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Clinical Research Associate (CRA) f/m/d

Germany
Full-time
Hybrid
Competitive Salary
Open: 22.08.25
Close: 30.09.25

Job Description

We are looking for an experienced CRA (Clinical Research Associate) to join our Project Delivery team in Germany.  

The CRA plays a crucial role in ensuring the successful planning, conduct and monitoring of clinical trials, from the initiation of the trial sites to completion. They ensure that clinical trials are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines and study protocols, with a focus on patient safety, data integrity and adherence to timelines. They serve as an important link between the project manager, clinical trial sites and the sponsor to ensure ethical, efficient and effective trial conduct. 

 

Responsibilities

In this role, you will serve as an integral member of the study team. Your responsibilities will include preparing monitoring visit reports, participating in both study team and investigator meetings, and supporting site selection as well as recruitment potential assessments. Additionally, you will oversee staff training related to study content, logistics, documentation, and data collection, while actively working to motivate site personnel. Responsibilities include 

  • Plan, conduct, and follow up on monitoring visits for phase I-IV clinical trials. 
  • Recruit investigators. 
  • Ensure accurate and prompt delivery of study data and documents. 
  • Provide support to trial sites when issues occur. 
  • Manage trial sites independently. 
    • Assist the project manager with coordination and organisation. 

Requirements

  • A degree in natural sciences or significant clinical research experience is required; alternatively, extensive relevant work within clinical research may substitute for formal qualifications. 
  • Minimum of 2 years’ experience or completion of at least 100 independently managed centre visits. 
  • Thorough understanding of ICH-GCP standards. 
  • Demonstrates absolute reliability and precision. 
  • High level of independence with proven ability to work autonomously. 
  • Structured, self-directed approach complemented by strong organisational and communication abilities. 
  • Excellent interpersonal skills and substantial experience collaborating with investigators. 
  • Great communication skills to support effective interaction with sites. 
  • Advanced IT proficiency, including mastery of MS Office, spreadsheets, and database management. 
  • Willingness to travel extensively, comprising approximately 50% – 70% of working hours. 
  • Proficiency in both oral and written English and German. 

What Astrum Offers

  • Flexible working hours through flexitime. 
  • Competitive salary. 
  • Employer contribution to company pension scheme. 
  • Join our dynamic company for diverse development opportunities within a supportive team and streamlined structure. 
  • Enjoy an attractive work environment, flexible hours, and options to work from home or connect with colleagues in person. 
  • Benefit from training tailored to your experience, a dedicated contact person, and regular opportunities for advancement. 
  • Monitor visits are planned as needed, prioritizing quality and efficiency. 
  • Your ideas for process improvement are encouraged and valued. 

About Astrum

Astrum is a pan-European Contract Research Organisation (CRO) formed from leading clinical research companies across Spain, Portugal, Germany and France. We deliver end‑to‑end clinical development services, from early Phase I studies to late‑phase trials, supported by specialist expertise across an array of clinical services.

With over 25 years of combined experience and more than 300 clinical professionals across Europe, we are committed to scientific excellence, flexibility and transparency—helping our partners bring new treatments to patients faster, safer, and always with confidence.

Interested in the role?

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