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Job Description

Clinical Lead - Sponsor Dedicated

Mexiko-Stadt, Mexiko R1478856 HOME-BASED

Kolumbien| Argentinien| Remote| Mexiko

JETZT BEWERBEN

Stellenbeschreibung

Clinical Lead - Global Scope

Model:Sponsor Dedicated
Work Modality:Home Based
Hiring Countries:Mexico, Brazil, Argentina, Colombia

About the Role:
Clinical Leads are pivotal in clinical trial delivery, collaborating with clinical teams to accelerate the introduction of new drugs to the market, ultimately improving patients' lives.

As a Clinical Lead, you will be a key member of the core project team, ensuring the clinical delivery of studies in alignment with contractual requirements, Standard Operating Procedures (SOPs), policies, and practices.

Key Responsibilities:

  • Ensure clinical delivery of assigned projects in compliance with regulatory requirements (ICH-GCP, protocol), customer requirements (contract), and internal requirements (policies, SOPs, project plans).

  • Be accountable for meeting project recruitment targets and implementing effective recruitment strategies.

  • Contribute to the development of project risk mitigation plans and manage clinical risks throughout the project's lifecycle.

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

  • Identify the clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.

Qualifications:

  • Advanced degree or equivalent education in life sciences/healthcare recommended.

  • 7 years of clinical research/monitoring experience, or an equivalent combination of education, training, and experience.

  • At least 2 years of experience leading clinical research studies (regionally and/or globally), ideally with experience in Phase 1 and US region. Proven involvement in cross-functional, multicultural, and international clinical trials, with demonstrated capabilities in supporting operational aspects of clinical trial activities.

  • Fluent in English (oral and written).

  • Experience in Oncology, Onco-hematology, and/or GVHD is highly valued (not mandatory).

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

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