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Site Contracts Negotiator II

ICON plc

Blue Bell, PA; Nashville, TN; Hickory, NC; Raleigh, NC; Mt. Pleasant, SC; Bristol, TN; Cary, NC; Salisbury, NC; Wilmington, NC; Charlotte, NC; Rocky Mount, NC; Long Beach, CA; New York, NY; Rochester, NY; Knoxville, TN; Sherman Oaks, CA; San Antonio, TX; Lawrence, KS; Portland, OR; Cambridge, MA; Downers Grove, IL; Boston, MA; Piedmont, NC; McFarland, IA; Houston, TX; Lexington, KY; Whitesboro, NY; Salt Lake City, UT; Farmingdale, NYRemotePosted 4 days ago
Full TimeEntry LevelClinical DevelopmentCRO
Original posting ↗

Summary

Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites.

Job description

Role Summary

Responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites.

Responsibilities

  • Drafts, reviews, negotiates, and finalizes clinical trial agreements, complex amendments, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON's fundamental interests and is consistent with ICON's rules, procedures, and policies.
  • Maintains consistent communication with study sites and internal stakeholders in alignment with site contracts department and client requirements.
  • Tracks progress of site contracts agreements and related documents regularly in required ICON and client systems.
  • Proactively identifies and raises risks, while also suggesting mitigation plans to established study milestones and planned site contracts timelines.
  • Files contractual documents as per department, ICON, and client requirements.
  • Attends and participates in study team project calls, as applicable.
  • Works cross functionally with internal stakeholders in support of timely site start up and maintenance for the conduct of clinical trials including accurate forecast of contract execution timelines.
  • Reviews site contracts for completeness and accuracy and ensures adherence to department and client requirements, corrects documents, and files changes to contracts.
  • Completes all required project, client, department, and ICON trainings on time and adheres to the applicable SOPs, processes and procedures.

What you need

  • Bachelor's Degree
  • 0-3 years of experience in a Clinical Research environment
  • Demonstrates professionalism in conducting daily activities.
  • Exhibits extensive competency in Microsoft Office Suite applications (i.e. Word, Excel, PowerPoint, Outlook).
  • Ability to follow written and oral instructions from a variety of sources.
  • Completes tasks independently on time and in an efficient manner.
  • Ability to mentor and train other site contracts team members as needed.
  • Demonstrates effective time management skills and has ability to prioritize multiple tasks with management guidance and oversight.
  • Strong attention to detail.
  • Great interpersonal and communication skills.
  • Confidence in dealing with external and internal clients.

Requirements

  • Bachelor's Degree
  • 0-3 years of experience in a Clinical Research environment
  • Demonstrates professionalism in conducting daily activities
  • Exhibits extensive competency in Microsoft Office Suite applications (Word, Excel, PowerPoint, Outlook)
  • Ability to follow written and oral instructions from a variety of sources
  • Completes tasks independently on time and in an efficient manner
  • Ability to mentor and train other site contracts team members as needed
  • Demonstrates effective time management skills and ability to prioritize multiple tasks
  • Strong attention to detail
  • Great interpersonal and communication skills
  • Confidence in dealing with external and internal clients

Benefits

  • Competitive base salary
  • Performance related incentives
  • Medical, Dental & Vision
  • Retirement & Pension Plans
  • Life Assurance
  • Disability Coverage
  • Employee Assistance Programmes
  • Wellbeing Resources
  • Learning & Development Opportunities

Company overview

ICON plc is a global leader in clinical research and healthcare intelligence, founded in Dublin, Ireland in 1990. As one of the world's largest contract research organizations (CROs), ICON provides comprehensive outsourced development services to pharmaceutical, biotechnology, and medical device companies worldwide. The company operates in 55 countries with approximately 41,900 employees, offering end-to-end solutions that span the entire product development lifecycle. ICON's service portfolio includes clinical research services, adaptive trials, biosimilars, commercialization and outcomes consulting, medical imaging, laboratory services, and strategic support for traditional and digital health technologies. The company specializes in therapeutic areas such as oncology, cardiovascular diseases, central nervous system disorders, rare diseases, and women's health. With its 2021 acquisition of PRA Health Sciences, ICON significantly expanded its capabilities and market position, becoming a dominant force in the global CRO industry. The company is publicly traded on NASDAQ under the ticker ICLR and reported $8.28 billion in revenue for 2024.

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