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Site Budget Specialist
hace 2 meses
About the Role
IQVIA Argentina is seeking a highly skilled Site Budget Specialist to join our team. As a Site Budget Specialist, you will be responsible for providing a suite of Site Budget and Contracts Services to our clients. This role will involve participating on project teams to deliver Site Budget and Contracts Services to clients on time, within budget, and in accordance with applicable financial, contractual, and pharmaceutical R&D industry standards and regulations.
Key Responsibilities
- Client Liaison
Serve as the primary point of contact for clients using a single Site Budget and Contracts service for US and Canada.
Project LeadershipLead internal project kick-off meetings for single solution engagements, including a review of the Statement of Work (SoW) and the service delivery model.
Contract PreparationPrepare Disclosure Agreements (CDAs), Clinical Trial Agreements (CTAs), and other related contractual documents based on client-approved templates.
Negotiation and EscalationNegotiate contractual documents using established negotiation and escalation plans.
Service DeliveryTrack the delivery of services against the SoW and ensure that agreed-upon project targets and milestones are achieved.
Project OversightLead client-specific or departmental projects, overseeing other Site Budget and Contracts staff to ensure timely delivery.
Performance ManagementPrepare ongoing unit-based forecasts for assigned projects and measure performance against those forecasts.
Escalation PointServe as an internal escalation point for project-related issues and challenges.
Requirements
- Education
Bachelor's Degree in a related field.
Experience5 years of relevant sponsor or clinical research organization clinical site contracting experience, including global and/or regional experience as a contract negotiator.
SkillsGood negotiating and communication skills, with the ability to challenge and negotiate effectively.
Interpersonal SkillsGood interpersonal skills and a strong team player.
Writing SkillsStrong legal, financial, and/or technical writing skills.
Regulated EnvironmentStrong understanding of regulated clinical trial environments and knowledge of the drug development process.