Senior Director, TMF Services

TransPerfect

United States

On-site

USD 180,000 - 240,000

Full time

14 days+
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Job summary

LMK seeks a Senior Director for TMF Services to lead end-to-end TMF strategy, delivery, and growth across a global client base. The role partners with executives to set plans, grow revenue, and ensure top-tier TMF quality and inspection readiness.

You will drive profitability, oversee TMF platforms, and champion AI-enabled productivity while building cross-functional teams and strong senior client relationships. Travel as required to support strategic initiatives.

Qualifications

  • Bachelor's degree in life sciences or related field.
  • 12+ years in clinical operations, TMF, or clinical records management.
  • 10+ years of supervisory/management experience.
  • Deep knowledge of TMF strategy and eTMF platforms.
  • Strong knowledge of ICH E6(R2/R3), FDA 21 CFR Part 11, EMA TMF guidelines.
  • Proven ability to lead, scale teams, and manage client relationships.

Responsibilities

  • Partner with executive leadership to develop annual business plans, revenue targets, and service line roadmap.
  • Own Profit & Loss accountability for the TMF Services division, driving profitability through efficient delivery and pricing.
  • Lead adoption of AI technologies, automation, and digital tools to enhance productivity and outcomes.
  • Establish scalable delivery frameworks and quality standards across client engagements.
  • Monitor industry trends and translate insights into service improvements.
  • Build trusted advisor relationships with client stakeholders at the director and C-suite level.
  • Recruit, develop, and lead a high-performing team.

Skills

Strategic leadership
P&L management
Client relationship management
AI-enabled productivity
Cross-functional collaboration
Public speaking
Travel readiness

Education

Bachelor's degree or equivalent in life sciences

Tools

Veeva Vault
TMF platforms

Job description

Summary

The Senior Director, TMF Services is a senior leadership role responsible for the end-to-end management and strategic direction of the TMF Services division, overseeing service delivery, operational growth, and the continuous expansion of service offerings. The Senior Director will lead the strategic growth, operational excellence, and delivery of LMK's Trial Master File (TMF) services while building strong relationships across LMK, TransPerfect, and its global client base. Serving as a visible market presence and internal champion, this role drives operational excellence, AI-enabled productivity, and client success across the division. The Senior Director works cross-functionally with internal stakeholders and external clients to ensure the highest standards of delivery while positioning the LMK’s TMF Services division for sustained commercial growth.

Responsibilities
  • Partner with executive leadership to develop annual business plans, revenue targets, and service line roadmap.
  • Support business development to identify, pursue, and close new business opportunities including new client relationships, expanded scopes of work, and strategic partnerships.
  • Own Profit & Loss (P&L) accountability for the divisions TMF Services practice, driving profitability through efficient delivery models and pricing strategy.
  • Continuously evaluate and implement best-in-class tools and workflows for eTMF management, TMF record quality, and inspection readiness.
  • Establish scalable delivery frameworks and quality standards across client engagements.
  • Monitor industry trends (regulatory guidance, technology evolution, competitive landscape) and translate insights into service improvements.
  • Revise, implement and monitor departmental compliance with SOPs.
  • Champion the adoption of AI technologies, automation, and digital tools to enhance team productivity and client outcomes.
  • Serve as an executive sponsor for key client accounts, ensuring high levels of satisfaction, retention, and growth.
  • Oversee the successful delivery of the TMF Services portfolio, ensuring projects meet quality, timeline, budget, and compliance objectives.
  • Build trusted advisor relationships with client stakeholders at the director and C-suite level.
  • Ensure team members meet departmental and project productivity and quality metrics by efficient execution of their project in line with project plan.
  • Serve as a visible spokesperson and subject matter expert for the company in the eTMF and clinical operations space.
  • Represent the organization as a thought leader and subject matter expert through industry conferences, publications, webinars, and professional networks.
  • Build and maintain a strong external network with sponsors, CROs, technology vendors, and industry associations.
  • Recruit, develop, and lead a high-performing team while fostering a culture of accountability, collaboration, and continuous improvement.
  • Collaborate cross-functionally with commercial, technology, and operational teams to achieve strategic business objectives.
  • Complete all other tasks deemed appropriate for the role as assigned by the manager/supervisor.
Qualifications
  • Minimum Bachelor's degree or equivalent in life sciences, health sciences, or related field.
  • At least 12 years of progressive experience in clinical operations, TMF, or clinical records management within a CRO, sponsor company, or clinical services provider.
  • Minimum of 10 years of supervisory/management experience.
  • Strong understanding of clinical trial processes and clinical records management operations.
  • Proven experience presenting, speaking, or publishing in industry forums and professional settings.
  • Demonstrated success in leading and scaling teams in fast-paced, client-facing environments.
  • Demonstrated expertise in Trial Master File (TMF) strategy, eTMF platforms (e.g., Veeva Vault, TI, Wingspan, Medidata etc.), and supporting TMF inspection readiness.
  • Strong knowledge of applicable regulations and guidance: ICH E6(R2/R3), FDA 21 CFR Part 11, EMA TMF guidelines, CDISC TMF Reference Model.
  • Strong understanding of drug development and clinical trials operations.
  • Proven ability to navigate ambiguity and successfully build and scale processes, teams, and service offerings.
  • Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint). Outstanding verbal and written and interpersonal communication skills, with strong active listening abilities.
  • Strong analytical, problem-solving, and critical-thinking skills.
  • Ability to work effectively in a global, cross-functional environment with internal and external stakeholders.
  • Willingness to travel as required.
Desired Business Skills And Experience
  • Proven track record of business development and/or account growth in a services environment.
  • Active involvement in industry organizations (CDISC TMF Reference Model, etc.).
  • Experience evaluating and implementing AI/ML tools or automation within clinical workflows.
  • Prior P&L ownership or practice management experience within a boutique or mid-size services organization.
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