As a CRA in our Flexible Solutions department, you are of central importance for the successful execution of complex clinical trials (phases I - III) in Germany.

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

If you want to expand your therapeutic expertise and advance your career in a world-class pharmaceutical environment, this is an excellent opportunity. Join us and see for yourself why more than 90% of the world's top 20 pharmaceutical companies have been our clients for many years!

What you can expect from us:

• a meaningful role in a stable, diverse, successful and respected company
• an attractive and competitive salary, including a 13th-month salary and holiday pay
• a true work-life balance
• flexible working hours and company regulations regarding time off in lieu
• Travel time = working time
• a comprehensive onboarding process with support from your personal mentor
• an open-ended home office employment contract
• an attractive, employer-funded pension plan
• Excellent training and development opportunities within Fortreas, as well as support for your personal training plans.
• Continuous support from your line manager, your team, and over 19,000 colleagues worldwide.

Your tasks:

• 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. during co-monitoring visits to the study centers.
• Participation in customer-specific working groups and other internal projects as a Subject Matter Expert

Her background:

• University degree in a relevant field such as biology, biochemistry, chemistry, health management, pharmacology, (veterinary) medicine, etc.
• Alternatively, completed vocational training in the field of health / nursing, or equivalent professional experience in clinical research (e.g. as a study nurse, research nurse, study coordinator...)
• Professional experience in independent monitoring of clinical trials in Germany, gained at a CRO or a pharmaceutical company
• good knowledge of the applicable German and international regulations for clinical trials such as ICH / GCP
• Good organizational skills, empathy, and a meticulous and detail-oriented work ethic.
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As a CRA in our Flexible Solutions department, you are of central importance for the successful execution of complex clinical trials (phases I - III) in Germany.

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

If you want to expand your therapeutic expertise and advance your career in a world-class pharmaceutical environment, this is an excellent opportunity. Join us and see for yourself why more than 90% of the world's top 20 pharmaceutical companies have been our clients for many years!

What you can expect from us:

• a meaningful role in a stable, diverse, successful and respected company
• an attractive and competitive salary, including a 13th-month salary and holiday pay
• a true work-life balance
• flexible working hours and company regulations regarding time off in lieu
• Travel time = working time
• a comprehensive onboarding process with support from your personal mentor
• an open-ended home office employment contract
• an attractive, employer-funded pension plan
• Excellent training and development opportunities within Fortreas, as well as support for your personal training plans.
• Continuous support from your line manager, your team, and over 19,000 colleagues worldwide.

Your tasks:

• 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. during co-monitoring visits to the study centers.
• Participation in customer-specific working groups and other internal projects as a Subject Matter Expert

Her background:

• University degree in a relevant field such as biology, biochemistry, chemistry, health management, pharmacology, (veterinary) medicine, etc.
• Alternatively, completed vocational training in the field of health / nursing, or equivalent professional experience in clinical research (e.g. as a study nurse, research nurse, study coordinator...)
• Professional experience in independent monitoring of clinical trials in Germany, gained at a CRO or a pharmaceutical company
• good knowledge of the applicable German and international regulations for clinical trials such as ICH / GCP
• Good organizational skills, empathy, and a meticulous and detail-oriented work ethic.
•