Clinical Trial Manager | Referent Klinische Studien | Disclosure Specialist (m|w|d)

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Do you maintain an overview even with complex regulatory requirements and feel at home in the environment of clinical trials and their transparency? Do you work in a structured, detail-oriented manner and convince with sound knowledge in the field of Clinical Trial Disclosure and regulatory requirements? Then we look forward to getting to know you!

For our client, we are looking for you as a Clinical Trial Manager | Referent Klinische Studien | Disclosure Specialist (m|w|d) in permanent employment at the earliest possible date - remote or at the location in Monheim.

Our client offers you:

• MONETARY BENEFITS: An attractive remuneration including vacation and Christmas bonuses
• WORK-LIFE-BALANCE: A 37.5-hour week, 30 days of vacation and flexible working hours as well as the possibility to work from home
• CORPORATE BENEFITS: Attractive discounts at many well-known companies
• FURTHER TRAINING: Professional onboarding as well as regular employee development discussions
• APPRECIATION & COMMITMENT: Competent support at all times with an excellent top employer (Kununu Score: 4.8)

Your tasks:

• You develop and manage disclosure strategies for clinical trials, taking regulatory requirements into account, and work closely with internal and external stakeholders
• You create, review, and maintain registration documents throughout the entire study lifecycle and ensure data consistency across different platforms
• You coordinate the timely publication of study results, including quality control and coordination with relevant interfaces
• You ensure compliance with quality standards, SOPs, and regulatory requirements and support audits as well as inspections
• You work with relevant systems and tools, monitor data quality, and coordinate external service providers if necessary

Your profile:

• You have a completed degree, e.g., in Chemie or Biologie (at least Bachelor), as well as relevant experience in clinical research, e.g., in study management, data management, or Regulatory Affairs
• You have experience with clinical trials
• You possess sound knowledge of regulatory requirements as well as experience with registration platforms
• You work data-driven, detail-oriented, and are confident in handling complex processes and guidelines
• You have strong organizational, communication, and project management skills and enjoy working in international teams
• You speak and write English fluently

Tired of long and tedious processes?

Send us your CV today and we guarantee you the fastest and most uncomplicated processing.

Please refer to the reference number in your application: 8672-C

If you are not sure whether you meet all the criteria, please feel free to apply anyway. We look forward to your application and also offer you other exciting commercial vacancies.

Advantages of placement through TRICONNECT:

• Free & transparent advice or placement with your desired employer
• Management and advice during salary & contract negotiations
• Coordination & appointment management of all interviews with our client
• Tips and tricks for the perfect interview
• On request, accompaniment to the job interview