

RANDATUCB

**About us.**

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.

At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.

UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.

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