Clinical Trial Designer

Job not on LinkedIn

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✍️ Designer

👻 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

• Create high-quality data collection tools for new clinical trials • Facilitate design, development, documentation, testing, and implementation of clinical eCRF databases • Design eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio • Interpret detailed data collection requirements from protocols and study team input • Work with libraries and create new forms when suitable forms do not exist • Produce annotated study books • Design workflows, dynamic forms, and events • Validate study forms and schedule designs • Develop test steps and perform quality control of forms • Support data integrations, local lab management, and coding functionality • Contribute to post-production form changes in live trials • Apply lessons learned between study builds • Conduct study team meetings to communicate scope, timelines, and project requirements • Maintain knowledge of regulatory requirements, industry trends, benchmarks, and data management best practices

🎯 Requirements

• BA/BS degree; commensurate experience will be considered • Minimum of 2 years of Clinical Data Management experience using electronic data capture systems • Effective oral and written presentation and communication skills • Strong attention to detail and commitment to high quality work, customer service, and minimal errors • Ability to manage multiple project tasks and deliverables in a fast-paced, constantly changing environment • Experience in planning and management of clinical trials in the biopharmaceutical industry or related field preferred • Familiarity with clinical research processes and CDISC/CDASH/SDTM standards preferred • Design experience using Oracle InForm/Central Designer or Veeva CDMS/Studio • 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