[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