Research Associate I – Scientific Data Curation

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Logo of ICON plc

ICON plc

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

• Maintain and develop high-quality scientific content within the ePROVIDE™ platform • Curate accurate, structured scientific data across PROQOLID™, PROLABELS™, and PROINSIGHT™ • Identify, source, and screen information on clinical outcome assessments, endpoint strategies, regulatory label claims, clinical guidelines, and agency recommendations • Extract and summarise information from scientific publications, regulatory labels, Summary of Product Characteristics documents, public assessment reports, clinical guidelines, and agency-published documents • Apply database-specific rules, scope criteria, taxonomy, and quality standards to ensure scientific consistency, traceability, and data integrity • Collaborate with Database Team members and cross-functional colleagues to support client-facing and internal use of ePROVIDE™ data • Support database updates, quality checks, documentation, and continuous improvement activities

🎯 Requirements

• Bachelor’s or Master’s degree in a relevant scientific discipline, such as psychology, public health, life sciences, health sciences, pharmacy, biomedical sciences, or a related field • Previous experience in clinical research, health outcomes research, scientific literature review, data curation, or a related field • Ability to read, interpret, and summarise scientific, clinical, and regulatory information accurately • Strong attention to detail, consistency, and documentation • Ability to follow defined rules and quality standards • Flexibility to apply rules consistently while adapting scientific judgement when justified exceptions arise • Good organisational skills and ability to manage multiple curation tasks or database updates in parallel while respecting timelines • Proactive and independent, with locus of control • Strong communication and collaboration skills for a team-based, cross-functional environment • Comfort working with digital platforms, structured databases, and data extraction tools • Ability to work fully in English within an international department and team environment • 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

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