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Irt Project Manager Jobs in New York (NOW HIRING)

Clinical Supply Chain Project Leader

Newark, NJ ยท On-site +1

$105K - $151K/yr

Project Management experience โ€‹ Preferred Qualifications: * Experience with GxP regulations and IMP requirements * Any experience with N-SIDE forecasting systems, IRT systems preferred * Risk ...

Clinical Supply Chain Project Leader

Manhattan, NY ยท On-site +1

$105K - $151K/yr

Project Management experience โ€‹ Preferred Qualifications: * Experience with GxP regulations and IMP requirements * Any experience with N-SIDE forecasting systems, IRT systems preferred * Risk ...

Clinical Supply Chain Project Leader

Paterson, NJ ยท On-site +1

$105K - $151K/yr

Project Management experience โ€‹ Preferred Qualifications: * Experience with GxP regulations and IMP requirements * Any experience with N-SIDE forecasting systems, IRT systems preferred * Risk ...

Clinical Supply Chain Project Leader

Elizabeth, NJ ยท On-site +1

$105K - $151K/yr

Project Management experience โ€‹ Preferred Qualifications: * Experience with GxP regulations and IMP requirements * Any experience with N-SIDE forecasting systems, IRT systems preferred * Risk ...

... or IRT functions. * Ability to demonstrate good project management skills. * Ability to create effective working relationships with internal and external stakeholders. * Ability to demonstrate ...

... IRT, ePRO). Utilizes project management tools to track study progress and plan work. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions

... IRT, ePRO). Utilizes project management tools to track study progress and plan work. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions

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Showing results 1-20

Irt Project Manager information

See New York salary details

$48.7K

$105.6K

$169K

How much do irt project manager jobs pay per year?

As of Aug 10, 2026, the average yearly pay for irt project manager in New York is $105,640.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,100.00 and $123,600.00 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?

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.
What are popular job titles related to Irt Project Manager jobs in New York? For Irt Project Manager jobs in New York, the most frequently searched job titles are:
What cities in New York are hiring for Irt Project Manager jobs? Cities in New York with the most Irt Project Manager job openings:
Infographic showing various Irt Project Manager job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $105,640 per year, or $50.8 per hour.

Senior Associate SP&L

Daiichi Sankyo, Inc.

Basking Ridge, NJ โ€ข On-site

$100K - $151K/yr

Full-time

Re-posted 22 days ago


Job description

Senior Associate SP&L
Job Requisition ID: 653
Posting Start Date: 6/18/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
This is an operational position, task oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence to Project objectives, budget control and departmental collaborations. Work is escalated if outside of scope of role, and/or complexity? This position has strong knowledge of GMPs and GCPs and is compliant with domestic and foreign regulatory requirement but may seek support on such items from time to time. Has sufficient knowledge to Identify critical issues or problems with Projects and/or identification of issues which may compromise patient dosing or safety. Basic understanding of professional working environment as well as Quality Assurance and global regulatory requirements such that identification of risks is recognized and the need for CAPAs or reports on deviations is clearly understood. Basic knowledge of Import/export requirements to the extent that there is overall recognition of global differences exist and understanding of the need to address such issues or concerns. Experience with IRT systems and support in managing the forecasting and planning of drug supply needs Able to participate effectively on a cross functional and on Global teams.
Job Description
Responsibilities
Works, under supervision, with outsourcing to submit appropriate requirements on a project basis. Supports team in generating RFPs and in reviewing proposals and selecting vendors. This position also supports the management of the WO development and implementation. Supports packaging design and patient kit supply preparation, label generations and approvals and associated interactions with vendors. Supports regular vendor/sponsor discussions to identify risks and ongoing study support. Identifies critical issues which may compromise patient dosing or safety. Supports comparator sourcing requirements, RFP generation and working with outsourcing to submit appropriate requirements on a Project basis. Vendor Management - support interactions with Vendors on packaging design and patient kit supply preparation, label generations and approvals. Support regular vendor/sponsor discussions to identify risks and ongoing study support. Ensures on time site shipments for subject and patient dosing, and ensures that material is fully released prior to shipment to site Ensures compliance with all domestic and foreign regulatory requirements but may seek line management support when necessary. Basic knowledge of Import/export requirements to the extent that there is overall recognition of potential global issues as regards import license requirements, shipment delays and is able to communicate the issues and support resolution development. Support IRT design for control of drug dispensing and inventory management. Understand User specifications in support of IRT processes and basic concepts of IRT
Responsibilities Continued
Qualifications
Education Qualifications
Bachelor's Degree in Pharmacy or related field preferred PharmD preferred Master's Degree preferred
Experience Qualifications
4 or More Years related experience preferred
Experience in Project Management, Clinical Supply Management, and/or Clinical Trials Coordination required
Demonstrated experience in working on inventory management, forecasting, and distribution of drug supply needs, IXRS experience, managing vendors and contributing to budget control preferred
Additional Information
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$100,960.00 - USD$151,440.00
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