Job Details

Clinical Research Associate I (All Genders) (Full Time, 18 Months Fixed Term)

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.

Willkommen bei AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you are involved in addressing the health challenges of tomorrow. Do you have a passion for advancing global healthcare and improving the quality of life for patients with your expertise? And that in a challenging work environment that allows you to further develop your own skills? Then you are in the right place with us!

As a team member in our diverse research and development department, you contribute significantly to advancing medical developments with your skills and passion.

Showcase your expertise and become part of our own clinical research team in Wiesbaden as:

Clinical Research Associate I (All Genders) (Full Time, 18 Months Fixed Term)

As a Clinical Research Associate I, 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 department "Clinical Site Management", you will have many opportunities for development.

Specifically, this means:

• Study Management: You are responsible for a selection of studies – from the selection of centers to the implementation and completion.
• Coordination: You work closely with your local CRA colleagues in various study teams and contribute through forward-looking planning to the timely project schedule.
• Monitoring: You support a selection of investigational sites and oversee the cooperation with partners and authorities as well as the entire site management with your local CRA colleagues.
• Compliance: You ensure that all internal and external requirements are met in your projects and that the investigational sites are always inspection-ready.

Qualifications

So you make a difference:

• Bachelor's degree or equivalent, ideally in a health-related field (e.g., medicine, natural sciences, pharmacy)
• At least one year of clinically relevant work experience in a medical environment, in the pharmaceutical industry or in a diagnostic company is desirable
• Knowledge of ICH/GCP guidelines as well as the applicable local regulations is desirable
• Planning skills, excellent organizational talent and analytical thinking, independent and structured working method
• Excellent social skills, ability to inspire, ability to reflect, flexibility and persuasiveness
• Fluent German and English language skills
• You will also look forward to:
• The opportunity to shape modern clinical research in a responsible position
• An agile and supportive team that supports you on your way into the world of AbbVie

The position is initially limited to 18 months – with the aim of long-term cooperation in case of good performance and successful integration into the team.

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

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