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4G Clinical

Software Integrations Lead

Wellesley, MA · On-site +1

Maintain knowledge of Prancer RTSM/Admin and serve as the SME ensuring integration design is compatible with Prancer study design * Logs, tracks and drives resolution of functional and technical ...

Procom Consultants Group

BMS Consultant

Plano, TX · On-site

BMS Consultant Mandatory Skills Hands-on experience and deep expertise in deployment of IT Service Management solution including HP BSM, BSM RTSM, HP uCMDB, SCOM Experience in HP's Business Service ...

Metasys

HP UD/UCMDB Consultants

Alexandria, VA · On-site

... RTSM and push to APM/OMi Configure up to five (5) Asset Inventory Reports Create one (1) custom configuration management policy Integrations o Integrate UCMDB with RTSM database for BSM/OMi o ...

SystImmune, Inc

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Build and configure Medidata Rave RTSM modules, including randomization schemes, stratification factors, depot/kit management, and resupply algorithms. * Manage integrations with third-party RTSM/IRT ...

Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Build and configure Medidata Rave RTSM modules, including randomization schemes, stratification factors, depot/kit management, and resupply algorithms. * Manage integrations with third-party RTSM/IRT ...

Cube Hub Inc.

Supply Chain IRT Specialist

Gaithersburg, MD · On-site

$46 - $50/hr

Hands-on experience with specialized IRT/RTSM/IxRS software architectures developed by industry vendors (e.g., Suvoda, Perceptive, Signant Health, 4G Clinical, Endpoint, etc.). * Prior experience ...

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How much do rtsm jobs pay per year?

As of Jul 15, 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 job?

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 are the key skills and qualifications needed to thrive in the Rtsm position, and why are they important?

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.

What does a typical day look like for an RTSM Specialist in a clinical research organization?

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.

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Rtsm jobs near you
Senior Manager, RTSM Lead, Clinical Supply & External Manufacturing

Senior Manager, RTSM Lead, Clinical Supply & External Manufacturing

Alexion Pharmaceuticals

Boston, MA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Introduction to role:
Are you ready to lead the systems that keep clinical trials supplied, blinded, and on time? As Senior Manager, RTSM Lead, you will shape how we design and run IRT/RTSM across global studies, translating standards into practice and vendor partnerships into reliable delivery. Based in Boston, you will sit at the heart of our clinical supply ecosystem, making sure every site gets the right medicine for the right patient at the right moment.
Your work will safeguard data integrity and patient safety while shortening study timelines for people living with rare and devastating conditions. You will guide cross-functional teams, elevate quality through robust UAT and governance, and bring best-in-class solutions into our operating model. How will you use your expertise to unlock smarter, faster trials that reach under-served patients sooner?
Accountabilities:
  • RTSM Leadership and Delivery: Lead cross-functional, global study teams in the end-to-end set-up, delivery, maintenance, and archival of RTSM as the subject matter expert, ensuring systems are delivered to study timelines and needs.
  • Vendor Partnership and Standards: Coordinate and manage the RTSM vendor to deliver against timelines and standards in line with regulatory requirements; drive the implementation of RTSM standards and best practices; contribute to internal governance and vendor oversight.
  • User Acceptance and Quality: Plan and execute UAT, including authoring test plans, coordinating vendor support, and preparing study teams, to ensure right-first-time deployments and continuous monitoring.
  • Issue Management and Escalation: Serve as the study-level point of escalation for RTSM issues and ensure effective and timely resolution through established pathways.
  • Documentation and Budget Stewardship: Own required documentation as defined in the TMF and the team playbook; manage RFP processes and study-level RTSM budgets to ensure clarity, control, and value.
  • Continuous Improvement and Innovation: Participate in and lead improvement initiatives focused on RTSM; identify, assess, and help onboard best-in-class RTSM solutions to strengthen clinical supply operations.
  • Compliance and Inspection Readiness: Support audits and regulatory inspections; uphold blinding controls and data integrity across study operations to meet GxP and regulatory expectations.

Essential Skills/Experience:
  • Minimum of three to five years of experience in the biopharmaceutical industry with focus on RTSM study support.
  • End-to-end RTSM systems experience including set-up, implementation, and closeout of RTSM systems as well as issue management and vendor oversight.
  • Experience with various trial/study designs across different therapeutic areas and the operational knowledge of maintaining blinding controls and data integrity.
  • Strong understanding of RTSM, GCP, GMP and applicable regulatory requirements.
  • Demonstrated project management and process improvement skills including excellent planning, organizational, and analytical skills.
  • The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to: use a computer; engage in communications via phone, video, and electronic messaging; problem solve; engage in complex and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

Desirable Skills/Experience:
  • 5+ years of RTSM experience within biopharma industry with at least 3 years of managing complex studies and/or projects
  • Bachelor's degree, MBA, or equivalent level of experience
  • Business process mapping experience preferred
  • Excellent written and verbal skills and strong interpersonal skills
  • High level of proficiency in MS Office software including: Word, Excel, Outlook, Visio, and PowerPoint

The annual base pay (or hourly rate of compensation) for this position ranges from 138,392.80 - 207,589.20 USD Annual (80% - 120%). Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Why AstraZeneca:
Here, science meets urgency to change what's possible for people with rare and devastating conditions. You will work shoulder-to-shoulder with experts in clinical operations, supply chain, data, and quality-bringing unexpected teams together to spark bold ideas and scale them across a growing portfolio. We combine the autonomy and pace of a biotech with the reach and resources of a global biopharma, so your best thinking moves quickly from concept to impact. We value kindness alongside ambition, and we invest in your development so you can lead systems that protect patients, strengthen data integrity, and accelerate access to life-changing medicines.
Call to Action:
Lead the RTSM journey that keeps trials moving and patients protected-submit your application to shape how we deliver tomorrow's medicines today.
Date Posted
29-Jun-2026
Closing Date
09-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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