Sponsor Dedicated Clinical Trial Assistant in Munich area

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

Zusammenfassung

A healthcare company is seeking a Clinical Trial Assistant (CTA) in Germany to manage and coordinate clinical trials, ensuring efficiency and compliance throughout the study lifecycle. This role offers hybrid flexibility in Munich and focuses on supporting clinical studies by liaising with investigators and service providers. Candidates should have a relevant degree or experience in a similar field, a basic understanding of GCP guidelines, and fluency in both German and English. The company promises a supportive work environment and career development opportunities.

Leistungen

Career Growth & Development

Supportive Work Environment

Competitive Benefits Package

Qualifikationen

• Minimum 2 years of experience in a relevant role or field.
• Good understanding of GCP, ICH Guidelines, and drug development processes.
• Ability to manage multiple tasks effectively.

Aufgaben

• Manage administrative and business activities of clinical trials.
• Prepare and maintain essential study documents accurately.
• Support the submission of applications to Ethics Committees.
• Serve as a liaison between investigators and clinical research teams.
• Assist in audit preparations for Health Authority inspections.

Kenntnisse

Project management

Communication

Time management

GCP knowledge

Fluency in German

Fluency in English

Ausbildung

Degree in Life Sciences or related field

High school degree or equivalent

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!

Learn more about our EEO & Accommodations request here.