Clinical Research Associate II (all genders) (full-time, fixed-term for 24 months)

Role Summary

The chance to get things moving with your own strengths? We offer!

A career with growth potential? We offer!

A promising forecast for your future? We offer!

Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will be close to tackling the health challenges of tomorrow with us. Are you passionate about advancing healthcare worldwide and using your know-how to improve the quality of life of patients? And in a challenging working environment that allows you to further develop your own skills? Then you've come to the right place!

As a team member in our diverse Research and Development department, you will make a significant contribution to advancing medical developments with your skills and passion.

Demonstrate your know-how and become part of our own clinical research team in als

Clinical Research Associate II (all genders) (full-time, fixed-term for 24 months)

As a Clinical Research Associate II, you play a key role in the clinical testing of our medicines: You are responsible for the implementation of global studies in Germany. In addition to your monitoring skills, your experience in study management and your process know-how are in demand: within the growing “Clinical Site Management” department, you have a wide range of design options.

Are you looking forward to, among other things

• The opportunity to help shape modern clinical research in a responsible position
• An agile and helpful team that will support you on your way into the world of AbbVie
• An employer that has already been recognized as a “Top Employer” and with the “Corporate Health Award” (more at: )

The position is initially limited to two years - with the aim of long-term collaboration with good performance and successful integration into the team.

• At AbbVie, your individual contributions count — help us build mountains together
• move. Be part of our success, grow with us and achieve more than you want
• can imagine. Sounds like the perfect career opportunity? We look forward to yours
• Application! All we need is a complete resume — everything else

We would be happy to discuss this with you personally.

And if you have any questions? Write us an email – we look forward to hearing from you!

AbbVie is an equal opportunity employer and committed to operating with integrity, driving innovation, changing lives and serving our community. Equal Opportunity Employer/Veteran/Disabled.

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Responsibilities

Specifically, this means

• Study management: You are responsible for a selection of studies - from the selection of centers to implementation and completion.
• Coordination: You work closely with your local CRA colleagues in various study teams and contribute to the on-time project process through forward-looking planning.
• Monitoring: You manage a selection of test centers and monitor the collaboration with partners and authorities as well as the entire site management with your local CRA colleagues.
• Compliance: You ensure that all internal and external specifications are adhered to in your projects and that the test centers are ready for inspection at any time.

Requirements

This is how you make the difference

• Bachelor's degree or equivalent, ideally in a health-related field of study (e.g. medicine, natural sciences, pharmacy)
• At least 2 years of on-site and remote monitoring experience in phase 1-4 clinical trials as well as in-depth knowledge of relevant regulations and standards
• Planning skills, excellent organizational skills and analytical thinking skills, independent and structured way of working
• Excellent social skills, enthusiasm, ability to reflect, flexibility and persuasiveness
• Fluent German and English skills

About the Company

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

R&D Process Engineering Organization, a part of AbbVie’s Development Sciences organization, is responsible for designing and developing scalable processes to make drug substances and drug products, including synthetics molecules, antibody drug conjugates (ADCs) and genetic medicines, throughout pre-clinical and clinical development stages. Process Engineering also partners with Biologics CMC (Chemistry, Manufacturing, and Controls) Development and Aesthetics R&D functions to provide active engineering support to enable robust process scale-up and manufacturing of biologics drug substances and drug products including toxins and cosmetic active ingredients (CAIs). It drives the development of innovative engineering technologies and creates valuable intellectual property through the composition of matter and chemical/bio-chemical processes resulting in cost-effective commercial manufacturing processes for quality products.