Clinical Project Manager

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

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

• Leading and coordinate project activities, ensuring that projects are delivered on time, within budget, and to the highest quality standards • Coordinating project and program management delivery, resolving issues, and developing team capability in a sponsor-dedicated model environment • Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery • Leading cross-functional project teams, coordinating efforts to meet project objectives, and facilitating effective communication and collaboration • Monitoring project progress, identifying potential risks and issues, and implementing strategies to address challenges and keep projects on track • Engaging with stakeholders to manage expectations, provide updates, and ensure alignment with project goals and organizational objectives • Preparing and presenting project reports, status updates, and performance metrics to senior management and other stakeholders

🎯 Requirements

• Bachelor's degree in life sciences or related discipline • At least 7 + years of relevant study management experience in a pharmaceutical/scientific environment • Strong skills and experience in project management and tools • In-depth knowledge of GCPs and ICH guidelines • In-depth experience in clinical research: study management, monitoring, data management • Strong performer / executor of operational tasks with strong skills and experience in study delivery • Experience of working across multiple types of study designs • Demonstrates leadership skills, promoting motivation and empowerment of others in order to accomplish individual, team and organizational objectives • Proven track record of successfully managing projects from inception to completion, with a focus on delivering results within scope, time, and budget constraints • Excellent communication and interpersonal skills, with the ability to build relationships and manage stakeholder expectations • Proficiency in project management tools and methodologies, with certifications such as PMP or PRINCE2 being advantageous

🏖️ 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