Clinical Research Coordinator – Pre-clinical

Job not on LinkedIn

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Co-ordinate the outsourcing and delivery of preclinical CPSS project activities • Support the development, maintenance, and interpretation of cross-functional project plans • Monitor timelines, budgets, resources, risks, and project deliverables • Facilitate communication and collaboration across project teams and stakeholders • Support management of external vendors and outsourced activities • Provide guidance on project management processes, tools, and best practices • Identify and help resolve day-to-day project challenges and risks • Communicate new processes, procedures, and strategies to project teams • Contribute to continuous improvement initiatives to enhance project delivery, quality, and efficiency

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline • Experience in Scientific Project Management • Experience supporting pre-clinical drug development projects and activities • Strong organisational, planning, and communication skills • Ability to manage multiple priorities and work effectively within cross-functional teams • Understanding of scientific project management principles, including project planning, resource management, and risk management • Advanced degree in a relevant scientific field (desirable) • Experience within a pharmaceutical, biotech, or clinical research environment (desirable) • Experience in project co-ordination, project management, or change management (desirable) • Professional project management certification (PMP, PRINCE2, Agile, or equivalent) (desirable) • Broad understanding of scientific project management and drug development processes (desirable) • 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