---
title: 'Senior Director, Data Management Systems at IMVT Corporation'
canonical: 'https://feeny.ai/job/senior-director-data-management-systems-imvt-corporation-remote-bw7zc2r5bz1x'
type: 'job'
last_seen: '2026-09-11'
---

# Senior Director, Data Management Systems at IMVT Corporation

- **Company:** IMVT Corporation
- **Location:** Remote
- **Compensation:** $260k–$290k
- **Work type:** remote
- **Posted:** 2026-08-19
- **Last confirmed live:** 2026-09-11
- **Apply:** https://job-boards.greenhouse.io/imvtcorporation/jobs/6147255004

## Job description

Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.

Organizational Overview:

Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases.

The Role:

Reporting to the Vice President, Data Management, this position is responsible for providing strategic and operational leadership over the clinical data technology ecosystem, including eCOA/ePRO platforms, eDiary solutions, Medidata Rave (EDC), and Elluminate. This role is not directly responsible for hands-on clinical data management activities (e.g., data cleaning, query resolution, database lock); rather, it requires a strong clinical data management background to inform sound systems strategy, oversee system governance, and lead a team responsible for platform architecture, configuration, integration, and lifecycle management. The ideal candidate understands data management processes deeply enough to translate them into scalable, well-governed technology solutions, and brings proven experience leading systems teams. Serves as a key member of the Data Management Leadership Team, supporting cross-functional team needs and oversees the management of system related enhancements to support study deliverables. Interfaces with CROs and is responsible for managing internal Data Management team members.

Key Responsibilities:

Leadership & Management

- Lead, mentor, and develop a team of clinical trial solutions personnel
- Set systems strategy, roadmap, and performance metrics; conduct performance reviews and support career development.
- Manage systems related budget, resourcing, vendor contracts, and staffing plans across concurrent systems and study portfolios.
- Serve as a key member of the clinical data management leadership team, representing clinical systems in cross-functional governance forums.
- Partner with (but do not directly own) the data management operations team and vendors, ensuring systems strategy aligns with DM process needs.

Clinical Systems Strategy & Governance

- Own the enterprise strategy, roadmap, and governance model for core clinical data systems, including:
- eCOA / ePRO platforms (patient/clinician-reported outcomes)
- eDiary systems
- Medidata Rave EDC
- Elluminate (data review, aggregation, and analytics platform)
- Define and maintain system governance frameworks: access management, role-based permissions, change control, and version control across platforms.
- Establish standards for system configuration, study build templates, and reusable libraries to drive consistency and efficiency across studies.
- Lead vendor management and contract oversight for all clinical systems vendors, including SLA definition, performance monitoring, and renewal/negotiation strategy.
- Own system-related budget planning, licensing decisions, and total cost of ownership analysis.

System Implementation & Lifecycle Management

- Lead selection, evaluation, and implementation of new clinical systems and platform upgrades, including RFP processes and vendor due diligence.
- Oversee computer system validation (CSV/CSA) activities, ensuring systems meet 21 CFR Part 11, GxP, and data integrity requirements.
- Direct system configuration, build, and testing activities for EDC, eCOA, eDiary, and Elluminate environments.
- Manage the end-to-end lifecycle of clinical systems: onboarding, ongoing maintenance, periodic review, upgrades, and decommissioning/retirement/data archival.
- Establish and maintain disaster recovery, business continuity, and system uptime/performance standards in partnership with IT.

Integration & Interoperability

- Lead architecture and oversight of system integrations (e.g., EDC-to-eCOA, EDC-to-Elluminate, EDC-to-IRT/RTSM/safety databases) to ensure seamless, accurate, and timely data flow.
- Partner with IT/technical teams to define data integration specifications, API/interface requirements, and data mapping standards.
- Troubleshoot and resolve systemic/integration-level issues, distinguishing systems-level root causes from data management process issues.
- Drive adoption of automation, AI-enabled tools, and dashboarding/analytics capabilities to improve data flow visibility and reduce manual effort.

