Clinical Site Contracts Specialist

🔥 1 minute ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👻 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

• Review and analyze contracts, agreements, and legal documents related to clinical trial activities and vendor relationships • Negotiate contract terms and conditions with clients, vendors, and other stakeholders • Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company-sponsored and investigator-initiated studies • Negotiate directly with clinical trial sites or oversee a Clinical Research Organization responsible for contract negotiations • Work with global teams to review and analyze contractual terms and conditions • Assess legal and budget risks with team support functions • Analyze investigator fees against fair market value pricing and regional standards and J&J pricing guidelines • Support negotiations for confidentiality agreements, informed consent forms, and other ancillary contract documents • Participate in developing site/investigator budgets aligned with fair market value • Manage the contract amendment lifecycle

🎯 Requirements

• Bachelor's degree in business, life sciences, communications, or a related discipline • Minimum of 2 years of experience in contract administration, contract management, or a related field, in the pharmaceutical or clinical research industry • Strong understanding of contract law, legal terminology, and regulatory requirements related to clinical trials and vendor agreements • Excellent analytical and problem-solving skills, with the ability to evaluate complex contractual issues and propose effective solutions • Strong attention to detail and organizational skills, with the ability to manage multiple tasks and prioritize work effectively in a fast-paced environment • 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