Sr Global Trial Manager

hace 20 horas

Buenos Aires, Buenos Aires C.F., Argentina IQVIA A tiempo completo $120.000 - $180.000 al año

Are you prepared to be an IQVIAN?
IQVIA's mission is to accelerate innovation to help create a healthier world – and delivering on this ambition requires the right connections between our capabilities, expertise, and people. Every day, we work together to drive healthcare forward in ways both big and small, helping customers solve problems and improving patient outcomes. No matter your role, this is what it means to be an IQVIAN.

Join us a
Global Trial Manager
to be part in our team in Argentina or Mexico.

You will:

  • Participate in bid defense preparations. Attend bid defense presentations and lead the clinical delivery strategy for medium size and multiple country/region studies, in partnership with business development as needed.
  • Develop and maintain clinical project plans, including but not limited to clinical operations plan, recruitment and retention strategy plan, etc. to be incorporated into the integrated study management plan/project management plan.
  • Accountable for the clinical delivery (subject recruitment, site management, data integrity) per contract, ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
  • Ensure all appropriate subject/patient recruitment strategies are in place at the outset of the study to maximize subject/patient recruitment opportunities to achieve delivery according to contract, including, but not limited to, all outreach or digital offerings being explored and deployed.
  • Manage risks (positive and negative) which could impact on the clinical delivery of the project and determine contingencies. Partner with functional leaders in problem solving and resolution efforts.

What do you need to have?

  • Advanced degree or equivalent education/degree in life science/healthcare recommended.
  • 7 years clinical research/monitoring experience; or equivalent combination of education, training and experience.
  • At least 2-3 years leading clinical research studies (regional and/or globally speaking). Involvement in cross-functional, multicultural and international clinical trials; demonstrated capabilities in supporting operational aspects of clinical trial related activities.
  • Fluent English (oral and written).

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

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