Iqvia

clinical research services, commercial insights, and healthcare intelligence

ClinicalTrialEducator

Madrid, Spain FULL TIME Remote Friendly
The Brief

“Clinical Trial Educator at Iqvia. Skills: trial recruitment, study-specific training needs, relationship management, communication of medical and scientific information. Works with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure training. Provides education to healthcare professionals and their staff, reinforcing study protocols as related to a clinical trial”

What You'll Achieve.

optimize the site experience and performance; accelerate recruitment; support study-specific procedure training; maximize pre-screening, screening, and enrollment in trials; optimize program delivery

Industry & Context.

clinical research services, commercial insights, and healthcare intelligence
Problems you'll solve

Solutions-based approach to problem-solving

Eligibility Requirements

High flexibility to travel (internationally, if needed), fixed-term opportunity for 12 months contract

What They're Looking For.

Must Have

Registered Nurse or CRA experience is required, 1–2 years of prior relevant experience, High flexibility to travel (internationally, if needed), Clinical competence in relevant therapeutic area, Excellent interpersonal and communication skills, written and verbal communication skills, including good command of English, Ability to execute tasks with minimal oversight, Ability to coordinate and complete activities across multiple functions, Solutions-based approach to problem-solving, Positive, can-do attitude, customer service orientation, Collaborative mindset and team player, Demonstrates empathy and awareness of cultural differences, Upholds the values of IQVIA and the CTE group

What You'll Do.

Works with research sites to develop study-specific action plans to accelerate recruitment or support study-specific procedure training

Provides education to healthcare professionals and their staff

reinforcing study protocols as related to a clinical trial

May partner with referral networks to identify potential subjects for a trial

Maintains and analyzes customer records to customize strategies to maximize pre-screening

and enrollment in trials

Completes internal electronic reporting organizes and holds group events to optimize program delivery

Successfully manages objections raised

Maintains up-to-date technical knowledge of specialty and disease areas

How You'll Work.

Team & Collaboration

collaborate with research staff and other stakeholders; acts as a strategic partner to both external and internal stakeholders; partner with referral networks; Ability to coordinate and complete activities across multiple functions; Collaborative mindset and team player

Communication Scope

Excellent interpersonal and communication skills; written and verbal communication skills, including good command of English; communication of medical and scientific information

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