Compliance, Quality & Risk

- Ensure clinical systems remain inspection-ready at all times; serve as the systems SME during regulatory inspections and audits.
- Maintain SOPs, validation documentation, and system-level quality standards in partnership with Quality Assurance.
- Monitor emerging regulatory guidance (e.g., FDA, EMA, ICH E6(R3)) related to clinical technology and data integrity, and proactively adapt systems strategy accordingly.
- Own risk assessments related to system changes, upgrades, and vendor transitions.

Cross-Functional Collaboration

- Serve as the primary systems liaison to Clinical Data Management, Biostatistics, Clinical Operations, Clinical Development, Regulatory, Quality, and IT.
- Provide systems and technology input into protocol development, study design feasibility, and technology selection at the program level.
- Educate and train clinical data management and cross functional staff on system capabilities, updates, and best practices.

Required Qualifications

- Bachelor's degree in life sciences, health information, computer science, or related field (advanced degree preferred).
- 15+ years of progressive experience in clinical data management and/or clinical data systems within pharmaceutical, biotech, or CRO environments.
- Strong foundational background in clinical data management (data cleaning, query management, database lock, DM planning) — this role oversees systems, not day-to-day data management operations, but requires fluency in DM processes to inform systems decisions.
- 5+ years of people management experience, including managing managers or system-focused teams.
- Demonstrated experience owning or administering:
- eCOA/ePRO systems
- eDiary platforms
- Medidata Rave EDC
- Elluminate
- Strong knowledge of system validation (CSV/CSA), 21 CFR Part 11, ICH-GCP, and global regulatory requirements governing clinical data systems.
- Proven track record leading system implementations, upgrades, integrations, and vendor management.
- Experience supporting regulatory inspections and audits related to clinical systems and data integrity.

## Preferred Qualifications

- Experience across multiple therapeutic areas and trial phases (I–IV).
- Familiarity with additional clinical technologies (e.g., IRT/RTSM, CTMS, safety databases, eTMF).
- Experience with system integration architecture, APIs, and data pipeline/interface design.
- Certification in clinical data management (e.g., CCDM), IT/systems (e.g., ITIL), or project management (e.g., PMP).
- Experience with computer system validation methodologies and audit trail/data integrity frameworks.

## Skills & Competencies

- Strategic, technology-forward thinking paired with strong operational execution.
- Deep understanding of clinical data management principles, applied through a systems and governance lens.
- Excellent people leadership, coaching, and team-building skills.
- Strong vendor management, negotiation, and contract oversight capabilities.
- Ability to translate business/process needs into scalable technical solutions.
- Excellent written and verbal communication skills, including with technical and non-technical stakeholders.
- Comfortable operating in a fast-paced, matrixed organization.

Work Environment:

- Remote-based
- Dynamic, interactive, fast-paced, and entrepreneurial environment
- Domestic or international travel are required (10-20%)

Salary range for posting $260,000—$290,000 USD

Compensation is based on a number of factors, including market location, and may vary depending on job-related knowledge, skills, and experience. Equity and other forms of compensation may be provided as part of a total compensation package, in addition to a full range of medical, dental, vision, 401k, and other benefits, including unlimited paid time off and parental leave.

## About IMVT Corporation

## Company Overview
- **One-liner**: A clinical-stage immunology company developing innovative anti-FcRn therapies to enable normal lives for people with autoimmune diseases.
- **Entity Type**: Public (Nasdaq: IMVT)
- **Headquarters**: Durham, North Carolina, United States
- **Founded**: Not publicly available
- **Founders**: Not publicly available

## Core Business
- **Primary industry**: Biotechnology / Autoimmune disease therapeutics
- **Target customers**: Patients with IgG-mediated autoimmune diseases; healthcare providers; payers (B2B/B2C mix via prescription drugs)
- **Mission or purpose statement**: “Dedicated to enabling normal lives for people with autoimmune diseases” [immunovant.com](https://www.immunovant.com/)

