Site Contract Manager

IQVIA; Durham (NC); On-site; USD 49,000 - 157,000; Full time

Job summary

IQVIA is seeking a Site Contract Manager in Durham, NC to develop and coordinate global contracting strategies for clinical trials. You will craft contracts, budgets, and payment language while ensuring compliance and timely delivery across sponsors and sites.

Responsibilities include supporting study teams, managing CTMS data, and mentoring colleagues. Strong negotiation, regulatory knowledge, and MS Office proficiency are essential.

Qualifications

• Bachelor's Degree in a related field is required.
• 2+ years of sponsor or CRO site contracting experience, global or regional.
• Strong negotiation and communication skills with ability to challenge.
• Good organizational skills and knowledge of regulatory guidelines.

Responsibilities

• Develop contracting strategies and draft proposal text for studies.
• Prepare contract, payment language and budget templates.
• Maintain CTMS and project tracking for site agreements.
• Provide contracting support to study teams and sponsor interfaces.
• Mentor colleagues and contribute to training materials.

Skills

Negotiation

Communication

Teamwork

Regulatory understanding

Writing skills

Education

Bachelor's degree

Tools

Microsoft Office

Job description

## Site Contract ManagerApplylocations: Durham, North Carolina, United States of Americatime type: Full timeposted on: Posted Todayjob requisition id: R1559979**Job Overview:**Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements.**Essential Functions:*** 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. As applicable, eEnsure 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.Qualifications* Bachelor's Degree Related field Req* 2+ year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/ore regional experience acting as a contract negotiator. Equivalent combination of education, training and experience.* 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.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $49,200.00 - $157,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.