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Senior Clinical Project Manager Jobs in Indiana (NOW HIRING)

The Clinical Project Manager within the Program Management Organization (PMO) is expected to provide project management support to internal team members, as well as customers, to deliver Azenta Life ...

The Clinical Project Manager within the Program Management Organization (PMO) is expected to provide project management support to internal team members, as well as customers, to deliver Azenta Life ...

Description The Senior Project Manager provides leadership and oversight for a growing portfolio of custom software applications that support clinical education, academic affairs, continuing ...

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Senior Project Manager

Indianapolis, IN · On-site

$100K - $145K/yr

Project Manager / Senior Project Manager Department: Engineering - Water Utility Infrastructure Location: Indianapolis, IN Employment Type: Full-Time Compensation: $100K - $145K (commensurate with ...

Senior Project Manager

Indianapolis, IN · On-site

$100K - $145K/yr

Project Manager / Senior Project Manager Department: Engineering - Water Utility Infrastructure Location: Indianapolis, IN Employment Type: Full-Time Compensation: $100K - $145K (commensurate with ...

Senior Project Manager

Indianapolis, IN · On-site

$75K - $125K/yr

Senior Project Manager Company: The Ghoman Group Position: Senior Project Manager Employment Type: Full-Time, Permanent Location: 5855 Rockville Rd, Indianapolis, IN 46224 Salary: $75,000 - $125,000 ...

Senior Project Manager

Indianapolis, IN · On-site

$75K - $125K/yr

Senior Project Manager Company: The Ghoman Group Position: Senior Project Manager Employment Type: Full-Time, Permanent Location: 5855 Rockville Rd, Indianapolis, IN 46224 Salary: $75,000 - $125,000 ...

Senior Project Manager Company: The Ghoman Group Position: Senior Project Manager Employment Type: Full-Time, Permanent Location: 5855 Rockville Rd, Indianapolis, IN 46224 Salary: $75,000 - $125,000 ...

Senior Project Manager

Sullivan, IN · On-site

$200K - $215K/yr

Senior Project Manager Location: Sullivan, IN Division: Enerfab Power & Industrial - Evansville Direct Report: Project Executive Salary Range: $200,000 - $215,000 Company Summary: Enerfab has over ...

Senior Project Manager

Sullivan, IN · On-site

$200K - $215K/yr

Senior Project Manager Location: Sullivan, IN Division: Enerfab Power & Industrial - Evansville Direct Report: Project Executive Salary Range: $200,000 - $215,000 Company Summary: Enerfab has over ...

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Showing results 1-20

Senior Clinical Project Manager information

See Indiana salary details

$49.5K

$110K

$191.3K

How much do senior clinical project manager jobs pay per year?

As of Aug 24, 2026, the average yearly pay for senior clinical project manager in Indiana is $109,981.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,100.00 and $136,100.00 per year, depending on experience, location, and employer.

What is a senior clinical project manager?

A Senior Clinical Project Manager is a professional responsible for overseeing and managing clinical trials and research projects within the pharmaceutical, biotechnology, or medical device industries. They coordinate all aspects of a clinical study, including planning, execution, budgeting, and compliance with regulatory requirements. Senior Clinical Project Managers lead cross-functional teams, communicate with stakeholders, and ensure that clinical trials are completed on time, within scope, and according to quality standards. Their expertise is crucial for the successful development of new treatments and therapies.

What does a senior clinical project manager do?

As a senior clinical project manager, your responsibilities center around the management of a clinical trial team. You assign projects, ensure the success of team activities, and enforce company regulations. Your duties include staying within the scope of a budget while carrying out a clinical trial. You manage your team through each study as you plan out their responsibilities, keeping the project on track and cost-effective. As a senior clinical project manager, you create reports on the efficiency and progress of each clinical trial.

What are the key skills and qualifications needed to thrive as a senior clinical project manager?

To thrive as a Senior Clinical Project Manager, you need in-depth knowledge of clinical research, regulatory requirements, project management methodologies, and typically a 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 equivalent are commonly required. Strong leadership, problem-solving, and communication skills help manage cross-functional teams and stakeholder expectations. These skills and qualifications ensure efficient trial execution, regulatory compliance, and the successful delivery of clinical projects within timelines and budgets.

How does a senior clinical project manager typically collaborate with cross-functional teams throughout a clinical trial?

A Senior Clinical Project Manager plays a pivotal role in coordinating cross-functional teams, such as clinical operations, data management, biostatistics, regulatory affairs, and vendors. They facilitate regular meetings, ensure effective communication, and resolve any interdepartmental issues that may arise during the study. By fostering collaboration and aligning team objectives, they help maintain timelines, manage resources, and ensure the trial progresses smoothly and compliantly. This collaborative approach is essential for the successful execution and delivery of clinical projects.

What is the difference between Senior Clinical Project Manager vs Clinical Project Manager?

AspectSenior Clinical Project ManagerClinical Project Manager
Required CredentialsTypically requires 5+ years of experience, advanced certifications (e.g., PMP), and strong leadership skillsUsually requires 2-4 years of experience, relevant certifications, and foundational project management skills
Work EnvironmentLeads multiple projects, manages teams, and interacts with senior stakeholdersManages individual projects, coordinates with teams, and reports to senior managers
Employer & Industry UsageCommonly employed in pharmaceutical, biotech, and CRO companies for complex projectsUsed across similar industries for managing clinical trials at various scales

The main difference between a Senior Clinical Project Manager and a Clinical Project Manager lies in experience, leadership responsibilities, and project scope. Senior roles involve overseeing multiple projects and guiding teams, while Clinical Project Managers focus on managing specific clinical trials. Both roles require relevant certifications and industry experience, but the senior position demands more strategic oversight and leadership skills.

What are popular job titles related to Senior Clinical Project Manager jobs in IN?

For Senior Clinical Project Manager jobs in IN, the most frequently searched job titles are:

Infographic showing various Senior Clinical Project Manager job openings in Indiana as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $109,981 per year, or $52.9 per hour.

Clinical Project Manager II

Azenta

Plainfield, IN • On-site

Full-time

Posted 7 days ago


Azenta Life Sciences rating

7.5

Company rating: 7.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

64th of 120 rated laboratories


Job description

Azenta Inc.
At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.
All we accomplish is grounded in our core values of Customer Focus, Achievement, Accountability, Teamwork, Employee Value and Integrity

Job Title
Clinical Project Manager II
Job Description
At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer-focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.
Azenta Life Sciences is a global leader in the life sciences space with headquarters with offices and operations worldwide. We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally. We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the largest installed base managing over 1 billion samples globally.
How You'll Add Value:
The Clinical Project Manager within the Program Management Organization (PMO) is expected to provide project management support to internal team members, as well as customers, to deliver Azenta Life Sciences solutions (Long Term Sample Management, Active Clinical Trial Sample Management, Regulated Products (GMP/GTP) Management) to clients, partners, and alliances. Under guidance from the Director, Clinical Program Management or Program Manager, the Clinical Project Manager is expected to gain an in-depth understanding of the key clients and become an expert in Azenta Life Sciences services.
What You'll Do:
  • Serve as the primary client contact for assigned projects and establish working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business
  • Ensure that all customer expectations are documented and acted upon in compliance with regulatory requirements
  • Able to act efficiently in an environment with dynamic timelines and priorities
  • Accountable for the monitoring and reporting of performance metrics
  • Create required project plans
  • Implement and monitor progress against project plans and revise as necessary
  • Monitor project schedule and scope to ensure both remain on track
  • Project support may include kit provision and logistics, sample management, lab services support, relocation services, training, management, or support of alliances/ partnerships
  • Proactively engage in both quality assurance and risk management activities to ensure project deliverables are met according to both Azenta Life Sciences and client requirements
  • Participate in pre-sale discussions and client meetings as required
  • Actively participate in Azenta Life Sciences development through continuous improvement initiatives, contributing to Azenta's culture of quality and productivity initiatives including the development of new processes and SOPs, and the maintenance of SOPs to maintain audit-ready alignment with the Azenta Business Systems
  • Mentor Client Coordinator as needed
  • Managing queries and resolutions

What You Will Bring:
  • Bachelor's degree in science or related field with a minimum of 2 years of project management experience
  • OR High School Diploma or its equivalent and a minimum experience of 5 years of project management experience
  • Experience working in an FDA and GXP regulated environments.
  • Preferred master's degree in science or related field
  • Preferred CSPO, CSM, PMP
  • Strong organizational skills and attention to detail
  • Excellent verbal and written communication skills; presentation skills, ability to engage in effective problem-solving conversations
  • Demonstrated ability to collaborate and gain commitment from others
  • Demonstrated ability to prioritize work, customers, internal and external demands
  • Demonstrated ability to complete long-range projects as assigned

Your Working Conditions:
  • General office setting
  • The Employee may occasionally travel, up to 10% of working time
  • The Employee may occasionally work in an area with potentially infectious materials
  • The Employee will be responsible for maintaining a clean work environment and enforcing and following Universal Precautions for bloodborne pathogens when working in an area considered to be potentially contaminated

Join us and help enable life-changing discoveries by keeping critical life science systems running reliably-every day.
#IND123
If any applicant is unable to complete an application or respond to a job opening because of a disability, please email at Recruiting@azenta.com for assistance.
Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race, color, age, religion, gender, sexual orientation, gender identity, national origin, disability or veteran status.
United States Base Compensation: $74,000.00 - $93,000.00
The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience, education (including licensure and certifications), qualifications, performance, and geographic location, among other relevant business or organizational needs.

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