[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.ResponsibilitiesLead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standardsDevelop and implement integrated study management plans, ensuring consistency in processes, tools, and trainingServe as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverablesSet direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestonesPartner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicableProactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plansCollaborate with internal functional groups to support study execution and overcome operational challengesMonitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholdersEnsure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate deliveryManage scope changes and oversee change control processes in collaboration with stakeholdersPromote continuous improvement by sharing lessons learned and best practicesMentor and support the development of junior team members and contribute feedback on team performanceSkillsBachelor's Degree in Life Sciences or a related field requiredGreater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experienceProven ability to manage complex, global clinical trials and cross-functional teamsStrong leadership, communication, and stakeholder management skillsDemonstrated ability to manage budgets, timelines, and risk proactivelyAdvanced degree preferredExperience leading bid defenses and client engagements is preferredBenefitsIncentive plans, bonuses, and/or other forms of compensationA range of health and welfare and/or other benefitsCompany OverviewIQVIA provides analytics, compliance, and management solutions to the life sciences industry. It was founded in 1982, and is headquartered in Danbury, Connecticut, USA, with a workforce of 10001+ employees. Its website is https://www.iqvia.com.Company H1B SponsorshipIQVIA has a track record of offering H1B sponsorships, with 44 in 2026, 167 in 2025, 290 in 2024, 258 in 2023, 229 in 2022, 208 in 2021, 180 in 2020. Please note that this does not guarantee sponsorship for this specific role.