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Director Clinical Project Management Jobs in Indiana

... directing of major projects with broad requirements in Multidomain Operations focusing on ... and managing budgets and schedules. Requirements: Education: Bachelor's degree or equivalent ...

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Director Clinical Project Management information

See Indiana salary details

$17.1K

$118.4K

$174.1K

How much do director clinical project management jobs pay per year?

As of Sep 7, 2026, the average yearly pay for director clinical project management in Indiana is $118,355.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,100.00 and $140,400.00 per year, depending on experience, location, and employer.

What does a director of clinical project management do?

A Director of Clinical Project Management oversees the planning, execution, and completion of clinical trials within a pharmaceutical or biotech company. They lead project management teams, ensure regulatory compliance, manage budgets and timelines, and coordinate communication among stakeholders. Their responsibilities also include risk management, resource allocation, and ensuring trials meet both scientific and business objectives. This role is critical for bringing new medical treatments through the development pipeline to market approval.

What are some common challenges faced by a director of clinical project management, and how can they be addressed?

Directors of Clinical Project Management often encounter challenges such as managing complex, multi-site trials, maintaining regulatory compliance, and coordinating cross-functional teams. Balancing timelines, budgets, and quality expectations can also be demanding, especially when unexpected issues arise. Successful directors address these challenges by fostering clear communication, utilizing robust project management tools, and building strong relationships with stakeholders. Staying current with regulatory changes and providing mentorship to team members also helps ensure project success and professional growth.

What are the key skills and qualifications needed to thrive as a director of clinical project management, and why are they important?

To thrive as a Director of Clinical Project Management, you need deep expertise in clinical research, regulatory compliance, project leadership, and typically an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as PMP or CCRP are commonly required. Strong strategic thinking, communication, and team leadership skills help drive project success and foster collaboration among cross-functional teams. These competencies are vital for delivering clinical trials on time, within budget, and in compliance with regulatory standards.

What is the difference between Director Clinical Project Management vs Clinical Project Manager?

AspectDirector Clinical Project ManagementClinical Project Manager
ResponsibilitiesOversees multiple projects, strategic planning, team leadershipManages individual clinical trials, day-to-day operations
Experience & CredentialsTypically requires 8+ years, advanced degrees, leadership experienceUsually 3-5 years, relevant clinical or project management certifications
Work EnvironmentSenior management, cross-functional teams, strategic meetingsProject 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.

How much do director clinical project managements earn?

The salary for a Director of Clinical Project Management typically ranges from $120,000 to $180,000 annually, depending on experience, location, and the size of the organization. Senior roles with extensive experience and certifications like PMP or PMI-ACP can earn higher compensation, often including bonuses and benefits.

What are popular job titles related to Director Clinical Project Management jobs in Indiana?

For Director Clinical Project Management jobs in Indiana, the most frequently searched job titles are:

What cities in Indiana are hiring for Director Clinical Project Management jobs?

Cities in Indiana with the most Director Clinical Project Management job openings:

Associate Director Capital Project Management

AstraZeneca

Mount Vernon, IN • On-site

Full-time

Posted 11 days ago


AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical


Job description

The AstraZeneca Mt. Vernon site was established in 1972 and is the flagship site delivering innovative, life changing oral solid medicines. At the site we formulate and pack OSD tablets and capsules for over 60+ markets. The Mt Vernon site is complex, the largest AZ production site in the US with over 700+ employees. We are located in the southwest corner of the state of Indiana, approximately 15 miles from Evansville, Indiana - the third largest city in the state. The Mt. Vernon site is both collaborative and Inclusive. We have several employee resource groups (ERGs) onsite that are aimed at promoting, celebrating, and educating employees about diversity, inclusion, philanthropy, networking, etc. Each of these groups provide employees with opportunities for interactive and engaging events and initiatives which enhance professional development and provide opportunities to engage with likeminded co-workers.
It is important to us that each employee feels welcome to bring their whole self to work every day. Here is a sneak peek of some of "perks" the MTV site offers: on-site fitness center with access to a personal trainer, on-site walking trail, walking desk, on-site basketball court, ping pong, massage chair, lunch & learns, sustainable & ergonomic office working environment, tuition reimbursement, training/ lifelong learning opportunities, book club, dining center with hot meals, snack market, free coffee and hot tea, climate controlled work environment.
Join us as an Associate Director Capital Project Management, where you will be responsible for the planning, design, and implementation of capital projects. This role is not just about managing projects, but also about strategic collaboration with cross-functional site and global teams to support business operation strategies and improvement opportunities. You will be communicating with global partners to ensure design standards, equipment, Factory of the Future and compliance initiatives are aligned.
Accountabilities:
As an Associate Director Capital Project Management, you will lead, direct and manage cross-functional site and global project teams. You will comprehend strategic project requirements and translate those into detailed capital project plans aligned with business initiatives. You will establish strong working relationships with key internal and external customers and demonstrate personal ownership and accountability for results with a focus on customer service. You will proactively identify potential issues and opportunities, develop contingency plans as required, and guide conflict resolution at the project team level.
Essential Skills/Experience:
- Bachelor's degree required, preferably in Engineering or other related technical discipline.
- Minimum 8+ years of relevant experience
- Experience in conceptual development, project management (planning and scheduling projects), design, and implementation of major capital projects.
- Hands-on experience in the negotiation and management of contracts and agreements with engineering contractors, vendors, regulatory, and government agencies.
- Knowledge and understanding of validation and qualification principles, project management, and change control principles.
- Ability to understand and apply financial analyses to make good decisions in a manufacturing environment.
- Excellent verbal, written, and interpersonal communication skills are essential.
- Experience in developing and introducing an initiative and gaining subsequent on board and support from different levels within the organization.
- Direct knowledge in Engineering Standards.
Desirable Skills/Experience:
- Master's degree is highly desirable.
- People leadership
- Experience in the pharmaceutical industry and related regulatory, engineering, and construction techniques.
- Professional certifications.
- Experience working with regulatory agencies such as OSHA, EPA, FDA, and DEA
At AstraZeneca, we are leading our Operations function at an exciting time of growth and evolution. We pioneer new approaches and processes across our sites, empowering our teams to cultivate a Lean mentality and sustainable practices. Every change we make is to deliver better outcomes for our patients. We are inspiring and credible leaders, ensuring everyone on our site has a platform and opportunity to speak up and share their ideas. We respect our teams and bring them on a journey. Working with our knowledgeable employees, we understand the importance of getting their on board to our decisions.
Are you ready to be part of a team that fosters trust to get the best out of others? Join us today!
Date Posted
27-Aug-2026
Closing Date
14-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB