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Job Description

Senior Global Trial Manager - Hybrid or Remote

Durham, Caroline du Nord R1453832

Durham, Caroline du Nord| Caroline du Nord

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Description du poste

We are seeking a Senior Global Trial Manager to join IQVIA Laboratories in Durham, NC in a hybrid or remote role.

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 Senior 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

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.https://jobs.iqvia.com/covid-19-vaccine-status

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.
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