Senior Global Trial Manager

Posted 2 Days Ago
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Durham, NC
112K-187K Annually
Senior level
Healthtech
The Role
The Senior Global Trial Manager leads clinical trial delivery, ensuring compliance and managing clinical teams for large, multi-regional studies.
Summary Generated by Built In

We are seeking a Senior Global Trial Manager to join our team!

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

As a Global Trial Manager, you will play a crucial role in clinical trial delivery, leading clinical teams to bring new drugs to market faster. You will be responsible for the clinical delivery of large, multi-regional studies, ensuring compliance with regulatory, customer, and internal requirements.

What you’ll be doing:

  • Ensuring clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs.
  • Meeting project recruitment targets and develop appropriate recruitment strategies.
  • Contributing to project risk mitigation plans and manage clinical risks throughout the project lifecycle.
  • Ensuring clinical quality delivery by identifying quality standards, planning compliance measures, and managing clinical quality issues.
  • Managing clinical aspects of project finances, including Estimate at Completion (EAC), and identify additional service opportunities.
  • Leading clinical teams to deliver large, global trials and manage internal and external stakeholders.
  • Supporting milestone achievements and reporting to stakeholders as per project scope requirements.
  • Managing the clinical team at the project level, including resourcing, talent planning, and providing project-related training.

What we are looking for:

  • Bachelor's Degree in health care or other scientific discipline.
  • 7 years of clinical research/monitoring experience or an equivalent combination of education, training, and experience.
  • Consolidated knowledge of project management practices and terminology.
  • Good knowledge of applicable clinical research regulatory requirements (GCP, ICH guidelines).
  • Other Equivalent combination of education, training, and experience may be accepted in lieu of degree.

The knowledge, skills, and abilities needed for this role:

  • Strong written and verbal communication skills, including good command of the English language.
  • Problem-solving skills and the ability to handle conflicting priorities.
  • Attention to detail and accuracy in work, with a results-oriented approach.
  • Good influencing, negotiation, judgment, and decision-making skills, with effective mentoring and training abilities.

What we offer you:

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental, emotional, financial, and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

To learn more about our benefits, visit https://jobs.iqvia.com/benefits.

If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $112,000.00 - $186,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Top Skills

Clinical Research Regulations
Project Management
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The Company
Bangalore, Karnataka
61,500 Employees
On-site Workplace
Year Founded: 2016

What We Do

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.

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