[Remote] Sr. Clinical Project Manager, IQVIA Biotech

Note: The job is a remote job and is open to candidates in USA. IQVIA Biotech is seeking a Sr. Clinical Project Manager to lead the delivery of clinical trials in the therapeutics of Cardiovascular, Renal, and Metabolic. This role is responsible for end-to-end clinical study execution, ensuring projects are delivered on time, within scope, and on budget, while maintaining the highest standards of quality and compliance.

Responsibilities

• Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standards
• Develop and implement integrated study management plans, ensuring consistency in processes, tools, and training
• Serve as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverables
• Set direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestones
• Partner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicable
• Proactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plans
• Collaborate with internal functional groups to support study execution and overcome operational challenges
• Monitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholders
• Ensure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate delivery
• Manage scope changes and oversee change control processes in collaboration with stakeholders
• Promote continuous improvement by sharing lessons learned and best practices
• Mentor and support the development of junior team members and contribute feedback on team performance

Skills

• Bachelor's Degree in Life Sciences or a related field required
• Greater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experience
• Proven ability to manage complex, global clinical trials and cross-functional teams
• Strong leadership, communication, and stakeholder management skills
• Demonstrated ability to manage budgets, timelines, and risk proactively
• Advanced degree preferred
• Experience leading bid defenses and client engagements is preferred

Benefits

• Incentive plans, bonuses, and/or other forms of compensation
• A range of health and welfare and/or other benefits

Company Overview

Company H1B Sponsorship