Lead Content Steward

Job not on LinkedIn

🔥 1 minute ago

🌐 United States, Canada – Remote

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🔔 Pennsylvania – Remote

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⏰ Full Time

🟠 Senior

👨🏼‍💻 Content Manager

👻 Ghost score 10%

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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

• Lead or support cross-functional groups in identifying business requirements for content modelling and reuse • Navigate changing external and internal environments and lead others through change • Implement R&D’s partnership strategy • Assist with training staff to optimally use technologies • Develop, motivate, and guide teams to success • Work across functions, regions, and cultures in a sponsor-dedicated model • Contribute to the development of treatments that benefit patients worldwide

🎯 Requirements

• Comprehensive understanding of the pharmaceutical industry, including clinical development and the prescription drug distribution process • Familiarity with document types used in drug development, including Clinical Protocols, Clinical Study Reports, Investigator Brochures, and Submission Documents • Experience with document development and understanding of the roles of different functions in developing documents • Extensive experience with MS Word • Familiarity with industry standards related to document content • Previous experience with SCM tools is helpful but not required • Demonstrated ability to work across functions, regions, and cultures • Functional-level leadership ability to inspire, motivate, and drive results • Excellent verbal and written communication skills • Ability to distill complex issues and ideas into simple, comprehensible terms • Effective team-player skills and ability to engender credibility and confidence • Ability to work in a global ecosystem with a high degree of complexity • Bachelor’s degree or related experience is required • 4+ years of experience as a medical writer or editor in the pharmaceutical industry or equivalent experience • Experience with a variety of software • Familiarity with basic concepts of information storage and retrieval • Strong attention to detail • Demonstrated ability to lead teams and work groups • Ability to work independently, take initiative, complete tasks, and meet deadlines • Strong negotiation skills • Experience with Microsoft Office applications and high-level expertise with MS Word • Familiarity with GCP and ICH standards and guidelines • 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

Apply Now

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