## Products & Services
- **[IMVT-1402 (imeroprubart)]**: A novel, fully human monoclonal antibody that targets FcRn to reduce pathogenic IgG autoantibodies. Designed as a subcutaneous injection with a simple autoinjector (YpsoMate®). In clinical development for six indications: Graves’ disease (GD), difficult-to-treat rheumatoid arthritis (D2T RA), myasthenia gravis (MG), chronic inflammatory demyelinating polyneuropathy (CIDP), Sjögren’s disease (SjD), and cutaneous lupus erythematosus (CLE). [10-K (2026)](https://www.immunovant.com/investors/sec-filings/all-sec-filings/content/0001764013-26-000064/0001764013-26-000064.pdf)
- **[Batoclimab (first-generation anti-FcRn)]**: Development discontinued across all indications after Phase 3 TED trials did not meet primary endpoints; learnings inform IMVT-1402 program. [10-K (2026)](https://www.immunovant.com/investors/sec-filings/all-sec-filings/content/0001764013-26-000064/0001764013-26-000064.pdf)

## Market Standing
- **Valuation/Market Cap**: Not disclosed in available sources (publicly traded on Nasdaq; refer to real-time market data).
- **Key Metric**: Clinical-stage company with no approved products or revenue; total funding and operating expenses are detailed in SEC filings but not summarized here.
- **Notable Investors/Partners**: HanAll Biopharma (collaboration on anti-FcRn antibodies); Ypsomed AG (auto-injector YpsoMate®). [10-K (2026)](https://www.immunovant.com/investors/sec-filings/all-sec-filings/content/0001764013-26-000064/0001764013-26-000064.pdf)
- **Growth Signals**: Six ongoing clinical programs (including potentially registrational trials); deep IgG reductions (~80% with weekly 600 mg IMVT-1402) suggesting best-in-class potential; Phase 1 safety data showing no/minimal albumin reduction or LDL cholesterol increases. [10-K (2026)](https://www.immunovant.com/investors/sec-filings/all-sec-filings/content/0001764013-26-000064/0001764013-26-000064.pdf)

## Competitive Advantages
- **Potential best-in-class efficacy**: IMVT-1402 achieves deeper IgG reductions than competitor anti-FcRn antibodies, correlating with improved clinical outcomes.
- **Favorable safety profile**: No or minimal off-target effects on albumin and LDL cholesterol, unlike some FcRn inhibitors.
- **Convenient administration**: Self-administered subcutaneous autoinjector (YpsoMate®) expected at launch, improving patient adherence.
- **Broad pipeline**: Six indications in development across endocrinology, rheumatology, neurology, and dermatology, with potential for more.

## Strategic Focus
- Execute pivotal trials for IMVT-1402 in GD, D2T RA, MG, CIDP, SjD, and CLE.
- Leverage learnings from batoclimab program to accelerate IMVT-1402 development.
- Plan to assess new indications for IMVT-1402 beyond the initial six.
- Continue to build commercial capabilities for eventual launch. [10-K (2026)](https://www.immunovant.com/investors/sec-filings/all-sec-filings/content/0001764013-26-000064/0001764013-26-000064.pdf)

## Why Work Here
- **Culture**: Emphasizes “Hire and Retain Only the Very Best,” “One Team, Shared Success,” “Ownership Mentality,” and “Patients Are Waiting” – a mission-driven, high-performance environment. [About Us](https://www.immunovant.com/about-us)
- **Remote/Hybrid Policy**: Job listings show a mix of remote and hybrid roles (e.g., “Remote” for many positions, “Hybrid - NYC” for commercial roles). [Careers](https://www.immunovant.com/join-us/explore-careers)
- **Notable Perks**: Merit-based recognition, focus on impact and results, creative problem-solving encouraged. [About Us](https://www.immunovant.com/about-us)
- **Engineering/Science Culture**: Clinical-stage biotech with cutting-edge FcRn technology; opportunities in clinical development, biometrics, quality assurance, and commercial roles. [Careers](https://www.immunovant.com/join-us/explore-careers)

## Sources
1. [Immunovant Corporate Website](https://www.immunovant.com/)
2. [About Us – Values and Culture](https://www.immunovant.com/about-us)
3. [Company Information – Investor Relations](https://www.immunovant.com/investors/company-information)
4. [Explore Careers – Job Listings](https://www.immunovant.com/join-us/explore-careers)
5. [10-K SEC Filing (May 20, 2026)](https://www.immunovant.com/investors/sec-filings/all-sec-filings/content/0001764013-26-000064/0001764013-26-000064.pdf)

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