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