Senior Study Delivery Lead

🔥 1 hour ago

🌐 United Kingdom, Romania, +3 more countries – Remote

🇬🇧 United Kingdom – Remote 🇷🇴 Romania – Remote 🇪🇸 Spain – Remote 🇵🇱 Poland – Remote 🇧🇬 Bulgaria – Remote

⏰ Full Time

🟠 Senior

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.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

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

• Lead and coordinate project activities • Oversee project execution, including planning, resource management, stakeholder communication, and risk mitigation • Design, execute, and report clinical studies and trials • Plan and lead delivery of non-interventional studies to time, quality, budget, company standards, and scientific requirements from concept protocol to final study report • Coordinate and deliver feasible Study Protocols, Informed Consent Forms, operationally robust study documents, and Clinical Study Reports • Develop study delivery strategies, including country selection, diversity, patient identification and engagement, recruitment plans, and digital platforms/tools • Assess, select, engage, and manage appropriate vendors • Ensure compliance with ICH/GCP, ENCePP, and applicable study guidelines • Make risk-benefit decisions and mitigate risks • Develop and manage study-level budgets within project budget allocations • Build partnerships and collaborate with therapy-aligned staff and global functions • Lead study teams with single-point accountability for study delivery • Serve as a focal point for interactions with lead scientists, data management, biostatistics, legal, compliance, and project management stakeholders

🎯 Requirements

• Ideally, you will be a Project Manager or experienced Senior Clinical Trial Manager with retrospective and prospective designs, post authorization safety studies, real world evidence, and epidemiology experience • Global clinical study management experience across different countries and regions • Proven expertise in the proactive identification of issues which may impact clinical programmes coupled with the ability to contribute to solutions affecting cross-functional matrix teams • Advanced degree (e.g. MS, PhD, PharmD) or equivalent experience • Demonstrated experience leading in matrix environment to deliver projects, develop clinical plans, and manage change • Ability to work independently and proactively and to take on leadership roles on cross-functional study teams • Excellent leadership, influencing and negotiation skills • Ability to lead and drive change, continuous improvement and learning, effectiveness at building networks of partners and stakeholders • A minimum ideally of 6+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization • Bachelor's degree in health, life sciences, or Advanced degree (e.g. MS, PhD, PharmD) • Ideally, at least 10+ years of relevant experience in clinical trial management • Experience in managing complex or global trials is advantageous • Preferred: Experience in managing all trial components from start-up to database lock • Preferred: Experience in leading and driving cross-functional teams including oversight of external CROs, etc. • 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

📊 Check your resume score for this job

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

Upload Resume