drjobs Senior Clinical Research Associate/Site Engagement Manager (m/f/d)

Senior Clinical Research Associate/Site Engagement Manager (m/f/d)

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1 Vacancy
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Job Location drjobs

Mettmann - Germany

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Make your mark for patients

We are looking for aSenior Clinical Research 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 UCBs clinical studies and ensure compliance with regulatory requirements.

Who youll 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 youll 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 were 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 skillsfluency 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 8500 people in all four corners of the globe inspired by patients and driven by science.

Why work with us
At UCB we dont just complete tasks we create value. We arent 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 thats 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 . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.


Required Experience:

Manager

Employment Type

Full Time

Company Industry

About Company

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