Full-Time

Contract Negotiator

Fsp

Posted on 4/16/2025

IQVIA

IQVIA

10,001+ employees

Analytics and research for life sciences

No salary listed

Senior

Company Historically Provides H1B Sponsorship

London, UK

Category
Contract Management
Legal & Compliance
Required Skills
Google Cloud Platform
Requirements
  • Bachelor's Degree Related field
  • 5-year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/or regional experience acting as a contract negotiator
  • Good negotiating and communication skills with ability to challenge
  • Good interpersonal skills and a strong team player
  • Strong legal, financial and/or technical writing skills
  • Strong understanding of regulated clinical trial environment and knowledge of drug development process
  • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
  • Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards
  • Ability to exercise independent judgment, taking calculated risks when making decisions
  • Ability to lead, motivate, coach and mentor
  • Good organizational and planning skills
  • Good presentation skills
  • Strong knowledge of Microsoft Office and e-mail applications
  • Good understanding of clinical trial contract management
  • Ability to work well within a matrix team environment
  • Ability to establish and maintain effective working relationships with co-workers, managers and sponsors
  • Ability to develop and suggest alternate contracting language, terms, and financial options
  • Strong understanding of particular Sponsor or stakeholder need and ability to share this knowledge effectively with others
  • Ability to utilize metrics and then communicate these with study team to establish timelines for deliverables
Responsibilities
  • Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process
  • Develop contract language, payment language and budget templates as required as applicable to the position
  • Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy
  • Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan
  • Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements
  • Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required
  • Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required
  • Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements
  • Report contracting performance metrics and out of scope contracting activities as required
  • Work with Quality Management to ensure appropriate contract management and quality standards
  • Mentor and coach colleagues as required including the delivery of training materials as required
  • Deliver presentations to clients as required
  • Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans
  • May take a proactive role in developing long standing relationships with preferred IQVIA clients/customers

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their main product, IQVIA Connected Intelligence™, utilizes big data and technology to offer insights that help clients speed up the development and marketing of new medical treatments. This system connects various healthcare data points to provide a comprehensive view of patient needs and treatment effectiveness. Unlike many competitors, IQVIA places a strong emphasis on patient privacy, using advanced technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in their efforts to understand diseases and improve treatment options.

Company Size

10,001+

Company Stage

IPO

Headquarters

Durham, North Carolina

Founded

1998

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Simplify's Take

What believers are saying

  • AI-driven patient engagement tools improve healthcare experiences and outcomes.
  • Blockchain in clinical trials enhances data security and transparency.
  • Real-world evidence use in regulatory submissions boosts demand for IQVIA's analytics services.

What critics are saying

  • Competition from AI-driven solutions by companies like Nvidia may impact market share.
  • Rapid medical innovation may strain IQVIA's resources for timely guidance.
  • Med-R1 8B adoption may face challenges against larger competitor models.

What makes IQVIA unique

  • IQVIA's Med-R1 8B LLM outperforms larger models in medical reasoning tasks.
  • Site Lab Navigator automates lab workflows, enhancing clinical trial efficiency.
  • IQVIA's AI Assistant won the 2024 PM360 Innovation Award for AI.

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Benefits

Health Insurance

Dental Insurance

Life Insurance

Flexible Work Hours

Paid Vacation

Wellness Program

401(k) Retirement Plan

Company News

BioPharmaTrend
Apr 7th, 2025
IQVIA Introduces a Compact Medical Reasoning LLM Outscoring Larger Models

IQVIA has launched Med-R1 8B, a medical reasoning large language model (LLM) designed to assist healthcare professionals in interpreting complex clinical data and scientific literature.

