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Contract Analyst I

  • Blue Bell, Pennsylvania, United States
  • Remote
  • Posted Oct 5, 2026
  • 1 position

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Employment type
Full-time
Experience level
Mid-level · 2+ years
Minimum education
Bachelor’s degree
Posting language
English
Working hours
40 hours per week

Job summary

You will manage contract activities including negotiating clinical trial agreements, budgets, and payment terms with assigned sites. Additionally, you will partner with internal teams to improve site activation metrics and ensure project standards are met.

Job details

Contract Analyst I ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Contract Analyst I at ICON, you will prepare, verifying, and carrying out invoicing via electronic processing and reporting activities for an assigned portfolio of accounts. What You Will Do: You will contribute to contract management activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Negotiate directly with assigned sites on all site related contracting items including clinical trial agreements, budgets, payment terms, ancillary agreements and amendments. Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes. Ensure standards are applied to the SB&C processes across projects. Leverage leading industry tools and data sources to provide budget and contract feedback aligned with parameters and fair market value guidance. Promptly recognize and improve potential delays and escalate to appropriate team members. Track all actions and negotiations to ensure timelines are achieved for studies and sites assigned. Support resolving escalated issues identified by the site activation sub-team in partnership with the internal Study Startup team. Your Profile: You will bring relevant contract management experience, along with the following qualifications and skills. Required qualifications and experience: BS degree or international equivalent 2 or more years of experience in clinical research site contracting and budgeting within a pharmaceutical company, CRO or relevant industry vendor. Ability to explain data to facilitate decision making processes to be data driven. Knowledge and understanding of clinical study protocols and schedule of assessments Strong organizational skills, decision making, communication and negotiation skills. Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: 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 Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply

What you’ll do

You will manage contract activities including negotiating clinical trial agreements, budgets, and payment terms with assigned sites. Additionally, you will partner with internal teams to improve site activation metrics and ensure project standards are met.

Requirements

Candidates must hold a bachelor degree or international equivalent and possess at least 2 years of experience in clinical research site contracting and budgeting. Strong negotiation, communication, and organizational skills are required to succeed in this role.

Benefits

  • Competitive base salary
  • Performance related incentives
  • Medical coverage
  • Dental coverage
  • Vision coverage
  • Retirement plans
  • Pension plans
  • Life assurance
  • Disability coverage
  • Employee assistance programmes
  • Wellbeing resources
  • Learning and development opportunities

Listed skills

  • Budgeting · Preferred
  • Data analysis · Preferred
  • Decision Making · Preferred
  • Negotiation · Preferred
  • Communication · Preferred
  • Reporting · Preferred
  • invoicing · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

  • Contract management
  • Clinical research
  • Budgeting
  • Negotiation
  • Clinical trial agreements
  • Data analysis
  • Communication
  • Organizational skills
  • Decision making
  • Clinical study protocols
  • Schedule of assessments
  • Invoicing
  • Reporting
  • Site activation
  • Organizational Skills
  • Decision Making
  • Clinical Research
  • Clinical Trials
  • Contract Management
  • Market Value
  • Operations
  • Pharmaceuticals
  • Timelines

Job areas

  • Healthcare
  • Science & Research
  • Finance & Accounting
  • Legal
  • Administrative
  • Contract Analyst
  • Contracts Analyst
  • Buyers
  • Purchasing Agents, Except Wholesale, Retail, and Farm Products
  • Buyers and Purchasing Agents

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