Clinical Program Manager

IQVIA LLC; Durham (NC); On-site; USD 93,000 - 286,000; Full time

Job summary

IQVIA is seeking Senior Project Leaders/Clinical Program Managers to join a sponsor-dedicated unit. You will liaise between IQVIA/sponsor functions and customers, owning delivery quality and financial control across global cross-functional teams, supported by domain experts.

MSP expertise and strong analytics are essential for study/program timelines. You will work with Clinical Leads, Vendor Managers, and activation managers to drive governance, risk mitigation, and budget management on one or

Qualifications

• Bachelor's Degree required; PMI/PMI-ACP or similar certification preferred.
• Minimum 5 years of Clinical Project Management experience in industry/CRO/business.
• Proficient in MS Project and strong governance mindset.

Responsibilities

• Leading global cross-functional project team delivery.
• Accountable for milestones, quality, and contracted scope.
• Primary customer contact for progress and governance.
• Developing study management plans and ensuring tool usage and compliance.
• Anticipating risk and implementing mitigation strategies.
• Managing study team assignments, accountability and resources.
• Ensuring study budget is managed, including scope changes and financial systems accuracy.

Skills

Cross-functional leadership

Conflict resolution

Governance management

Analytical ability

Education

Bachelor's degree

Professional Project Management certification

Tools

MS Project

Job description

Job Summary: We are looking for Senior Project Leaders/Clinical Program Managers to join our innovative and dynamic group of global professionals dedicated to assisting our clients in driving healthcare forward. This is an important and high-profile role within our sponsor-dedicated business unit to enable medical breakthroughs that advance healthcare and patient treatment options around the world. As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will manage cross functional teams across this global organization and be supported by domain experts in every function, enabled by best-in-class technology and data analytics. This role owns study and or program level timelines and planning; Microsoft Project (MSP) expertise is a must-have, as well as developed analytic skills. Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager an expert in start-up. IQVIA’s size and global footprint will present you with the breadth of opportunities necessary to develop your career. Typically assigned to one or two projects, or a program.

Responsibilities

• Leading global cross-functional project team delivery
• accountable for achievement of milestones and quality of contracted scope
• Serving as the primary contact with the customer for progress and governance
• Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures
• Anticipating risk and implementing mitigation strategies
• Managing study team assignments, accountability and resource requirements
• Ensuring the study budget is managed proactively including scope changes and financial systems are accurate

Requirements

• Bachelors Degree Professional Project Management certification is preferred
• A minimum of 5 years’ in Clinical Project Management in industry/CRO/business experience is required in clinical drug development and/or clinical operations, clinical R&D experience preferred.
• Prior experience leading a cross-functional global teams is required
• Demonstrated ability to resolve conflict and influence teams without direct authority
• Successful experience in planning and management of governance bodies is preferred
• Proficient in MS Project is required

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.

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.

The potential base pay range for this role, when annualized, is $93,100.00 - $285,500.00. 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).

• 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.

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.

Everything we do is part of a journey to 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.

Thank you for your interest in growing your career with us.