Overview Customer dedicated Clinical Project Management Director taking an Indication Director role to provide operational delivery oversight for select indication(s). Provides strategic and ...
Overview Customer dedicated Clinical Project Management Director taking an Indication Director role to provide operational delivery oversight for select indication(s). Provides strategic and ...
The Clinical Program Manager reports to the Program Director and Clinical Operations Group Leader ... project management of clinical trials experience managing all aspects of a Clinical Project to ...
The Clinical Program Manager reports to the Program Director and Clinical Operations Group Leader ... project management of clinical trials experience managing all aspects of a Clinical Project to ...
The Clinical Program Manager reports to the Program Director and Clinical Operations Group Leader ... project management of clinical trials experience managing all aspects of a Clinical Project to ...
The Clinical Program Manager reports to the Program Director and Clinical Operations Group Leader ... project management of clinical trials experience managing all aspects of a Clinical Project to ...
Clinical Project Manager
Toledo, OH · On-site
... management position responsible for planning, coordinating, implementing, and monitoring clinical ... Support program directors with operational planning, implementation, and evaluation of program ...
Clinical Project Manager
Toledo, OH · On-site
... management position responsible for planning, coordinating, implementing, and monitoring clinical ... Support program directors with operational planning, implementation, and evaluation of program ...
Clinical Project Manager - Renal
$155K - $175K/yr
About You To be successful in this role, you will have: • 5-7 years of project management experience in clinical research, preferably in a CRO or pharmaceutical environment. • Strong Nephrology ...
Clinical Project Manager - Renal
$155K - $175K/yr
About You To be successful in this role, you will have: • 5-7 years of project management experience in clinical research, preferably in a CRO or pharmaceutical environment. • Strong Nephrology ...
Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications * Minimum of a Bachelors degree, but preferrably a Masters or PhD ...
Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications * Minimum of a Bachelors degree, but preferrably a Masters or PhD ...
Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications * Minimum of a Bachelors degree, but preferrably a Masters or PhD ...
Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications * Minimum of a Bachelors degree, but preferrably a Masters or PhD ...
Associate Director, Clinical Data Management
Bothell, WA · On-site
$190K - $205K/yr
Description ASSOCIATE DIRECTOR, CLINICAL DATA MANAGEMENT JOB SUMMARY TheAssociateDirector,Clinical ... Ensure CRO adherence to project timelines, from study startup through study closeout. * Collaborate ...
Associate Director, Clinical Data Management
Bothell, WA · On-site
$190K - $205K/yr
Description ASSOCIATE DIRECTOR, CLINICAL DATA MANAGEMENT JOB SUMMARY TheAssociateDirector,Clinical ... Ensure CRO adherence to project timelines, from study startup through study closeout. * Collaborate ...
Mark Prince, Associate Professor and Director of My Mental Health Data Analysis and Dissemination, the Clinical Project Manager will play a central role in coordinating research operations, ensuring ...
Mark Prince, Associate Professor and Director of My Mental Health Data Analysis and Dissemination, the Clinical Project Manager will play a central role in coordinating research operations, ensuring ...
Project management skills required to include the use of a formal process and system for planning and tracking ongoing progress of clinical projects * Vendor management experience required. * The ...
Project management skills required to include the use of a formal process and system for planning and tracking ongoing progress of clinical projects * Vendor management experience required. * The ...
Clinical Trial Manager
San Francisco, CA · On-site
$145K - $165K/yr
In this role, you'll take ownership of the day-to-day tactical management of ongoing studies ... This role reports to the Senior Director, Clinical Operations. Required Qualifications * Degree in ...
Clinical Trial Manager
San Francisco, CA · On-site
$145K - $165K/yr
In this role, you'll take ownership of the day-to-day tactical management of ongoing studies ... This role reports to the Senior Director, Clinical Operations. Required Qualifications * Degree in ...
Clinical Project Managers
Salt Lake City, UT · On-site
$25K/mo
Utilize project management methodologies, coordinate with cross-functional teams, resolve issues ... Conduct work assignments as directed. Closely supervised with little latitude for independent ...
