Clinical Research Associate, sponsor-dedicated Home Office - Deutschland

Role Summary

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea offers customers in the pharmaceutical, biotechnology and medical device industries a broad range of clinical development, patient access and technology solutions in more than 20 therapeutic areas. With over 19,000 employees in more than 90 countries, Fortrea is transforming drug and medical device development for partners and patients around the world.

This vacancy is intended for upcoming human resources that we expect to need.

As a CRA in our Flexible Solutions department, you are central to the successful implementation of complex clinical studies (Phases I - III) in Germany.

You will contribute to the development of innovative medicines that set a new standard, particularly in the field of oncology, while working exclusively for one of our most important international customers.

If you would like to expand your therapeutic expertise while further advancing your career in a world-class pharmaceutical work environment, this is an excellent opportunity. Come to us and see for yourself why more than 90% of the world's 20 leading pharmaceutical companies have been our customers for many years!

Responsibilities

• all aspects of site management, from the selection of study centers to the close-out
• Support with training, mentoring and further development of new employees, e.g. B. during co-monitoring visits to the study centers
• Participation in customer-specific working groups and other internal projects as a Subject Matter Expert

Requirements

• University degree in a relevant field such as biology, biochemistry, chemistry, health management, pharmacology, (veterinary) medicine, etc.
• Alternatively, completed professional training in the field of health/care, or equivalent professional experience in clinical research (e.g. as a study nurse, research nurse, study coordinator...)
• Professional experience in independent monitoring of clinical studies in Germany, gained at a CRO or a pharmaceutical company
• Good knowledge of the applicable German and international regulations for clinical studies such as ICH / GCP
• good organizational skills, empathy, and a careful and detailed way of working
• Excellent communication skills in business-fluent German as well as good written and spoken English skills are a must

Fortrea is actively seeking motivated, solution-oriented and creative thinkers who share our passion for overcoming clinical trial obstacles. Our goal is to revolutionize the development process and ensure that life-changing ideas and therapies are made available to patients as quickly as possible. Join our exceptional team and benefit from a collaborative work environment where your personal development is encouraged and you can make a significant global impact. For more information about Fortrea, please visit .

Learn more about our EEO & Accommodations request here.

Benefits

What you can expect from us

• a meaningful job in a stable, diverse, successful and respected company
• attractive and competitive remuneration, including 13th salary and holiday pay
• a real work-life balance
• flexible working hours and company regulations for compensatory free time
• Travel time = working time
• Comprehensive onboarding with support from your personal mentor
• a permanent home office employment contract
• an attractive, employer-financed pension plan
• Excellent training and development opportunities within Fortrea as well as support with your personal training plans
• continuous support from your line manager, your team and over 19,000 colleagues worldwide