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IQVIA

Runs drug trials and sells health data to pharma

Contract Negotiator

Contract ManagementConfirmed live in the last 24 hours
Full-timeDurham, NC, USAIn-person

About the Job

Requirements

  • A bachelor's degree in a related field, or an equivalent combination of education, training, and experience.
  • Five years of relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/or regional experience acting as a contract negotiator.
  • Negotiating and communication skills, with the ability to challenge.
  • Interpersonal skills and the ability to work as part of a team.
  • Legal, financial, and/or technical writing skills.
  • Understanding of the regulated clinical trial environment and the drug development process.
  • Knowledge of and ability to apply Good Clinical Practice, International Council for Harmonisation guidelines, and applicable regulatory guidelines.
  • Knowledge of applicable regulatory requirements, standard operating procedures, and company corporate standards.
  • Ability to exercise independent judgment and take calculated risks when making decisions.
  • Ability to lead, motivate, coach, and mentor.
  • Organizational and planning skills.
  • Presentation skills.
  • Knowledge of Microsoft Office and email applications.
  • Understanding of clinical trial contract management.
  • Ability to work within a matrix team environment.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and sponsors.
  • Ability to develop and suggest alternate contracting language, terms, and financial options.
  • Understanding of particular sponsor or stakeholder needs and ability to share this knowledge effectively with others.
  • Ability to use metrics and communicate them with the study team to establish timelines for deliverables.

Responsibilities

  • Develop global contracting strategy and support delivery of required start-up contracting activities for selected sponsors, studies, or multi-protocol programs according to sponsor requirements.
  • Develop and coordinate investigator grants and estimates, contracting strategies, and proposal text to support proposal development.
  • Develop contract language, payment language, and budget templates as required.
  • Use and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies, or multi-protocol programs in accordance with the scope of work, project plan, and agreed project strategy.
  • Collaborate and communicate with sponsors, stakeholders, and applicable RSU regions and countries to 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 study teams, as applicable to site agreements, to facilitate business development and the initiation and maintenance of clinical trials while enabling regulatory compliance.
  • Assist with creating and/or reviewing core scientific, technical, and administrative documentation to support business development and study initiation and maintenance.
  • Contribute to collecting, interpreting, analyzing, and disseminating contracting intelligence to support assigned studies and the wider company.
  • Ensure 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, including delivering training materials as required.
  • Deliver presentations to clients as required.
  • Complete and maintain internal systems, with emphasis on the Clinical Trial Management System, databases, tracking tools, timelines, and project plans accurately.
  • Proactively develop long-standing relationships with preferred IQVIA clients or customers, as applicable.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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