Job Title: Clinical Research Associate (CRA) – 0.8 FTE
Location: Austria
Duration: 12-Month Contract
Travel: 60–80%
About the Company
Join a leading global contract research organization (CRO) that partners with pharmaceutical, biotechnology, and medical device companies to advance innovative therapies. The organization is known for its commitment to high-quality clinical research and supports employees in professional growth and development while contributing to meaningful medical advancements worldwide.
Role Overview
We are seeking an experienced Clinical Research Associate (CRA) to manage and coordinate clinical trial site activities in Austria on a 12-Month Contracted basis. In this role, you will ensure compliance with ICH GCP, FDA regulations, local laws, and company SOPs, while maintaining strong relationships with investigational sites and project teams. This is a 0.8 FTE position with significant travel (60–80%).
Key Responsibilities
* Conduct site visits to monitor clinical trial progress, protocol adherence, and regulatory compliance.
* Manage and maintain essential trial documentation to ensure data integrity and audit readiness.
* Represent the organization in the global clinical research community and maintain collaborative relationships with sites and client personnel.
* Assist project or clinical team managers on assigned projects and take a lead role when required.
* Evaluate medical research data and ensure high-quality reporting.
Requirements
* University degree in a science-related field or certified healthcare professional (or equivalent).
* Minimum 5 years of clinical research monitoring experience with demonstrated expertise in all aspects of CRA responsibilities.
* Fluency in English and German.
* Valid driver’s license.
* Expert knowledge of GCP, FDA regulations, and clinical monitoring standards.
* Strong attention to detail, problem‑solving abilities, and flexibility in a dynamic environment.
* Ability to work independently and collaboratively within a team.
* Proficiency in Microsoft Office; ability to learn study-specific software.
* Experience mentoring or training junior CRAs.
* Strong customer focus and ability to build effective site relationships.
Why Join Us
* Contribute to innovative clinical research that impacts patient lives.
* Flexible 0.8 FTE arrangement to support work‑life balance.
* Opportunity for professional development and mentoring.
* Join a collaborative global team in a supportive and dynamic environment.
Note
Full COVID-19 vaccination required; accommodation requests considered.
Apply Now
Apply now to join a highly collaborative team and help drive the success of meaningful clinical trials.
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