Director, Clinical Research Scientist

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🔥 0 minutes ago

🌲 North Carolina, Pennsylvania – Remote

🌲 North Carolina – Remote 🔔 Pennsylvania – Remote

⏰ Full Time

🔴 Lead

🧪 Clinical Research

👻 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

• Develop protocols for clinical studies • Contribute to program strategy for assigned compounds/programs, including preparation of clinical development plans • Draft clinical scientific documents such as INDs, IND amendments, Clinical Study Reports, Investigator Brochures, Annual Reports, and other health authority submissions • Provide clinical input into eCRF design, SAP, and TLFs • Monitor, review, and summarize clinical safety and efficacy data in ongoing studies • Review study data to identify and evaluate data trends • Lead clinical matrix teams for assigned studies and represent clinical development on project teams • Serve as liaison to project teams, CROs, and other stakeholders • Provide clinical updates to senior management, project teams, steering committees, clinical sub-teams, governance meetings, eDMC meetings, advocacy groups, scientific advisory boards, and publications committees • Liaise with cross-functional teams on training, study results, and meetings with lead PIs/KOLs at conferences; present as needed • Develop relationships with consultants and external experts to obtain protocol design feedback • Contribute to writing and reviewing study abstracts, posters, oral presentations, and manuscripts

🎯 Requirements

• Degree in scientific /life-sciences field • Pharm.D. or Ph.D. preferred • Minimum of 4 - 6 years of experience in research with at least 3 or more years of clinical research/drug development experience are required for Director level • Experience in Immunology field is required • Ability to multi-task and work in a fast-paced environment • Excellent written and oral communication skills • Strong Analytical ability • Ability to accommodate up to 20% travel or as business dictates • 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