Clinical Project Managers
Salt Lake City, UT · On-site
$25K/mo
Utilize project management methodologies, coordinate with cross-functional teams, resolve issues ... Conduct work assignments as directed. Closely supervised with little latitude for independent ...
Clinical Project Manager
Los Angeles, CA · On-site
Mark Prince, Associate Professor and Director of My Mental Health Data Analysis and Dissemination, the Clinical Project Manager will play a central role in coordinating research operations, ensuring ...
Clinical Project Manager
Los Angeles, CA · On-site
Mark Prince, Associate Professor and Director of My Mental Health Data Analysis and Dissemination, the Clinical Project Manager will play a central role in coordinating research operations, ensuring ...
Clinical Project Manager
Franklin, TN · On-site
Project Management experience within a CRO is highly desirable. Primary Responsibilities Identifies project guidelines and communication needs by: * Reviewing study requirements and response ...
Clinical Project Manager
Franklin, TN · On-site
Project Management experience within a CRO is highly desirable. Primary Responsibilities Identifies project guidelines and communication needs by: * Reviewing study requirements and response ...
Clinical Project Manager
Princeton, NJ · On-site
Project Management experience within a CRO is highly desirable. Primary Responsibilities Identifies project guidelines and communication needs by: * Reviewing study requirements and response ...
Clinical Project Manager
Princeton, NJ · On-site
Project Management experience within a CRO is highly desirable. Primary Responsibilities Identifies project guidelines and communication needs by: * Reviewing study requirements and response ...
Manage inventory and accountability of clinical study supplies and investigational products ... Support Clinical Project Management and/or Site Management & Monitoring with other administrative ...
Manage inventory and accountability of clinical study supplies and investigational products ... Support Clinical Project Management and/or Site Management & Monitoring with other administrative ...
Clinical Project Manager
Waltham, MA · On-site
$129K - $194K/yr
Clinical Project Manager We are seeking a Clinical Project Manager to assist in leading the ... Excellent communication, presentation, and stakeholder management skills * Experience with late ...
Clinical Project Manager
Waltham, MA · On-site
$129K - $194K/yr
Clinical Project Manager We are seeking a Clinical Project Manager to assist in leading the ... Excellent communication, presentation, and stakeholder management skills * Experience with late ...
Bachelor's degree in life sciences or related field * 5-8+ years of experience of program management in biotechnology, pharmaceutical, or clinical research settings * Experience with project ...
Bachelor's degree in life sciences or related field * 5-8+ years of experience of program management in biotechnology, pharmaceutical, or clinical research settings * Experience with project ...
Clinical Project Manager
Waltham, MA · On-site
$130K - $150K/yr
... study management, overseeing the CRO and other vendors and helping to ensure the quality of ... In collaboration with the Director of Clinical Operations the CPM will lead functional team members ...
Clinical Project Manager
Waltham, MA · On-site
$130K - $150K/yr
... study management, overseeing the CRO and other vendors and helping to ensure the quality of ... In collaboration with the Director of Clinical Operations the CPM will lead functional team members ...
Clinical Project Manager
Lexington, MA · On-site
Candidate should be an Associate Director level, with 10+ yrs. of clinical operations experience with extensive project management experience. Ideal candidate will have experience in participating in ...
Clinical Project Manager
Lexington, MA · On-site
Candidate should be an Associate Director level, with 10+ yrs. of clinical operations experience with extensive project management experience. Ideal candidate will have experience in participating in ...
Director Clinical Project Management information
See salary details
$18K - $33K
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$100.1K is the 25th percentile. Wages below this are outliers.
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22% of jobs
The median wage is $121K / yr.
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15% of jobs
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$124.4K
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How much do director clinical project management jobs pay per year?
What does a Director of Clinical Project Management do?
What are the key skills and qualifications needed to thrive as a Director of Clinical Project Management, and why are they important?
What is the difference between Director Clinical Project Management vs Clinical Project Manager?
| Aspect | Director Clinical Project Management | Clinical Project Manager |
|---|---|---|
| Responsibilities | Oversees multiple projects, strategic planning, team leadership | Manages individual clinical trials, day-to-day operations |
| Experience & Credentials | Typically requires 8+ years, advanced degrees, leadership experience | Usually 3-5 years, relevant clinical or project management certifications |
| Work Environment | Senior management, cross-functional teams, strategic meetings | Project teams, site coordination, operational tasks |
The main difference is that the Director Clinical Project Management holds a senior leadership role overseeing multiple projects and strategic initiatives, while the Clinical Project Manager focuses on managing individual clinical trials and operational activities. Both roles require relevant experience and certifications, but the director's scope is broader and more strategic.
What are some common challenges faced by a Director of Clinical Project Management, and how can they be addressed?

Full-time
Posted 25 days ago
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
53rd of 207 rated it services
Job description
Customer dedicated Clinical Project Management Director taking an Indication Director role to provide operational delivery oversight for select indication(s). Provides strategic and operational leadership for indication-level delivery, translating strategy into effective execution from phase II to submission while ensuring clinical trials are delivered on time and to plan. The role aligns resource planning with program needs, supports cross-functional team leadership, and drives problem-solving, risk management, and decision-making across studies within the indication. Acting as a key liaison between IQVIA and customer, it ensures clear communication, accountability, and alignment to partnership goals, while fostering a high-performing, innovative team culture grounded in customers operating principles. Focus on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customers.
CompetenciesLeadership & Influence:Ability to lead cross-functional teams, inspire collaboration, and drive performance.
Strategic Thinking:Skilled in translating high-level strategy into actionable operational plans.
Problem-Solving:Solution-oriented mindset with strong risk identification and mitigation skills.
Communication:Excellent verbal and written communication skills for stakeholder engagement and decision-making.
Change Management:Demonstrated ability to implement organizational principles and foster continuous improvement.
Cultural Alignment:Role models humility, co-creation, and excellence while empowering teams and promoting innovation.
Understand project strategy and operationalize the agreed upon approach.
Oversee the development of integrated study management plans with the core project team.
Direct the execution of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
Recognize systemic issues at program or portfolio level and identify solutions with the project teams, recommend actions to improve efficiencies and oversee the implementation of best practices, address escalation items with the customer.;
Set objectives of the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
Monitor progress against contract and prepare/present project information proactively to all stakeholders internally and externally.
Responsible for the management and delivery of large and/or complex studies or programs of studies.
May be responsible for portfolio management with one customer or therapeutic area.
Proactively manage strategic risk (positive and negative) and contingencies and lead problem solving and resolution efforts.
Achieve project quality by identifying quality risks and issues, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.
Serve as primary project/program/portfolio contact with customer and own relationship with key customer contact(s), communicate/collaborate with IQVIA business development as necessary.;
Drive consistency of operational delivery across customer's projects/programs/portfolio.
Build the cross-functional project/program/portfolio team and lead their efforts, responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;
Responsible for ensuring the financial success of project/programs/portfolio.
Forecast and identify opportunities to accelerate activities to bring revenue forward.
Identify changes in scope and manage change control process as necessary, identify opportunities to increase scope to assist the Customer's business needs.;
Identify and communicate strategic lessons learned and best practices to promote continuous improvement.
Participate in, champion and adopt function and/or corporate initiatives, changes and/or special project assignments, act as a client liaison, departmental cross-functional liaison and/or change agent.;
Provide input to line managers of their project team members' performance relative to project tasks. Recommend team members' further professional development. Support staff development. Mentor less experienced project team members on assigned projects to support their professional development.
QualificationsIndustry experience in Biotech or BioPharma.
Proven track record in indication-level strategy and delivery withina CRO orpharmaceutical or biotech environment.
Bachelor's Degree Life sciences or related field
Minimum 12 years of industry, clinical research experience preferred, including significant operational leadership in global trials.
Requires extensive knowledge of multiple job areas obtained through advanced education and experience.
Viewed as a leading expert within the field by peers.
Strong understanding of clinical development processes, regulatory requirements, and GCP compliance.
Experience in resource forecasting and strategic planning for complex programs.
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. Learn more athttps://jobs.iqvia.com
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
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 $125,900.00 - $350,900.00. 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.About IQVIA
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At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US