Signant Health

General Manager RTSM & Study Supplies - Operations

Signant Health  •  United States (Onsite)  •  1 hour ago
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Job Description

About Signant Health

At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so better data leads to better decisions in healthcare. We embrace AI and advanced technologies to enhance every aspect of what we do, from data analysis to operational efficiency.

Our teams work at the intersection of science, technology, and patient experience, delivering digital solutions powered by AI innovation that make clinical trials more efficient, more accurate, and more accessible around the world. Trusted by leading pharmaceutical companies and CROs, our platforms and services support studies across more than 90 countries and have contributed to hundreds of new drug approvals.

If you are motivated by meaningful work, global impact, and innovation in clinical research and digital health — including the opportunity to work with cutting-edge AI technologies — you will find purpose and opportunity at Signant Health.

We have an immediate opening for a General Manager, RTSM & Study Supplies.

About the Role

The General Manager, RTSM & Study Supplies holds full profit-and-loss (P&L) accountability for the company's Randomization and Trial Supply Management (RTSM) solution and Study/Clinical Supplies business — including clinical supplies solutions, connected sensors, and devices used in clinical trials. This role leads global service delivery for the RTSM platform alongside end-to-end supply chain operations, including software implementations, fulfillment, returns, warehouse management, and patient/site support. The GM is accountable for both the commercial performance (revenue, margin, growth) and the operational execution (delivery quality, logistics, service levels) of the business unit and serves as the single point of executive accountability across technology delivery and physical supply chain operations.

Key Responsibilities

  1. P&L & Business Ownership: Own full profit-and-loss accountability for the RTSM and Study Supplies business unit, including revenue growth, gross margin, and operating expense management; develop the annual operating plan and pricing strategy; report business performance to executive leadership.
  2. Solution & Product Portfolio Leadership: Own the strategic roadmap and lifecycle for the RTSM platform, clinical supplies software, and connected sensors/devices portfolio; partner with Product Management and Engineering on investment priorities; ensure the portfolio remains compliant with applicable regulatory requirements (e.g., GxP, 21 CFR Part 11, data privacy).
  3. Global Service Delivery: Lead global delivery teams responsible for RTSM study builds, configuration, testing, and go-live support; ensure delivery quality, timeliness, and client satisfaction targets are met; standardize delivery processes to drive operational efficiency and scalability.
  4. Supply Chain & Logistics Operations: Oversee end-to-end clinical supplies operations, including forecasting, fulfillment, packaging, labeling, distribution, and returns/destruction; manage the global network of warehouses and depots, inventory, demand planning, and vendor/carrier relationships.
  5. Client & Site Support: Ensure global support operations for supplies and device-related client and site inquiries meet service-level targets; drive continuous improvement in support quality, responsiveness, and first-contact resolution.
  6. Team Leadership: Build, lead, and develop a global, cross-functional organization spanning delivery, supply chain/logistics, warehouse operations, and support functions; set organizational structure, staffing plans, and talent strategy; foster a culture of accountability, quality, and continuous improvement.
  7. Cross-Functional Collaboration: Partner with Sales on deal support, scoping, and pricing; collaborate with Regulatory, Quality, and Compliance on audit-readiness; work with IT/Engineering on device integration and platform reliability; partner with Finance on forecasting and margin improvement.

What You'll Bring:

  1. Bachelor's degree in business, life sciences, supply chain, engineering, or a related field; MBA or advanced degree preferred.
  2. 12+ years of progressive leadership experience in clinical trial technology, clinical supplies/logistics, or CRO/pharma operations, including at least 5 years in a P&L-owning role.
  3. Demonstrated experience managing global service delivery and/or supply chain/logistics operations, ideally within clinical trials, pharma, or medical device industries.
  4. Experience managing global, multi-site, or matrixed teams.
  5. Strong commercial acumen — budgeting, forecasting, pricing, and margin management.
  6. Working knowledge of GxP, GMP/GDP, and clinical trial regulatory requirements as they relate to supplies and technology.

Nice to Have:

  1. Prior experience at a CRO, clinical technology vendor, or clinical supplies/logistics provider.
  2. Experience with warehouse management systems (WMS), IRT platforms, and IoT/device connectivity.
  3. Track record of driving margin improvement and operational scaling in a global services business.

Why Signant Health?

At Signant Health, your work has real impact. Everything we build, support, and deliver helps advance clinical research and bring new treatments to patients faster — improving lives around the world. Our teams combine science, technology, and operational expertise to solve complex clinical trial challenges, and every role contributes to that mission.

We offer a collaborative, global environment where you can grow your career while working alongside experts across clinical, technology, data, and operations, with opportunities to learn, take ownership, and drive meaningful innovation — not just maintain the status quo.

If you are looking for purpose-driven work, smart colleagues, and the opportunity to help shape the future of clinical research and digital health, Signant Health is the place to do it.

At Signant Health, accepting difference isn't enough — we celebrate it, we support it, and we nurture it for the benefit of our team members, our clients, and our community. We are proud to be an equal opportunity workplace and an affirmative action employer, committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or veteran status. Prior to their start date, all new hires are required to be verified through a thorough background check and identity verification to confirm eligibility for employment.

Unsolicited resumes submitted by agencies or third-party recruiters directly to hiring managers or any Signant Health employee will not be considered and will not obligate Signant Health to any fees or terms associated with the submission.

Signant Health

About Signant Health

For 25+ years, Signant Health has been pioneering solutions and methodologies that propel clinical research programs toward regulatory success. Our approach combines deep scientific expertise with comprehensive eClinical solutions, enabling study teams capture reliable evidence while making trials more manageable for sites and more meaningful for patients.

From the smallest biotech running their first trial to global pharma sponsors and CROs launching pivotal, multinational studies, we're the partner who's been there before - supporting over 6,000 studies across 90+ countries, and contributing to 25% of recent FDA and EMA drug approvals.

Visit www.signanthealth.com to discover how we deliver Proof at the Speed of Life™.

Industry
IT & Software
Company Size
1,001-5,000 employees
Headquarters
Blue Bell, Pennsylvania
Year Founded
2000
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