
10,000+ employees
đŒ Consulting
đ Manufacturing
đŁ Marketing
đ° $1G Post-IPO Debt on 2023-05
Consulting âą Manufacturing âą Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
đ„ 12 hours ago
Improve your chances of getting an interview by checking your resume score before you apply.

10,000+ employees
đŒ Consulting
đ Manufacturing
đŁ Marketing
đ° $1G Post-IPO Debt on 2023-05
Consulting âą Manufacturing âą Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
âą Draft, review, and negotiate standard clinical trial agreements, including CTAs, CDAs, and amendments âą Manage assigned contract portfolio to support site activation deliverables and study timelines âą Serve as primary point of contact for sites and internal teams on contract-related matters âą Apply approved negotiation parameters and escalate non-standard terms or higher-risk issues âą Collaborate with Site Activation, Clinical Operations, and Finance stakeholders on contract terms and budget provisions âą Track contract progress and maintain accurate documentation in relevant systems âą Identify and resolve contract-related delays to minimize impact on study timelines âą Ensure contracts comply with regulatory requirements, sponsor guidelines, and company policies âą Maintain complete and accurate contract files for audit and inspection readiness âą Contribute to process improvements enhancing contract cycle times and quality âą Manage multiple priorities while meeting timelines and quality expectations âą Provide status updates and metrics to stakeholders and project teams
âą Based in Brazil or Argentina âą Bachelor's degree âą 2 to 4 years of experience in clinical research (CRO or pharma) supporting contract and budget negotiation with sites, including direct contract/budget negotiation experience âą Advanced level of English skills âą Ability to submit CV in English
âą Home based role âą Full-time employment
Apply Now