Clinical Trial Coordinator, Experienced

🕒 June 13

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 $1G Post-IPO Debt on 2023-05

Healthcare Insurance • Biotechnology • Artificial Intelligence

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 (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. • Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. • Assist with periodic review of study files and completeness. • Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. • Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. • Act as a mentor for less experienced Clinical Trial Coordinators and assist with training and onboarding of new colleagues. • May serve as subject matter expert for business processes or lead Clinical Trial Coordinators study teams. • May participate in departmental quality or process improvement initiatives.

🎯 Requirements

• Bachelor’s or higher-level University Degree preferably in life science, or High School Diploma and apprenticeship within the life science, medical or pharmaceutical field or within office management. • At least 2-4 years’ experience as Clinical Trial Coordinator or within another administrative role in clinical research, e.g. as Clinical Trials Assistant, Study Start-Up Assistant. • Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Fluent languages skills in German on at least C1 level and good command of English. • Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint. • Effective communication, organizational and planning skills. • Ability to work independently and to effectively prioritize tasks while working on multiple projects. • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

🏖️ Benefits

• Permanent employment contract. • In-depth training and mentoring. • Home-Office. • Competitive salary and benefits package.