Note: The job is a remote job and is open to candidates in USA. IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The Senior Clinical Project Manager leads the planning, execution, and delivery of global MedTech clinical studies, managing sponsors, cross-functional teams, budgets, timelines, risks, and regulatory compliance.
Responsibilities
- Lead the planning, execution, and delivery of global and multi-country MedTech clinical studies
- Serve as the primary project contact for sponsors and maintain strong client relationships throughout the study lifecycle
- Develop and manage study timelines, budgets, forecasts, risk management plans, and project deliverables
- Lead cross-functional project teams to ensure milestones are achieved and study objectives are met
- Monitor study progress and proactively identify, escalate, and resolve project risks and issues
- Ensure compliance with ICH-GCP, ISO 14155, applicable regulatory requirements, SOPs, and quality standards
- Collaborate with Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Safety, and other functional groups to support successful study execution
- Manage study finances, including forecasting, scope management, change orders, and overall project profitability
- Support bid defenses and business development activities for new opportunities
- Drive continuous process improvement and share lessons learned and best practices across project teams
- Mentor and support the development of junior project management and clinical operations staff
- Provide regular project updates and strategic recommendations to sponsors and internal stakeholders
Skills
- Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, Public Health, Healthcare, or a related scientific discipline required
- Minimum of 7 years of clinical research experience, including at least 4 years of clinical project management experience
- Experience managing clinical studies within the MedTech, medical device, diagnostics, CRO, biotechnology, pharmaceutical, or healthcare industries
- Demonstrated experience leading global and multi-country clinical studies across North America, Europe, Asia-Pacific, and other regions
- Experience managing cross-functional project teams and complex stakeholder relationships
- Strong knowledge of clinical trial management and applicable regulations, including ICH-GCP, ISO 14155, FDA, and global regulatory requirements
- Proven ability to lead global, cross-functional teams in a matrix environment
- Excellent client relationship management, communication, presentation, and negotiation skills
- Strong project planning, organizational, and problem-solving abilities
- Demonstrated experience managing project budgets, contracts, forecasting, and financial performance
- Ability to manage multiple priorities and deliver results in a fast-paced environment
- Strong attention to detail and commitment to quality
- Advanced proficiency with Microsoft Office and clinical trial management systems
- Ability to effectively collaborate across global teams and cultures
- Demonstrated commitment to customer service, operational excellence, and continuous improvement
- Experience supporting studies intended for regulatory submissions, product development, and post-market evidence generation preferred
Benefits
- Incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to base pay.
- Health and welfare and/or other benefits may be offered.
Company Overview
Company H1B Sponsorship