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$17K

$72.3K

$126K

How much do rtsm jobs pay per year?

As of Aug 22, 2026, the average yearly pay for rtsm in the United States is $72,301.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,500.00 and $98,000.00 per year, depending on experience, location, and employer.

What is an RTSM?

An RTSM (Randomization and Trial Supply Management) job involves managing clinical trial systems that handle patient randomization, drug assignment, and supply logistics. Professionals in this role ensure that trial participants receive the correct treatments while maintaining compliance with study protocols and regulations. They work closely with clinical operations, data management, and IT teams to configure and support RTSM software. Strong analytical skills and knowledge of clinical trial processes are essential for success in this role.

What does an RTSM do?

A typical day for an RTSM Specialist involves overseeing clinical trial randomization processes, managing drug inventory, and addressing queries from clinical study teams to ensure the smooth operation of trial supply systems. You may participate in cross-functional meetings, troubleshoot IRT platform issues, and generate essential reports for project stakeholders. Collaboration with clinical operations, data management, and regulatory teams is common, as accuracy and timeliness in participant randomization and supply logistics are critical. This role often requires balancing multiple studies and adapting to shifting project timelines, making organizational and communication skills crucial for success.

What are the key skills and qualifications needed to thrive as an RTSM?

To thrive as an RTSM (Randomization and Trial Supply Management) Specialist, you need expertise in clinical trial operations, data management, and a relevant bachelor's degree in life sciences or information technology. Familiarity with RTSM platforms (such as Medidata or Almac) and industry-standard certifications like GCP or IRT system training are highly beneficial. Strong attention to detail, problem-solving skills, and effective cross-functional communication are key soft skills in this position. These competencies are vital to ensure the accurate management of clinical trial supplies and randomization processes, maintaining regulatory compliance and supporting successful study outcomes.

More about Rtsm jobs

What states have the most Rtsm jobs?

States with the most job openings for Rtsm jobs include:

What job categories do people searching Rtsm jobs look for?

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Rtsm jobs near you
Infographic showing various Rtsm job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 5% Part Time, and 7% Contract. Highlights an 78% Physical, 2% Hybrid, and 20% Remote job distribution, with an average salary of $72,301 per year, or $34.8 per hour.

IRT/RTSM Script Writer

Dark Horse Consulting Group

Boston, MA • On-site

Part-time

This job post has expired today. Applications are no longer accepted.

Job description

We are seeking an experienced IRT/RTSM Script Writer to support our clients in the life sciences industry with IRT/RTSM design and implementation. This role will focus on IRT (Interactive Response Technology) design support, test script writing, and testing support for clinical trials. The ideal candidate will bring experience working closely with cross-functional clinical study teams, IRT/RTSM vendors, and external partners to ensure test scripts align with IRT design and clinical trial objectives. This is a part-time role.

Key Responsibilities
IRT/RTSM Design and Implementation Support
• Oversee IRT/RTSM design and implementation from user requirement specifications through Go-Live, ensuring alignment with clinical study protocol and functional requirements.
• Participate in client meetings, design sessions, and sandbox testing with the ability to suggest solutions for client problems.
• Develop and manage project plans to ensure timely completion of scripts, incorporating key milestones and activity timelines.
• Communicate IRT/RTSM implementation project status, accomplishments, risks, and issues to stakeholders.
• Identify, escalate, and drive resolution of project-related risks and challenges.
• Support Computer System Validation (CSV) activities for IRT/RTSM.
• Leverage templates and AI to develop scripts for IRT/RTSM User Acceptance Testing (UAT) and EDC integration.
• Provide live UAT testing support.

Qualifications & Experience
• Proven experience writing IRT test scripts for User Acceptance Testing.
• Knowledge of IRT/RTSM solutions, clinical trial design of Phase I-IV clinical trials, & clinical distribution strategies.
• Experience collaborating with IRT/RTSM vendors and cross-functional client teams to ensure seamless study execution.
• Ability to work in a fast-paced environment with the possibility of last-minute schedule changes.
• Available to work flexible hours though primarily standard East Coast business hours.
• Bachelor’s degree and 3 years of script writing experience required.