Sponsor Dedicated Clinical Trial Assistant in Munich area

Fortrea; Deutschland; Hybrid; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

A clinical research organization is seeking a Clinical Trial Administrator to manage and coordinate clinical studies in Munich. This role, offering a hybrid working model, requires a degree in Life Sciences or related fields, along with fluency in German and English. Responsibilities include managing trial documentation, supporting regulatory submissions, and liaising between investigators and service providers. The organization provides career growth opportunities and a supportive work environment, along with a competitive benefits package.

Leistungen

Career Growth & Development

Supportive Work Environment

Competitive Benefits Package

Qualifikationen

• Minimum 2 years of experience in relevant fields alongside a high school degree.
• Understanding of GCP and ICH guidelines, along with the drug development process.
• Ability to function independently.

Aufgaben

• Manage administrative and business activities related to clinical trials.
• Prepare and maintain essential study documents for accuracy and compliance.
• Serve as a central liaison between investigators and service providers.

Kenntnisse

Fluency in German

Fluency in English

Ability to manage multiple tasks

Good computer aptitude

Ausbildung

Degree within Life Sciences, Administrative, Financial or Accounting

Tools

Complex software applications related to clinical trial research

Jobbeschreibung

Are you passionate about advancing healthcare through clinical research? As a sponsor-dedicated CTA, you'll play a pivotal role in managing and coordinating clinical studies, contributing to groundbreaking medical discoveries.

This role is for upcoming future opportunities that may arise at Fortrea

It offers hybrid model possibility in Munich (client-office based).

Key Responsibilities

• Manage the administrative and business activities related to the conduct of clinical trials with investigative sites from study start-up to study closure
• Prepare, review and maintain essential study documents, ensuring accuracy and compliance throughout the trial lifecycle.
• Support the submission of applications to Ethics Committees and Regulatory Authorities, ensuring timely approvals and adherence to local and international guidelines.
• Serve as central liaison between investigators, external service providers and clinical Research associates
• May support Health Authority inspection, pre-inspection activities and/or audit preparation.

Required Qualifications

• Degree within Life Sciences area, Administrative, Financial or Accounting related field preferred, or minimum 2 years working experience in any of these areas in addition to high school degree or local equivalent.
• Basic understanding of GCP, ICH Guidelines, local regulations and of the drug development process
• Experience in managing multiple tasks and to prioritize, setting milestone to meet deadlines.
• Demonstrates ability to function independently
• Good computer aptitude and willingness to learn new systems and applications.
• A plus would be a good knowledge of complex software application related to clinical trial research.
• Fluency in German and in English

What we Offer

• Career Growth & Development: Gain hands-on experience in clinical research with opportunities for professional training and career advancement.
• Supportive Work Environment: Be part of a collaborative and dynamic team, working alongside experienced professionals in a sponsor-dedicated role.
• Competitive Benefits Package that also involve flexible working arrangements, access to wellness programs and feel included by joining Employees Resource Groups to build relationships and expand your network.

Join us in shaping the future of clinical research while building a fulfilling career!

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