Project Manager

🔥 19 hours ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 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

• Support vendor procurement, contracting and purchase order processes • Assist with study budgets, study set-up and oversight documentation • Coordinate study documentation, action trackers and meeting minutes • Support study team and country-level communications • Liaise between internal study teams and CRO project managers • Maintain study documentation, risk logs and tracking tools • Coordinate cross-functional meetings and stakeholder communications • Support study registration, site contracting and ethics approval processes • Assist with advisory board and steering committee meeting preparation and documentation • Provide support for investigator contracting, payments and study systems • Support study closure activities, including system close-out, archiving and final document management • Support delivery of complex global oncology clinical studies from start-up through close-out

🎯 Requirements

• Bachelor's degree in a scientific or life sciences discipline • Strong experience working within the pharmaceutical, biotechnology, CRO or clinical research industry in an Oncology project management role • Home-based already residing in the UK • Experience of Phase IV and/or Real World Evidence trials in a trial management capacity • Proven ability to manage multiple priorities and projects simultaneously • Strong organisational, stakeholder management and communication skills • Experience working within cross-functional, matrix environments • 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