Clinical Trials Associate

🔥 12 hours ago

🇩🇪 Germany – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 Ghost score 10%

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. • Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions. • Support the preparation of study-related materials, such as informed consent forms and case report forms. • Work with cross-functional teams to facilitate communication and ensure smooth trial execution. • Contribute to the tracking and reporting of clinical trial metrics and milestones. • Assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

🎯 Requirements

• Bachelor's degree in a scientific or healthcare-related field. • Prior experience or strong interest in clinical research. • Knowledge of clinical trial processes, regulations, and guidelines. • Excellent organizational and communication skills. • Ability to work collaboratively in a fast-paced environment with attention to detail. • Willingness to travel as required (approximately 10%) • Fluency in German and English language • Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways