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Irt Project Manager Jobs (NOW HIRING)

Exelixis

Clinical Supplies Manager II

Alameda, CA · On-site

$132K - $188K/yr

Monitor and manage clinical supply activities through IRT from study start-up through study closure ... Utilize appropriate software and IT systems to effectively manage key project activities.

Icon plc

RTSM/eCOA Manager

Blue Bell, PA · On-site

Handson experience working with RTSM/IRT/eCOA vendors; vendor management experience required. * Project management experience managing complex, matrixed studies or programs. * Familiarity with ...

Exelixis

Clinical Supplies Manager II

Alameda, CA

$132K - $188K/yr

Monitor and manage clinical supply activities through IRT from study start-up through study closure ... Utilize appropriate software and IT systems to effectively manage key project activities.

Simbec-Orion

Project Director

Boston, MA

Manage and identify vendors who provide services in support of the projects (for example, IRT/RTSM, third party laboratories, meeting organisers). * Management and reporting of project finances ...

Almac Group

Clinical Supply Manager

Durham, NC · On-site

IRT * Client-facing position or customer service related * Project Management Qualification (i.e., PMP, Prince 2) * GMP and/or GCP knowledge * Working knowledge of the drug development process * MS ...

Suvoda

Software Developer

They are seeking a Software Developer II to work within a cross-functional project team to develop Interactive Response Technology (IRT) for randomization and drug supply management, ensuring the ...

Suvoda

Software Developer

They are seeking a Software Developer II to work within a cross-functional project team to develop Interactive Response Technology (IRT) for randomization and drug supply management, ensuring the ...

Ardelyx

Clinical Trial Manager

Newark, CA · On-site +1

$136K - $160K/yr

Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT ... Strong project management skills, including managing of timelines, budgets, and cross-functional ...

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All JobsIrt Project Manager Jobs

Irt Project Manager information

See salary details

$44.5K

$96.6K

$154.5K

How much do irt project manager jobs pay per year?

As of Jun 27, 2026, the average yearly pay for irt project manager in the United States is $96,560.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $113,000.00 per year, depending on experience, location, and employer.

What is the difference between Irt Project Manager vs Irt Coordinator?

AspectIrt Project ManagerIrt Coordinator
CredentialsTypically requires a bachelor's degree in a related field and project management certificationsUsually requires a high school diploma or associate degree, with some industry-specific training
Work EnvironmentLeads projects, manages teams, and oversees budgets in technical or industrial settingsSupports project activities, coordinates schedules, and assists with documentation
Employer & Industry UsageCommon in construction, engineering, and manufacturing industriesOften found in similar industries, supporting project teams and operations
Search & Comparison IntentPeople compare roles to understand project leadership responsibilitiesIndividuals look to distinguish support roles from management positions

The Irt Project Manager typically holds more responsibilities, including leading projects and managing teams, while the Irt Coordinator focuses on supporting project activities and coordination. Both roles are essential in technical industries, but the Project Manager has a broader scope of authority and decision-making.

What is an IRT Project Manager?

An IRT Project Manager oversees the implementation and management of Interactive Response Technology (IRT) systems in clinical trials. These systems are used to manage patient randomization, drug supply, and data collection efficiently. The IRT Project Manager acts as a liaison between sponsors, clinical teams, and technology providers to ensure that the IRT system meets all study requirements and timelines. Their responsibilities include project planning, system customization, user training, and troubleshooting throughout the study lifecycle.

How does an IRT Project Manager typically collaborate with clinical trial teams during a project's lifecycle?

An IRT (Interactive Response Technology) Project Manager works closely with clinical trial teams, including clinical operations, data management, and vendors, to ensure that IRT systems are developed, tested, and deployed according to study requirements. They facilitate regular meetings to gather requirements, provide system updates, and address any issues that arise during the trial. Effective collaboration is key, as the IRT Project Manager acts as the bridge between technical teams and clinical stakeholders, ensuring smooth communication and timely delivery of system functionalities essential for trial success.

What are the key skills and qualifications needed to thrive as an IRT Project Manager, and why are they important?

To thrive as an IRT Project Manager, you need expertise in clinical trial management, strong organizational skills, and a background in life sciences or a related field. Familiarity with Interactive Response Technology (IRT) systems, project management tools like MS Project, and regulatory requirements is typically required, along with certifications such as PMP being advantageous. Excellent communication, problem-solving abilities, and attention to detail help you effectively coordinate between sponsors, vendors, and cross-functional teams. These skills ensure successful implementation and maintenance of IRT systems, supporting clinical trial integrity and compliance.
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What cities are hiring for Irt Project Manager jobs? Cities with the most Irt Project Manager job openings:
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Irt Project Manager jobs near you
Infographic showing various Irt Project Manager job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $96,560 per year, or $46.4 per hour.
Clinical Supplies Manager II

Clinical Supplies Manager II

Exelixis

Alameda, CA • On-site

$132K - $188K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Job description

SUMMARY/JOB PURPOSE:
The Clinical Supplies Manager II oversees all aspects of clinical supply management including packaging, labeling, monitor inventory levels, and distribution by interacting with internal and external supply partners/vendors to ensure supply of IMP are sufficient at depots and clinical sites.
Essential Duties And Responsibilities:
  • Lead effort for clinical supply management functionality.
  • Monitor and manage clinical supply activities through IRT from study start-up through study closure.
  • Proactively drive the labeling, packaging, release, distribution of clinical supplies at external CMO's for assigned studies, ensuring the project timeline is met or exceeded.
  • Ensure domestic and global distribution arrangements are in place with external vendors to allow shipment following availability of technical and regulatory releases.
  • In collaboration with relevant partners, create forecasts and packaging design based on study needs to ensure optimized supply plan.
  • Partner with key stakeholders (including Quality Assurance and Regulatory Affairs) to ensure supplies are labelled and released for clinical site shipment for global clinical trials.
  • Work cross-functionally to develop IRT to develop specifications and perform UAT.
  • Design and/or review label text to meet product requirements and ensure compliance with US and international regulations.
  • Represent clinical supplies function at clinical trial team meetings; communicate plan and timelines to internal and external customers and partners.
  • Work with cross-functional teams to develop specifications and user testing of IRT systems provided by 3rd party vendors.
  • Ensure appropriate system documentation is transferred to TMF and ready for inspection readiness.
  • Utilize appropriate software and IT systems to effectively manage key project activities.

Supervisory Responsibilities:
  • None

EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:
Education/Experience:
  • BS/BA degree in related discipline and a minimum of seven years of related experience; or,
  • MS/MA degree in related discipline and a minimum of five years of related experience; or,
  • Equivalent combination of education and experience.
  • Certification in assigned areas is a plus.

Experience/The Ideal for Successful Entry into Job:
  • Demonstrated experience with clinical supply management planning, labeling, packaging, and distribution.
  • Clinical Supply management experience using contract manufacturing companies strongly preferred.
  • Working knowledge and experience with Interactive Response Technologies (IRT) such as IVRS and IWRS

Knowledge/Skills:
  • Willingness to work in a fast paced, evolving environment.
  • Knowledge of GMP batch record development, review, and approval processes.
  • Knowledge of Interactive Voice/Web response systems for use in clinical studies.
  • Working knowledge of regulations relating to clinical labeling, packaging and distribution activities.
  • Working knowledge of GMP/GCP/GLP regulations required.
  • Excellent project management and communication skills.

JOB COMPLEXITY:
  • Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
  • Uses professional concepts and company objectives to resolve moderate to complex issues in creative and effective ways.
  • May also work on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors.
  • Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results.
  • Networks with key contacts outside own area of expertise.

Working Conditions:
  • 20% travel to vendor sites, team meetings, and/or other offices.

Work Environment/Physical Demands:
Our office is a modern, open-plan space that foster collaborations and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.
#LI-MB1
If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!
Our compensation reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $132,500 - $188,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.
In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.
DISCLAIMER
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

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