Erfahrener Clinical Trial Coordinator – Home Office

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Assist Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems, including the Trial Master File • Prepare, handle, distribute, file, and archive clinical documentation and reports according to the scope of work and standard operating procedures • Conduct periodic reviews of study files and completeness • Support preparation, handling, distribution, and tracking of Clinical Trial Supplies • Coordinate tracking and management of Case Report Forms, queries, and clinical data flow • Serve as a central contact for designated project communications, correspondence, and associated documentation • Mentor less experienced Clinical Trial Coordinators and support training and onboarding of new colleagues • Serve as a subject matter expert or lead Clinical Trial Coordinators study teams when required • Participate in departmental quality or process improvement initiatives

🎯 Requirements

• Bachelor’s or higher-level University Degree, preferably in life science • Alternatively, High School Diploma and apprenticeship within the life science, medical, pharmaceutical, or office management field • At least 2–4 years’ experience as a Clinical Trial Coordinator or in another administrative clinical research role • Knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice and International Conference on Harmonization guidelines • Fluent German language skills at least at C1 level • Good command of English • Working knowledge of Microsoft Word, Excel, and PowerPoint • Effective communication, organizational, and planning skills • Ability to work independently and prioritize tasks across multiple projects • Ability to establish and maintain effective working relationships with coworkers, managers, and clients • Ability to work from a home office anywhere in Germany • English CV and motivation letter required for application

🏖️ Benefits

• Permanent employment contract • In-depth training and mentoring • Home-office work anywhere in Germany • Competitive salary and benefits package