Sr. Clinical Project Manager, IQVIA Biotech

IQVIA; Durham (NC); On-site; USD 93,000 - 233,000; Full time

Benefits offered by this job

Incentive plans

Bonuses

Health and welfare benefits

Job summary

IQVIA Biotech, in Durham, NC, seeks a Senior Clinical Project Manager to lead end-to-end clinical study execution, ensuring on-time, on-scope delivery with top-quality compliance.

You will oversee cross-functional teams, manage budgets and timelines, and mentor junior staff while collaborating with sponsors on bid defenses and strategic opportunities.

Qualifications

• 7+ years of clinical research experience with at least 4 years of project management 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.
• Experience leading bid defenses and client engagements preferred.

Responsibilities

• Lead planning, execution, and delivery of medium to large, multi-regional studies in line with contracts, SOPs and regulatory standards.
• Develop and implement integrated study management plans across processes, tools, and training.
• Serve as primary liaison with sponsors, managing relationships and communicating risks and deliverables.

Skills

Leadership

Communication

Stakeholder management

Budgeting and forecasting

Timeline management

Risk management

Bid defenses / client engagements

Education

Bachelor's Degree in Life Sciences

Advanced degree preferred

Job description

Overview

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

The Senior Clinical Project Manager is a key leader in the delivery of clinical trials, partnering with cross-functional teams and clients to accelerate the development of life-changing therapies. 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. The Senior Clinical Project Manager provides strategic oversight, operational leadership, and serves as the primary point of contact for sponsors.

Key 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.

Qualifications

• Bachelor's Degree in Life Sciences or a related field required; advanced degree preferred.
• Requires 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.
• Experience leading bid defenses and client engagements is preferred.

Benefits

Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Salary

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

About IQVIA

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.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

EEO Statement

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

Legal

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Additional Information

Learn more at https://jobs.iqvia.com. Thank you for your interest in growing your career with us.