Sponsor Dedicated Clinical Trial Assistant in Munich area

Munich - Germany

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Are you passionate about advancing healthcare through clinical research As a sponsor-dedicated CTA youll 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!

#LI-GQ1#LI-Hybrid

Learn more about our EEO & Accommodations request here.

Required Experience:

Junior IC