Contract Specialist for the site activation team
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Job Summary
Job Overview
Under general supervision perform tasks at a country level associated with site activation activities in accordance withapplicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines.
The Contract Specialist is responsible for independently managing the preparation review and negotiation of clinical site agreements in support of study start-up activities. This role contributes directly to achieving study timelines by ensuring efficient contract execution while maintaining compliance with applicable regulations sponsor requirements and internal policies.
Essential Functions
Independently draft review and negotiate standard clinical trial agreements (e.g. CTAs CDAs amendments) with investigative sites and institutions.
Manage assigned contract portfolio to support site activation deliverables and study timelines.
Act as a primary point of contact for sites and internal teams for contract-related matters ensuring clear and timely communication.
Apply approved negotiation parameters and escalate non-standard terms or higher-risk issues to senior team members or Legal as needed.
Collaborate with cross-functional stakeholders (e.g. Site Activation Clinical Operations Finance) to align contract terms including budget-related provisions.
Track contract progress and maintain accurate up-to-date documentation in relevant systems and tools.
Identify and proactively address contract-related delays working to resolve issues and minimize impact on study timelines.
Ensure all contracts comply with applicable regulatory requirements sponsor guidelines and company policies.
Support audit and inspection readiness by maintaining complete and accurate contract files.
Contribute to continuous process improvements aimed at enhancing contract cycle times and quality.
Manage multiple priorities simultaneously while meeting established timelines and quality expectations.
Provide regular status updates and metrics to stakeholders and project teams.
Qualifications
Bachelors degree
At least 2 years of experience in a CRO or pharma supporting the contract and budget negotiation with sites.
Advanced level of English skills
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
IQVIA 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.
Required Experience:
IC
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
