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Clinical Trials Assistant 1 (m/w/d)
IQVIA
Sponsorship not confirmed
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About the job
At IQVIA, our Clinical Functional Service Partnership (CFSP) model offers the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA. As a Clinical Trials Assistant 1 (m/w/d) within Clinical FSP, office-based in Frankfurt, you'll gain hands-on exposure to real study operations, build foundational expertise alongside experienced CRAs and Project Managers, and develop a clear path toward future clinical research roles, all within a global organization dedicated to transforming healthcare through human science and data science. Key Responsibilities: Maintain and update Trial Master Files (TMF) and study documentation. Support document preparation, filing, tracking, and archiving. Review study files for completeness and compliance. Coordinate clinical trial supplies and tracking records. Assist with CRF tracking, study queries, and data workflows. Act as a key contact for project communications and documentation. Support departmental quality and process improvement initiatives. What You'll Bring: Passion for clinical research and healthcare. Life science university degree preferred. Knowledge of clinical research processes and legal guidelines. Fluent language skills in German on at least C1 level and good command of English. Proficiency in Microsoft Office (Word, Excel, PowerPoint). Strong organisation skills and attention to detail. Ability to manage multiple priorities and meet deadlines. Effective communication skills with the ability to work collaboratively across teams. Willingness to develop into a Junior CRA role (m/w/d) and the flexibility to regular business travel, preferably with a valid driving license class B. Ability to start on 1 January 2027. Benefits: Permanent employment contract. This role might offer career development into a Junior CRA role (m/w/d). Competitive compensation and benefits package. Flexible working schedules and occasional home-office after onboarding. Job Data by YubHub .
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