PR Newswire
Mar 26th, 2025
'Business Of Life Sciences And Healthcare For Leaders' Forthcoming From Umd Smith Executive Education

COLLEGE PARK, Md., March 26, 2025 /PRNewswire/ -- Registration is open for "Business of Life Sciences and Healthcare for Leaders" (B-LSHC) — an immersive five-day program focused on leadership development and honing critical-thinking and problem-solving skills in medical product development presented by Smith Executive Education at the University of Maryland's Robert H. Smith School of Business.The in-person program takes place June 23-27, 2025, at Van Munching Hall on UMD's College Park campus and is designed for mid-to-advanced career professionals in the LSHC ecosystem including pharmaceutical, biotech and medical device industries; health policy; patient advocacy; regulators; investors; and leaders across medical and regulatory fields.Program sessions will begin at 8:30 a.m. each day "and end with a luminary keynote speaker who will inspire and challenge participants to think outside the box toward the goals of creating innovative solutions for some of our most challenging problems in the LSHC ecosystem," says Wendy Sanhai, PhD, professor of the practice in management and organization for the Smith School and one of the workshop's organizers.Participants will learn from world-renowned faculty, regulatory experts and industry leaders on how to make informed decisions at crucial stages of medical product (drugs, biologics and medical devices) development – from R&D and regulatory submission to commercial launch and reimbursement. And, through expert-led sessions, dynamic capstone project discussions and case-study analysis, participants will sharpen their problem-solving and critical-thinking skills as they expand their professional network.Instructors, in addition to Sanhai, will include UMD and Smith faculty experts Balaji Padmanabhan, director of Smith's Center for Artificial Intelligence in Business; management and organization professors Jennifer Carson Marr, Oliver Schlake and Subra Tangirala; marketing professor Judy Frels; School of Public Health Dean Boris Lushniak; and School of Pharmacy Professor Joga Gobburu.The UMD experts will be joined by leading industry experts including former CEO of Scorpion Therapeutics Axel Hoos, IntoValue CEO Marion Couch, Deloitte Principals Juergen Klenk, Candy Lurken and Mathias Cousin; Euclidean Life Science Advisors President Kenneth Moch; Licensing IP negotiator Steve Ferguson; leaders from IQVIA and former FDA leaders.Participants will:Sharpen problem-solving, leadership and critical-thinking skillsCultivate holistic thinking and multidisciplinary approaches for real-world problems in the LSHC ecosystemBuild upon lessons learned and best practices from regulatory experts, industry luminaries and academic leadersExpand their professional networkIdentify major milestones, potential challenges, risks and mitigation strategies across medical product development pathways in R&D, regulatory submission, product launch and commercializationExecute critical steps in license negotiations and technology transfer processesParticipants should have at least a bachelor's degree and five years of working experience in any LSHC field.Scholarships are available, including for nonprofits, government professionals and veterans. Discounts are available for organizations with multiple participants. Information sessions via Zoom are set for 1-2 p.m

HR Tech Wire
Mar 10th, 2025
IQVIA recognized as a leader in IDC MarketScape's 2024 assessment for decentralized clinical trial technologies and consulting services

IQVIA (NYSE:IQV), a leading global provider of AI-powered analytics, technology solutions and clinical research services to the healthcare and life sciences industries, has been named to the "Leaders" category of the IDC MarketScape: Worldwide Life Science R&D Decentralized Clinical Trial Technology Solutions and Consulting Services 2024 Vendor Assessment.

Life Sciences British Columbia
Mar 4th, 2025
IQVIA Laboratories Launches Site Lab Navigator with Breakthrough e-Requisition Innovation to Transform Clinical Trials

IQVIA Laboratories launches Site Lab Navigator with breakthrough e-Requisition innovation to transform clinical trials.

IQVIA
Mar 4th, 2025
IQVIA Laboratories launches Site Lab Navigator with breakthrough e-Requisition innovation to transform clinical trials

RESEARCH TRIANGLE PARK, N.C. - March 4, 2025 - IQVIA Laboratories, a leading global drug discovery and development laboratory services organization, announces the launch of Site Lab Navigator, an advanced suite of solutions that automates and streamlines lab workflows for clinical trial sponsors and investigator sites.

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