Signant Health

General Manager Data Management Solutions - Operations

Signant Health  •  United States (Onsite)  •  2 hours 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, Data Management Solutions.

About the Role

The General Manager, Data Management Solutions owns the strategic direction, organizational leadership, and overall performance of Signant Health's Global Data Management function, encompassing RTSM, eCOA, sensors, and EDC operations. This leader holds full profit-and-loss (P&L), budget, and resource allocation accountability for the Data Management organization — including direct P&L ownership of the EDC business line — and sets the enterprise vision and multi-year roadmap for data management, ensuring Signant Health stays ahead of evolving CRO/Pharma industry demands, client expectations, and regulatory requirements. The General Manager also serves as Signant Health's foremost subject matter expert on clinical data management, representing the organization's capabilities to clients, prospects, and at industry conferences and forums, and works cross-functionally with Technical Delivery, Product/R&D, Commercial, and Project Management leadership to ensure data management strategy and service delivery support business growth and client commitments.

Key Responsibilities

  • P&L & Business Ownership: Own full profit-and-loss, budget, and resource allocation accountability for the Data Management function — including direct P&L ownership of the EDC business line — ensuring investments support strategic initiatives, scalability, and profitable growth across RTSM, eCOA, sensors, and EDC.
  • Strategy & Roadmap Leadership: Own the enterprise strategy and multi-year roadmap for Global Data Management, keeping pace with emerging technology and the evolving CRO/Pharma regulatory landscape.
  • Global Team Leadership: Provide strategic leadership, coaching, and development to build a high-performing, cross-functional Data Management organization, including hiring, retention, and succession planning for senior leaders.
  • Quality, Compliance & Audit Readiness: Set enterprise standards for data quality, GCP/regulatory compliance, and CDISC standards (e.g., SDTM, ADaM, CDASH) across CDMS/EDC platforms; lead the organization's audit and regulatory inspection readiness, serving as executive point of contact during FDA, EMA, and client audits.
  • Subject Matter Expertise & Client Engagement: Serve as Signant Health's foremost subject matter expert on clinical data management, representing the organization's capabilities to clients, prospects, and industry forums, and partnering with Commercial on strategic pursuits and client presentations.
  • Cross-Functional Collaboration: Partner closely with Technical Delivery, Product/R&D, Commercial, and Project Management leadership to ensure data management capabilities and service levels support client commitments and business growth.
  • Performance & Risk Governance: Own governance of Key Performance Indicators (KPIs) and Service Level Agreements (SLAs) across the Data Management organization, presenting performance results and strategy updates to executive leadership; set risk management and business continuity strategy supporting global clinical trial delivery.

What You'll Bring:

  • Bachelor's degree in a relevant field (Statistics, Computer Science, Life Sciences) or equivalent work experience; advanced degree preferred.
  • 15+ years of progressive experience in clinical data management within the CRO/Pharma or clinical trials industry, including 10+ years of senior people management experience leading multi-team or multi-site organizations.
  • Deep understanding of CRO/Pharma industry dynamics, client expectations, and the global regulatory environment (GCP, 21 CFR Part 11) governing clinical data management, including RTSM, eCOA, and Clinical Data, with proven experience successfully hosting regulatory inspections and audits (e.g., FDA, EMA).
  • Expert-level knowledge of Clinical Data Management Systems (CDMS) and Electronic Data Capture (EDC) platforms and comprehensive understanding of CDISC standards (SDTM, ADaM, CDASH).
  • Strong financial acumen, with proven experience owning full P&L (including for a product or business line such as EDC) or multi-million dollar budgets and resource planning for a global organization.
  • Strong executive communication and presentation skills, with proven ability to represent Data Management capabilities to clients, prospects, industry forums, and senior leadership, and to support business development and sales pursuits.

Nice to Have:

  • Advanced degree (MBA, MS) in a relevant field.
  • Experience working directly with CRO or Pharma clients in a service delivery or account leadership capacity.
  • Familiarity with computer system validation principles, quality systems, and industry trends in clinical data technology.
  • Experience representing an organization's data management capabilities to investors, partners, or at industry conferences and forums.

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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