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Project Manager, IRT

Blue Bell, PA · Remote

We have an incredible opportunity for a Project Manager to join ICON's Interactive Response Technology (IRT) team. The IRT PM will be responsible for overseeing the implementation and management of ...

ICON

Project Manager, IRT

Blue Bell, PA · On-site

We have an incredible opportunity for a Project Manager to join ICON's Interactive Response Technology (IRT) team. The IRT PM will be responsible for overseeing the implementation and management of ...

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Irt Interactive Response Technologies information

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How much do irt interactive response technologies jobs pay per year?

As of Sep 12, 2026, the average yearly pay for irt interactive response technologies in the United States is $88,001.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,000.00 and $90,000.00 per year, depending on experience, location, and employer.

What is an IRT Interactive Response Technologies?

An IRT (Interactive Response Technologies) job typically involves managing and supporting systems used in clinical trials for randomization, drug supply management, and patient tracking. Professionals in this field work with stakeholders to design, implement, and maintain IRT solutions that ensure trial efficiency and compliance. They often collaborate with sponsors, CROs, and technology vendors to configure systems, troubleshoot issues, and optimize workflows. Strong technical, analytical, and communication skills are essential for success in this role.

What are the key skills and qualifications needed to thrive in the IRT Interactive Response Technologies position?

To excel in Interactive Response Technologies (IRT), candidates typically need a strong background in information technology, project management, and clinical trial processes, often supported by degrees in computer science or life sciences. Familiarity with IRT platforms, software validation, GCP (Good Clinical Practice), and data management tools is highly valued, along with certifications such as PMP or specific IRT system training. Strong analytical thinking, attention to detail, and effective communication skills help professionals perform well in cross-functional teams. These competencies are essential to ensure the reliability, compliance, and seamless implementation of IRT systems in clinical research environments.

What are some of the typical challenges faced in an IRT Interactive Response Technologies role and how do professionals address them?

Professionals in IRT roles frequently encounter challenges such as managing complex study requirements, adapting to evolving clinical trial protocols, and ensuring data integrity amidst tight timelines. Addressing these challenges often involves close collaboration with project teams, continuous training on new technologies, and meticulous attention to regulatory compliance. Successful IRT specialists proactively communicate with stakeholders to resolve technical issues quickly, and they stay updated with industry best practices to maintain system efficiency. These efforts are essential for supporting the success of clinical trials and ensuring that IRT solutions are robust, reliable, and user-friendly.

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Irt Interactive Response Technologies jobs near you
Infographic showing various Irt Interactive Response Technologies job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 91% Full Time, 5% Part Time, 2% Contract, and 1% Nights. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $88,001 per year, or $42.3 per hour.

Clinical Supply Chain Project Manager

Inglewood, CA • On-site

American Shengsheng Supply Chain
See more jobs at American Shengsheng Supply Chainexternal

Full-time

Re-posted 20 days ago

Job description

Description:

We are seeking a Clinical Supply Chain Project Manager to oversee clinical trial supply planning and execution across multiple projects. The successful candidate will be responsible for coordinating the sourcing, packaging, labeling, distribution, and inventory management of investigational medicinal products (IMPs) and related supplies throughout the clinical trial lifecycle. This role requires strong cross-functional collaboration, project management skills, and regulatory knowledge to ensure reliable drug supply to clinical sites.
  

Key Responsibilities:
  • Assist in developing appropriate drug supply plans across all phases of a clinical trial, including forecasting and managing investigational product demand.
  • Identify, evaluate, and manage suppliers for trial materials (including drugs, consumables, and auxiliary equipment), as well as labeling and packaging print vendors.
  • Lead the design and/or review of label text and packaging mock-ups.
  • Communicate drug supply plans and timelines to internal functional teams, sponsors, and CROs; coordinate depot activities including receipt, repackaging, labeling, inventory management, distribution, temperature control, returns, and destruction.
  • Monitor drug stock levels at depots and clinical sites to ensure uninterrupted drug supply throughout the study.
  • Provide input on IRT (Interactive Response Technology) specifications to optimize drug utilization and prevent supply shortages at sites.
  • Collaborate with IRT vendors to design and manage reporting systems for drug usage, forecasting, and depot-level inventory tracking across the project lifecycle.
Requirements:

Qualifications:

  • Bachelor’s degree or above; background in Pharmacy preferred.
  • Minimum 3 years of experience in clinical project management or pharmaceutical supply chain; prior team management experience is a plus.
  • Familiar with ICH-GCP, China GCP, GMP, GSP, and WHO GDP regulations.
  • Strong communication, problem-solving, and interpersonal skills.
  • Detail-oriented, reliable, and able to work under pressure.
  • Experience with cross-timezone collaboration