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Senior Global Trial Manager

7+ years
$93,100.00 - $232,800.00
10 Oct. 4, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🏷️ Job Title: Senior Global Trial Manager

📍 Location: Durham, North Carolina (Home-based/Remote)
🕒 Employment Type: Full Time
🔢 Job ID: R1505413
📍 Additional Locations: North Carolina


🧭 Job Overview

The Senior Global Trial Manager leads clinical teams to deliver large, multi-regional studies, ensuring regulatory, customer, and internal compliance. This role focuses on clinical delivery, quality, and risk management, while overseeing project finances, resourcing, and stakeholder engagement.


⚙️ Key Responsibilities

Clinical Delivery

  • Ensure clinical delivery of assigned projects in compliance with GCP, ICH guidelines, customer contracts, and SOPs.

  • Achieve project recruitment targets and develop effective recruitment strategies.

  • Contribute to project risk mitigation plans and manage clinical risks throughout the project lifecycle.

  • Ensure clinical quality delivery by identifying standards, planning compliance measures, and managing quality issues.

Financial & Resource Management

  • Manage clinical aspects of project finances, including Estimate at Completion (EAC).

  • Identify additional service opportunities or out-of-scope work.

  • Oversee clinical team resourcing, talent planning, and project-related training.

Leadership & Collaboration

  • Lead clinical teams to deliver large, global trials.

  • Manage internal and external stakeholders effectively.

  • Support milestone achievement and report project progress to stakeholders.

  • Mentor and train team members, providing guidance on clinical delivery.

  • Travel up to 25% as required.


🎓 Qualifications & Requirements

Education

  • Bachelor’s Degree in Health Care or other scientific discipline.

  • Equivalent combination of education, training, and experience may be accepted in lieu of degree.

Experience

  • Minimum 7 years clinical research/monitoring experience or equivalent.

  • Consolidated knowledge of project management practices and terminology.

  • Strong knowledge of GCP, ICH, and regulatory requirements.

Skills & Competencies

  • Strong written and verbal communication skills in English.

  • Problem-solving ability and ability to handle conflicting priorities.

  • Attention to detail and results-oriented approach.

  • Influencing, negotiation, judgment, and decision-making skills.

  • Mentoring and training skills for team development.


🌍 About IQVIA

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence, accelerating the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.

🔗 Learn more: https://jobs.iqvia.com


⚖️ Equal Employment Opportunity

IQVIA provides equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.


💰 Compensation

  • Base Pay Range (Annualized): $93,100 – $232,800

  • Additional incentives, bonuses, and benefits may apply.