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Rtsm Project Manager Jobs (NOW HIRING)

UNC-Chapel Hill

HRSA Research Assistant

Chapel Hill, NC · Hybrid

$35 - $40/hr

Position Summary The Research Assistant (RA) supports research, evaluation, and project management ... RTSM, RTMB) and BHWRC MOUD study. Working Conditions * Office and hybrid work environment.

Merck & Co.

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 ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

... RTSM). * Perform post go-live changes (database modifications) based on updated requirement ... Maintain database design timelines and promote good project management practices. * Assist Clinical ...

Everest Clinical Research Services Inc.

... RTSM). * Perform post go-live changes (database modifications) based on updated requirement ... Maintain database design timelines and promote good project management practices. * Assist Clinical ...

Doist

Manager, Clinical Supply Operations

Bothell, WA · On-site

$144K - $169K/yr

... may support a wide range of projects, including biologics and small molecule programs ... Experience with IRT/RTSM systems supporting inventory and supply management functionality . * Close ...

MSD Malaysia

$173K - $272K/yr

Understanding of ERP systems (SAP), RTSM/IRT systems, or advanced data platforms is highly ... Professional certifications in project/product management (e.g., PMP, PMI-ACP, Certified Scrum ...

OCUGEN OPCO INC

TMF Lead

Malvern, PA · On-site

$32.75 - $45/hr

Develop and maintain TMF management plans, filing strategies, and Expected Document List (EDL ... Additional tasks and projects as requested. * Bachelor's degree in life sciences or a related field ...

Ocugen Inc

TMF Lead

Malvern, PA · On-site

$32.75 - $45/hr

Develop and maintain TMF management plans, filing strategies, and Expected Document List (EDL ... Additional tasks and projects as requested. * Bachelor's degree in life sciences or a related field ...

Ocugen Opco Inc

TMF Lead

Malvern, AR · On-site

$29.25 - $40/hr

Develop and maintain TMF management plans, filing strategies, and Expected Document List (EDL ... Additional tasks and projects as requested.Bachelor's degree in life sciences or a related field ...

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Rtsm Project Manager information

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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.

Senior Specialist, Clinical Supply Chain (IRT/RTSM)

San Diego, CA • On-site

Neurocrine Biosciences, Inc.
Biotechnology Research and Development • 1 - 5K employees
Learn more about Neurocrine Biosciences, Inc.external

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago

Job description

Who We Are:
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
About the Role:
Support Clinical Supply Chain activities, including but not limited to collaborating with internal stakeholders across Project Management, Clinical Operations, Quality Assurance, Regulatory Affairs, Technical Operations (Manufacturing and Analytical), Finance, and Legal, as well as external cGMP service providers.
Key responsibilities include serving as the Clinical Supply Chain subject matter expert (SME) for the configuration and management of Interactive Response Technology (IRT) systems; providing guidance to internal and external users on IRT systems and procedures; troubleshooting system and operational issues; managing system enhancements; and developing procedures and policies as needed.
The ideal candidate must have strong experience working with IRT providers and configuring IRT systems. The successful candidate will demonstrate strong organizational and project management skills, a thorough understanding of clinical study protocols, exceptional attention to detail, and an analytical, problem-solving mindset.
Additional responsibilities include supporting broader Clinical Supply Chain activities, such as managing budgets, contracts, and invoices; coordinating clinical and stability drug packaging and distribution; and managing overall clinical supply logistics. The role will also collaborate with external vendors involved in the planning, packaging, distribution, storage, and destruction of Clinical Trial Materials (CTM).
Your Contributions (include, but are not limited to):
  • Support establishment, management and maintenance of IRTs
  • Serve as Clinical Supply Chain IRT SME in development and post system go-live
  • Participate in development meetings with IRT vendor and Clinical Study Team
  • Troubleshoot issues within IRT systems, addressing inquiries, investigating root causes and implementing appropriate solutions or escalation
  • Issue RFQs, set up and manage contracts, budgets and billing with qualified IRT Vendors
  • Support clinical studies in the planning and execution of drug product management activities
  • Support development and review of Clinical Trial Materials (CTM) forecasts based on clinical trial study protocols
  • Support packaging/labeling of CTM with approved cGMP vendors, based on approved demands, working with internal partners and systems, processing all drug dispositioning
  • Support maintenance of CTM inventory working with vendors to ensure accuracy of inventory systems
  • Other duties as assigned

Requirements:
  • Bachelor's degree supply chain, life sciences or related field AND 6+ years relevant experience in clinical supply chain, with a heavy experience working with IRTs, packaging and labeling and distribution
  • Demonstrated success working with and managing third-party vendors.
  • Strong understanding of cGMP supply chain
  • In depth knowledge of IRT System development, implementation and maintenance
  • Strong knowledge of clinical study tools (CTMS)
  • Broad understanding of packaging/labeling requirements
  • Ability to effectively work within a multidisciplinary team and manage multiple vendors
  • Understands key clinical supply chain business drivers
  • Has strong understanding of IRT processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areas
  • Proficient with tools and processes that support work conducted by functional area
  • Ability to work as part of a team; may train lower levels
  • Excellent computer skills, proficient in Microsoft Office programs
  • Strong communications, problem-solving, analytical thinking skills
  • Detail oriented yet can see broader picture for department
  • Ability to meet multiple deadlines, with a high degree of accuracy and efficiency
  • Well-organized, detail-oriented with strong written and verbal communication skills
  • Strong project management and interpersonal skills
  • Self-starter working with a sense of urgency and acting as a team player
  • Adaptability, flexibility, independence and resourcefulness with ability to work with changing timelines and willing to roll-up-sleeves in order to thrive in small company environment

#LI-LS1
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
The annual base salary we reasonably expect to pay is $110,800.00-$151,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 20% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

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