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Rtsm Project Manager Jobs (NOW HIRING)

Metasys

HP UD/UCMDB Consultants

Alexandria, VA · On-site

Proven implementation success with numerous fortune 500 clients 100s of successful projects across ... management policy Integrations o Integrate UCMDB with RTSM database for BSM/OMi o Integrate UCMDB ...

Merck Gruppe - MSD Sharp & Dohme

Understanding of ERP systems (SAP), RTSM/IRT systems, or advanced data platforms is highly ... Agile Project Management, Budget Development, Clinical Supply Chain Management, Clinical Trial ...

Kelly Services

Clinical Supply Manager

Rochester, NY · On-site

$47/hr

Collaborate with Clinical Ops and Data Management for RTSM system set-up. UAT testing. * Manage ... project management experience, given preference * Exemplary organizational and time management ...

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How much do rtsm project manager jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for rtsm project manager in the United States is $46.24, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $50.72 per hour, depending on experience, location, and employer.

What is an RTSM Project Manager?

An RTSM (Randomization and Trial Supply Management) Project Manager is responsible for overseeing the implementation and management of RTSM systems in clinical trials. These professionals coordinate between sponsors, vendors, and internal teams to ensure that randomization processes and supply logistics are executed accurately and efficiently. They play a critical role in planning, configuring, testing, and supporting RTSM solutions to meet study requirements, timelines, and regulatory standards. Their work ensures that clinical trial sites receive the correct study drug supplies on time and that participant randomization is conducted according to protocol.

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

To thrive as an RTSM (Randomization and Trial Supply Management) Project Manager, you need a solid understanding of clinical trials, project management principles, and regulatory requirements, often supported by a degree in life sciences or related fields. Familiarity with RTSM platforms, clinical trial management systems (CTMS), and project management tools like MS Project or Jira is typically required. Strong communication, problem-solving, and leadership skills help you manage cross-functional teams and client relationships effectively. These skills ensure the successful delivery of complex clinical trial projects, maintaining compliance and meeting sponsor expectations.

What are some common challenges faced by RTSM Project Managers when coordinating with cross-functional teams?

RTSM Project Managers often work closely with clinical, data management, and IT teams to deliver Randomization and Trial Supply Management solutions for clinical trials. A common challenge is ensuring clear communication between stakeholders with different technical backgrounds and priorities, which can lead to misaligned expectations or delays. Additionally, managing timelines and adapting to evolving protocol changes while maintaining system compliance requires strong organizational and problem-solving skills. Successful RTSM Project Managers proactively facilitate collaboration, clarify requirements, and anticipate potential issues to keep projects on track.

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

AspectRtsm Project ManagerRtsm Coordinator
CertificationsPMI PMP, Rtsm-specific trainingRtsm certification, relevant training
Work EnvironmentOversees multiple projects, strategic planningSupports project teams, handles day-to-day tasks
ResponsibilitiesProject planning, resource management, stakeholder communicationAssists with scheduling, documentation, coordination

The Rtsm Project Manager typically holds more strategic and leadership responsibilities, overseeing entire projects and managing teams. The Rtsm Coordinator focuses on supporting project execution through administrative and logistical tasks. Both roles require Rtsm-specific credentials and work within similar environments, but the Project Manager has a broader scope and decision-making authority.

What are popular job titles related to Rtsm Project Manager jobs?

For Rtsm Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Rtsm Project Manager job openings in the United States as of September 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $96,184 per year, or $46.2 per hour.

Manager, Clinical Supply Chain

Redwood City, CA • On-site

Revolution Medicines
See more jobs at Revolution Medicinesexternal

Full-time

Re-posted 2 days ago

Job description

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor-all in service of patients.
The Opportunity:
The Manager serves as the clinical supply chain lead for assigned clinical studies and ensure uninterrupted clinical trial supply. This position partners closely with Clinical Operations, product lead, Regulatory Affairs, Quality Assurance, Project Management, and external vendors to support the successful execution of global clinical studies while maintaining compliance, inspection readiness, and operational excellence.
Responsibilities:
  • Serve as the clinical supply lead for assigned study(s) and develop/manage the clinical supply Develop and execute comprehensive clinical supply strategies for global clinical development programs from Phase I through Phase III, ensuring alignment with program objectives, enrollment assumptions, manufacturing timelines, and regulatory requirements.
  • Lead demand forecasting, supply planning, inventory management, and scenario analysis to ensure continuous product availability while minimizing waste and supply risk.
  • Execute global packaging, labeling, and distribution, ensuring compliance with country-specific requirements and efficient supply to clinical sites worldwide.
  • Support IRT/RTSM systems, including development of user requirements, execution of user acceptance testing, implementation of supply strategies, change controls, and ongoing system maintenance.
  • Review and approve clinical supply chain documentation including clinical label text, batch records, pharmacy manuals, protocols. Support INDs, IMPDs, and other regulatory submissions as applicable.
  • Facilitate vendor selection, qualification, contracting, and performance management activities for packaging vendors, depots, logistics providers, comparator sourcing vendors, and other external partners.
  • Develop and implement risk management strategies to proactively identify and mitigate supply chain risks that could impact study timelines or patient enrollment.
  • Represent Clinical Supply Chain on cross-functional program teams and governance committees, providing strategic recommendations and decision-making support.
  • Develop and manage study level clinical supply budgets, vendor forecasts, and operational expenditures.
  • Facilitate continuous improvement initiatives and establish scalable processes, systems, and metrics to support organizational growth.
  • Participate in author, review, approve, and maintain SOPs, work instructions, and business processes related to clinical supply chain operations.

Required Skills, Experience and Education:
  • Bachelor's or Master's degree in Supply Chain, Life Sciences, Pharmacy, Engineering, or a related scientific discipline with a minimum of five years of relevant pharmaceutical or biotechnology industry experience. Demonstrated experience managing global clinical supply chains supporting Phase I through Phase III clinical trials is required.
  • Candidates must possess knowledge of clinical supply planning, forecasting, inventory management, packaging, labeling, distribution, and clinical logistics. Strong experience managing external vendors, depots, distribution centers, and logistics providers is essential.
  • The successful candidate will have a thorough understanding of GCP, GMP, GDP, ICH guidelines, and global regulatory requirements governing clinical trial materials. Strong leadership, communication, organizational, analytical, and project management skills are required, along with experience working effectively across complex cross-functional organizations.
  • Experience with IRT/RTSM systems, inventory management systems, ERP platforms, and clinical supply planning tools is required.

Preferred Skills:
  • Experience supporting oncology clinical development programs is preferred. Additional experience supporting late-stage development, comparator sourcing, combination therapy studies, commercial readiness activities, and global cold-chain distribution is highly desirable.
  • Experience implementing clinical supply systems, driving process improvements, and leading or mentoring supply chain professionals in a growing biotechnology environment is also preferred.

#LI-Hybrid #LI-CT1
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact privacy@revmed.com.
Base Pay Salary Range
$143,000-$178,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.
If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to careers@revmed.com so we can share these impersonations with our IT team for tracking and awareness.

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