Senior Clinical Trial Associate/Site Engagement Manager (m/w/d)

UCB S.A.; Mettmann, Monheim; Vor Ort; EUR 60.000 - 100.000; Vollzeit

Zusammenfassung

Join a forward-thinking biopharmaceutical company as a Senior Clinical Trial Associate/Site Engagement Manager. In this pivotal role, you will engage with high-performing clinical sites, ensuring compliance and quality in clinical trials. Collaborate with diverse teams and stakeholders, leveraging your expertise to drive successful study outcomes. With a strong focus on patient safety and regulatory adherence, this position offers a dynamic environment where your contributions will create real value. If you are ready to make a meaningful impact in the field of neurology and immunology, this opportunity is for you.

Qualifikationen

• 5+ years in Pharmaceutical/Biotech/CRO industry.
• 3+ years of experience in clinical trial monitoring.

Aufgaben

• Manage all site-related activities from feasibility to trial end.
• Develop and execute a Site Engagement Strategy.
• Conduct site visits to ensure patient safety and trial quality.

Kenntnisse

Clinical Trial Monitoring

GCP Knowledge

Communication Skills

Site Engagement

Fluency in English

Fluency in German

Ausbildung

B.S. in Life Sciences

M.S. in Life Sciences

Jobbeschreibung

Make your mark for patients

We are looking for aSenior Clinical Trial Associate/Site Engagement Manager (m/w/d)who is experienced, collaborative, and detail-oriented to join us in our Development Solutions team, based in Germany.

About the role

As aSenior Clinical Trial Associate/Site Engagement Manager (m/w/d), you will engage, develop, and manage a network of high-performing sites to ensure high-quality site performance in clinical trials. You will leverage your clinical operational and therapeutic expertise to support the execution of UCB's clinical studies and ensure compliance with regulatory requirements.

Who you’ll work with

You will work with a diverse and collaborative team, engaging with clinical sites to build and maintain strong relationships with investigators and staff. You will also collaborate with internal and external stakeholders, including third-party vendors, to support Clinical Project Managers in delivering studies within planned timelines and quality standards.

What you’ll do

• Responsible forall monitoring and site-related activitiesfrom feasibility to trial end.
• Develop and execute a Site Engagement Strategy.
• Evaluate and screen high-quality investigational sites.
• Conduct site visits (on-site and remote) to ensure patient safety and trial quality.
• Collaborate with study teams and vendors to support study management tasks.
• Train CRO and site personnel on trial-specific requirements.

Interested? For this role we’re looking for the following education, experience, and skills

• B.S. degree in a life science/biological related field (M.S. preferred).
• Minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry.
• At least 3 years of experience in monitoring trials in clinical development (preferably phase 2-4).
• Strong knowledge of GCP and regulatory requirements.
• Excellent communication skills,fluency in English and German is a must, additional languages are a plus.
• Ability to travel at least 50%of the time, predominantly within the DACH region, including overnight stays and possible global travel.

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

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.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [e-mail]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.