Investigator Contracts Lead – Contract Analyst II

ICON plc

Contract Analyst II managing clinical trial agreements for ICON, a global healthcare intelligence organisation. Responsibilities include negotiating terms, collaborating with teams, and ensuring compliance.

Posted 6/11/2026full-timeRemote • 🇨🇦 CanadaSeniorWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

contract managementcontract administrationcontract negotiationcontract analysisregulatory compliancelegal terminologycontract interpretationdispute resolutionclinical trial activitiesvendor agreements

Soft Skills

analytical skillsproblem-solving skillsattention to detailorganizational skillscollaborationcommunication skillstime managementprioritizationstrategic thinkingrisk assessment

Tools & Technologies

contract management systems

Industry Keywords

pharmaceutical industryclinical researchregulatory requirementsstakeholder managementcross-functional teamsmilestonesdeliverablesvendor relationshipsbusiness degreelife sciences

About the role

Key responsibilities & impact

You will take responsibility for contract management deliverables, applying your skills to ensure quality and efficiency.
Reviewing and analyzing contracts, agreements, and legal documents related to clinical trial activities and vendor relationships.
Negotiating contract terms and conditions with clients, vendors, and other stakeholders to ensure compliance with regulatory requirements and company policies.
Collaborating with cross-functional teams to assess contract risks, identify opportunities for improvement, and develop strategies to mitigate potential issues.
Maintaining accurate and up-to-date records of contract status, milestones, and deliverables using contract management systems.
Providing guidance and support to internal teams on contract-related matters, including contract interpretation, compliance, and dispute resolution.

Requirements

What you’ll need

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, preferably 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.
Willingness to travel as required (approximately 5%)

Benefits

Comp & perks

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