Senior Clinical Trial Manager

Company: SoTalent Agency

  • Location: United States
  • Seniority: Senior
  • Employment type: Full-time
  • Posted: Yesterday
  • Offer language: English

Job description

Senior Clinical Trial Manager – Global Clinical Operations

Location: Philadelphia, PA, US

Employment Type: Full-time

Work Model: Remote

Salary: $145,600–$218,400/year

Overview

Senior Clinical Trial Manager responsible for leading global Phase I–IV clinical trials from planning through closeout. The role oversees study strategy, cross-functional execution, vendors, budgets, timelines, documentation, risk management and GCP compliance while providing operational leadership across global clinical teams.

Key Responsibilities

  • Lead planning, implementation and execution of global, multi-center Phase I–IV clinical trials.
  • Develop trial strategies, timelines, budgets, recruitment plans and risk mitigation plans.
  • Coordinate cross-functional study teams and lead trial-related meetings and working groups.
  • Provide operational oversight of external service providers and clinical vendors.
  • Manage vendor performance, financial spend, timelines and contractual deliverables.
  • Oversee Trial Master File (TMF) activities and essential trial documentation.
  • Review and approve protocols, informed consent forms, monitoring plans and Clinical Study Reports.
  • Support feasibility, study start-up, investigator selection and patient recruitment strategies.
  • Lead Investigator Meeting planning and delivery.
  • Identify and manage operational risks, issues and contingencies.
  • Provide study updates, risks and recommendations to senior leadership.
  • Serve as a clinical operations subject matter expert during audits and regulatory inspections.
  • Ensure trial activities comply with ICH-GCP, SOPs, regulatory requirements and study protocols.
  • Coordinate clinical supplies and investigational medicinal product shipment activities.
  • Support monitoring report review, data query processes and trial management systems.
  • Contribute to Clinical Operations and Global Clinical Development Operations initiatives.
  • Mentor and coach Clinical Research Associates, Global Study Managers and Global Study Associates.
  • Lead high-performing clinical trial teams and support resolution of complex study issues.

Requirements

  • 7+ years of clinical research experience, including global clinical trial management.
  • At least 3 years in clinical operations leadership.
  • Proven experience managing global, multi-center clinical trials.
  • Strong knowledge of clinical trial processes, ICH-GCP and regulatory requirements.
  • Experience with study start-up and regulatory planning.
  • Experience with CTMS, TMF and other clinical trial management systems.
  • Strong vendor, budget, timeline and risk management experience.
  • Excellent project management and organisational skills.
  • Strong stakeholder management, communication and influencing skills.
  • Bachelor’s degree in Life Sciences, Healthcare or related field, or equivalent experience.
  • Advanced degree preferred.
  • Proficiency in Microsoft Office.

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