Senior Data Team Lead

EPM Scientific

$120K — $160K *
US-AnywhereRemote in New Mexico, US
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in health, biological, clinical, or mathematical sciences.
  • 10+ years of clinical data management experience.
  • 7+ years as an independent lead on global trials.
  • Experience managing trials with 1,000+ patients through full data management lifecycle.
  • Deep knowledge of CDM processes and regulatory standards.
  • Track record in client negotiations and bid defense meetings.
  • Familiarity with medical terminology, pharmacology, anatomy, and physiology.
  • Strong communication and leadership skills.

Responsibilities

  • Serve as the primary contact for clients on data management deliverables.
  • Lead multiple large-scale global studies or programs of studies.
  • Negotiate timelines, budgets, processes, and resources with clients.
  • Train and develop junior data management staff.
  • Oversee service delivery, milestone tracking, and quality assurance.
  • Manage project budgets, SOWs, and financial reporting.
  • Support RFPs, bid defenses, and pricing discussions.
  • Drive process improvements and participate in best practice initiatives.
  • Ensure compliance with GCP, regulatory guidelines, SOPs, and internal policies.

Benefits

  • Fully remote work opportunity within the U.S.
  • Participation in competitive annual incentive bonus structure.
Full Job Description
Senior Data Team Lead - Remote (US)
Global CRO - Full-Time

A leading global clinical research organization is seeking a Senior Data Team Lead to independently manage the end-to-end delivery of data management services across single and multi-service clinical trials. This role ensures high-quality, timely, and budget-aligned deliverables that meet customer expectations. The successful candidate will provide strategic leadership in project planning, execution, and close-out, while also mentoring junior team members and serving as a subject matter expert in clinical data management.

Key Responsibilities
  • Act as the primary point of contact for clients on data management deliverables.
  • Lead multiple large-scale global studies or programs of studies.
  • Negotiate directly with clients on timelines, budgets, processes, and resources.
  • Provide training and development to junior data management staff.
  • Oversee service delivery, milestone tracking, and quality assurance.
  • Manage budgets, SOWs, and financial reporting for assigned projects.
  • Support RFPs, bid defenses, and pricing discussions.
  • Drive process improvements and contribute to best practice initiatives.
  • Ensure compliance with GCP, regulatory guidelines, SOPs, and internal policies.

Qualifications
  • Bachelor's degree in health, biological, clinical, or mathematical sciences.
  • Minimum 10 years of clinical data management experience.
  • At least 7 years as an independent lead on global trials.
  • Proven ability to manage large trials (1,000+ patients) through full DM lifecycle.
  • Strong knowledge of CDM processes, regulatory standards, and therapeutic areas.
  • Experience in client negotiations and bid defense meetings.
  • Familiarity with medical terminology, pharmacology, anatomy, and physiology.
  • Excellent communication and leadership skills.

Location & Compensation
  • Remote (U.S)
  • Competitive salary range with annual incentive bonus.

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