IQVIA

ClinicalTrialEducator

Mexico City, Mexico FULL TIME
The Brief

“Clinical Trial Educator at IQVIA. Skills: trial recruitment, study-specific training needs, relationship management, communication of medical and scientific information. Work with research sites to develop study‑specific action plans to accelerate patient recruitment or support procedural training. Provide practical support to study sites to maximize potential for patient enrolment”

What You'll Achieve.

enhance trial recruitment; support study‑specific training needs; optimizing site experience and performance; accelerate patient recruitment; support procedural training; maximize potential for patient enrolment; maximize pre‑screening, screening, and enrollment

Industry & Context.

Problems you'll solve

identify and address recruitment barriers; Ability to quickly understand situations and apply a solutions-based approach

Eligibility Requirements

High flexibility for travel, up to 70%

What They're Looking For.

Must Have

Bachelor’s degree in Health Sciences or related field, or equivalent professional qualifications, Intermediate/advanced level of English, Registered Nurse or other healthcare professional background required, Excellent interpersonal and communication skills, Ability to execute tasks with minimal oversight and make informed decisions independently, Strong coordination skills across multiple functions, Ability to quickly understand situations and apply a solutions-based approach, Positive, proactive mindset with customer service orientation, Collaborative mentality and cultural awareness, High flexibility for travel, up to 70%, Willingness to mentor others and take on responsibilities beyond core role

Nice to Have

Experience as a Study Coordinator, Clinical research coordinator, Clinical Trial Liason preferred 1-2 years, Location: Mexico City preferred

What You'll Do.

Work with research sites to develop study‑specific action plans to accelerate patient recruitment or support procedural training

Provide practical support to study sites to maximize potential for patient enrolment

Work with research sites to identify and address recruitment barriers – identify common site issues and work with the sponsor and relevant stakeholders to recommend creative options to overcome these barriers

Act as a resource for healthcare professionals at clinical study sites by sharing best practices and strategies for patient identification and retention

Conduct recruitment training sessions

Identify patient flow / pathway through site and work with identified departments to raise awareness of protocols and the potential for patient inclusion

Provide education to healthcare professionals and staff

reinforcing study protocols and trial requirements

Maintain and analyze customer records to tailor strategies that maximize pre‑screening

Complete internal electronic reporting

organize group events

and manage objections effectively

Keep up‑to‑date technical knowledge of the assigned specialty and disease areas

How You'll Work.

Team & Collaboration

collaborate with research staff and key stakeholders; serves as a strategic partner to internal and external teams; work with the sponsor and relevant stakeholders; team-player aligned with IQVIA and CTE group values

Communication Scope

Excellent interpersonal and communication skills; communication of medical and scientific information

Process & Methodology

develop study‑specific action plans, organize group events

Free ATS check

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