Clinical Trial Educator - Alzheimer's Disease

IQVIA; Ciudad de México; Presencial; MXN 551,000 - 735,000; Jornada completa

Descripción de la vacante

A leading global clinical research organization is seeking a Clinical Trial Educator in Mexico City. This role involves collaborating with research sites to enhance patient recruitment and support clinical trial processes. Ideal candidates will hold a relevant Bachelor's Degree, have 1-2 years of experience, and possess strong communication skills. Flexibility to travel significantly is required.

Formación

• 1 - 2 years relevant experience as Study Coordinator or Sub-Investigator.
• Fluent English (written, spoken and read).
• Ability to travel 70% or more of the time.

Responsabilidades

• Develop study-specific action plans to accelerate patient recruitment.
• Provide education to health care professionals about clinical trials.
• Create and analyze strategies for patient screening and enrollment.

Conocimientos

Clinical trial management

Interpersonal communication

Problem-solving

Customer service

Educación

Bachelor's Degree in Health Sciences or Scientific

Descripción del empleo

Job Overview

CTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. Leads the relationship management and communication of medical and scientific information with health-care providers, patients, care givers.

Essential Functions

• Works with research sites to develop study-specific action plans to accelerate patient recruitment or support study-specific procedure training
• Provides education to health care professionals and their staff, reinforces study protocols as related to a clinical trial
• May partner with referral networks to identify potential subjects for a trial
• Creates and analyzes strategies to maximize patient pre-screening, screening, enrollment in trial
• Maintains up-to-date technical knowledge of specialty and disease areas

Qualifications

• Bachelor's Degree in Health Sciences (Nursing, Medicine, Pharmacist) or Scientific (Biochemical, Pharmaceutical Chemist).
• Typically requires 1 - 2 years of prior relevant experience as Study Coordinator or Sub-Investigator working with sites.
• Preferred experience in Alzheimer’s disease or Psychiatric disease.
• High flexibility to travel 70% or more of the time.
• Fluent English (written, spoken and read)
• Excellent interpersonal and communication skills
• Ability to execute tasks with minimal oversight
• Ability to coordinate and complete activities across multiple functions
• Ability to quickly gain an understanding of a situation and to have a solutions based approach to resolving problems
• Strong customer service approach
• Collaborative mentality

We are 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.

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