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Program Manager

Green Life Science
Department:Project Management
Type:REMOTE
Region:USA
Location:United States
Experience:Mid-Senior level
Estimated Salary:$120,000 - $180,000
Skills:
CLINICAL OPERATIONSPHASE 3 CLINICAL TRIALSGLOBAL CLINICAL DEVELOPMENTCRO MANAGEMENTVENDOR MANAGEMENTGCP COMPLIANCEICH GUIDELINESBUDGET MANAGEMENTSTAKEHOLDER MANAGEMENTRISK MANAGEMENT
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Job Description

Posted on: March 13, 2026

Program Manager – Clinical Operations (Phase 3 Cardiovascular)

We are currently partnered with an innovative clinical-stage biotechnology company developing targeted therapies for serious diseases. They are seeking an experienced Program Manager (Clinical Operations) to support and lead a late-stage global clinical development program in cardiovascular indication.

📍 Location: Preference for US East Coast, though candidates across the US or Europe will also be considered.

The Role

The Program Manager will hold end-to-end operational responsibility for a global Phase 3 clinical development program in a cardiovascular indication.

This role requires strong late-stage clinical operations expertise, a hands-on execution mindset, and the ability to manage complex global studies in a fast-paced biotech environment.

Key Responsibilities

  • Lead the operational delivery of a global Phase 3 clinical program
  • Oversee study planning, execution, and delivery, ensuring timelines, quality, and budget adherence
  • Manage and oversee clinical sites, CROs, vendors, and central service providers
  • Oversee contracts, budgets, forecasts, timelines, and study deliverables
  • Coordinate global clinical trial activities across multiple regions
  • Ensure compliance with GCP and ICH guidelines and maintain inspection readiness
  • Proactively manage operational risks and cross-functional dependencies
  • Serve as a key operational partner to Clinical, Medical, and Regulatory teams
  • Drive effective communication with internal stakeholders and external partners
  • Operate successfully within a dynamic and collaborative biotech environment

Experience & Skills

  • 10+ years of clinical operations experience, including late-stage development
  • Demonstrated experience managing global Phase 3 clinical trials
  • Strong background working with CROs, vendors, and international investigator sites
  • Solid understanding of clinical trial operations, regulatory compliance, and inspection readiness
  • Strong organizational, planning, and stakeholder management skills
  • Ability to manage complexity and drive execution in fast-moving environments
  • Comfortable working hands-on while maintaining program-level oversight
  • Fluency in English (additional languages are a plus)
Originally posted on LinkedIn

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