As a DCT Study Lead (remote position), you will be at the forefront of transforming clinical research through decentralized and hybrid trial models. You will lead the strategic planning and operational execution of DCT components across global studies, ensuring seamless integration of digital health technologies, remote services, and patient-centric solutions. This role requires strong leadership, cross-functional collaboration, and a deep understanding of clinical trial delivery in a virtual or hybrid setting.

Key Responsibilities

Project Leadership & StrategyLead the end-to-end delivery of decentralized and hybrid clinical trials, ensuring alignment with contractual obligations, timelines, and quality standards.Orchestrate the project  DCT team to drive execution, accountability and continuous alignment across functions.Serve as the primary DCT contact for clients, internal teams, and vendors, providing strategic oversight and operational direction.Collaborate with traditional study teams to integrate DCT elements into broader trial frameworks.

Cross-Functional CollaborationPartner with internal stakeholders including technology integrations, mobile nursing, regulatory, site support, and data management to ensure cohesive delivery.Drive the development of integrated study management plans and ensure milestone achievement.

Risk & Quality ManagementProactively identify risks and implement mitigation strategies.Monitor quality metrics and ensure compliance with GCP, SOPs, and regulatory requirements.Apply lessons learned

Financial OversightManage project budgets, resource allocation, and financial forecasting.Identify scope changes and lead the change control process, including client negotiations.

Client Engagement & CommunicationLead client meetings, bid defenses, and DCT-specific presentations.Act as a trusted advisor to clients, offering insights on DCT strategy, innovation, and best practices.

Team Leadership & DevelopmentContribute to internal training and knowledge-sharing initiatives on DCT methodologies.

Qualifications & Skills

Bachelor’s degree in Life Sciences or related field.Minimum 3 years of experience in clinical research,Proven track record in  in project management, client engagement, and cross-functional leadership.Nice to have: Interest of  DCT technologies (e.g., eConsent, telehealth, wearables, remote monitoring).Excellent communication, negotiation, and presentation skills.Ability to navigate ambiguity rapid adjusting strategies and workflow.Proficiency in MS Office and clinical trial systems (CTMS, eTMF, etc.).Experience with DCT platform implementation or digital health tools.Financial acumen and experience managing project budgets.Ability to work across geographies and cultures.Strong problem-solving and decision-making capabilities.Highly goal-oriented upon client needs and agreementsPassion for innovation and continuous improvement in clinical trial delivery.

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.com