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Senior Global Trial Manager

7+ years
$93,100 – $232,800 per year
10 Oct. 16, 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

Position: Senior Global Trial Manager

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


About IQVIA

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, enabling faster development and commercialization of innovative treatments to improve patient outcomes worldwide.

IQVIA is committed to diversity, inclusion, and employee well-being, offering integrated benefits to support physical, mental, emotional, financial, and social health.
🔗 Learn more: https://jobs.iqvia.com
🔗 Benefits: https://jobs.iqvia.com/benefits


Position Overview

The Senior Global Trial Manager leads clinical teams to deliver large, multi-regional trials, ensuring regulatory compliance, customer satisfaction, and internal quality standards. The role involves overseeing clinical delivery, managing risks, monitoring project finances, and coordinating stakeholders globally.

Travel Requirement: Up to 25%


Key Responsibilities

1. Clinical Trial Delivery

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs.

  • Meet project recruitment targets and develop recruitment strategies.

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

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

2. Project Financials & Oversight

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

  • Identify opportunities for additional services or revenue.

3. Team Leadership & Stakeholder Management

  • Lead clinical teams for large, global trials.

  • Manage internal and external stakeholders.

  • Support milestone achievements and provide reporting per project scope.

  • Manage project-level resourcing, talent planning, and training.


Qualifications

Education:

  • Bachelor’s degree in Healthcare or a scientific discipline (or equivalent combination of education, training, and experience).

Experience:

  • 7 years of clinical research/monitoring experience.

  • Knowledge of project management practices and terminology.

  • Understanding of clinical research regulatory requirements (GCP, ICH guidelines).

Skills & Abilities:

  • Strong written and verbal communication skills, including proficiency in English.

  • Problem-solving and ability to handle conflicting priorities.

  • Attention to detail and accuracy in work, with a results-oriented approach.

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

  • Effective mentoring and training capabilities.


Compensation & Benefits

  • Base pay range: $93,100 – $232,800 per year (annualized)

  • Actual pay varies based on experience, qualifications, location, and schedule.

  • Incentives, bonuses, and a range of health and welfare benefits may also be offered.


Equal Opportunity Employer

IQVIA considers all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected status.


📩 Apply Now: IQVIA Careers – Senior Global Trial Manager