Job Details

Senior Data Teal Lead

6049
  • $Competitive
  • Fully Remote - US, North Carolina, United States
  • Permanent

Senior Lead Clinical Data Manager | Remote – US | Permanent |

Are you an experienced Clinical Data Manager looking to step into a leadership role with global impact? We’re seeking a Senior Lead Clinical Data Manager to oversee the end-to-end delivery of Data Management (DM) services for complex clinical studies and programs. This is a fully remote opportunity, open across the US, offering the chance to shape data strategy and execution within a world-class environment.

What you’ll be doing:

  • Lead data management delivery across single or multi-service projects, ensuring quality, timelines, and customer satisfaction.
  • Act as the primary client contact for DM deliverables, building strong relationships and driving successful outcomes.
  • Provide leadership and vision in project planning, execution, close-out, financial oversight, communications, and milestone delivery.
  • Serve as Data Team Lead (DTL), Program Lead, or SME within CDM.
  • Mentor and train junior staff, sharing best practices and lessons learned.
  • Support business development through RFP reviews, bid defenses, and solution proposals.
  • Manage DM project life cycles, from planning to close-out, across multiple studies/programs.
  • Develop and maintain Data Management Plans (DMPs), ensuring compliance with GCP, SOPs, and regulatory guidelines.
  • Ensure proactive quality management, issue resolution, and process improvements.
  • Oversee project financials, including SOW/budget management, financial tracking, and invoicing.
  • Collaborate with internal teams and external vendors on SAE reconciliation, lab/vendor data integration, and compliance.
  • Represent the company at professional conferences, workshops, and industry forums.

What you’ll need:

  • Bachelor’s degree (or equivalent) in life sciences, health, biological, mathematical sciences, or related field.
  • 10+ years’ direct Data Management experience, including 5- 7 years as a CDM project lead.
  • Demonstrated success in leading full DM life cycles across multiple studies/programs.
  • Strong knowledge of medical terminology, pharmacology, anatomy/physiology, GCP, and regulatory guidelines.
  • Excellent project management, communication, and client-facing skills.
  • Experience negotiating with customers and managing out-of-scope tasks/change orders.
  • Ability to mentor, influence, and drive process improvements within teams.

What’s in it for you:

  • Fully remote flexibility across the US.
  • Opportunity to lead global projects and collaborate with top sponsors.
  • Work in an environment that values innovation, quality, and continuous improvement.
  • Contribute to meaningful advances in clinical drug development.

What to do next:

If this opportunity aligns with your experience and career goals, please apply now with your CV.

Jo Fornaciari Principal Consultant | Biometrics

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