Senior Study Start Up Associate

đŸ”„ 29 minutes ago

đŸ‡©đŸ‡Ș Germany – Remote

⏰ Full Time

🟠 Senior

✹ Associate

đŸ‘» Ghost score 10%

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

đŸ’Œ Consulting

đŸ„ 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

‱ Lead site start-up and activation tasks requiring technical depth, with a focus on quality and continuous improvement ‱ Conduct feasibility assessments and site identification ‱ Negotiate site contracts and perform other critical study start-up activities ‱ Provide expertise to Study Start Up team leads and project teams ‱ Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies ‱ Contribute to the development, finalization, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms ‱ Support the Study Start Up Team Lead in developing and executing the plan for country and site distribution

🎯 Requirements

‱ A Bachelor's degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline ‱ At least 3 years of experience or understanding of clinical study start-up requirements and activities ‱ Fluency in the local language and English is essential ‱ Willingness to travel as required (approximately 5%) ‱ Legal right to work in Germany

đŸ–ïž 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

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