Conduit

ACUTA

www.iqvia.com

Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.

Open roles
40
New role every
~0.1 days

Company signals

Score: 69
Wikipedia Yes Repost rate (90d) 2% Stale listings 0% GitHub org Yes Median listing lifespan 2 days Missing required salary 100% Wide pay-band rate 80% New cities (90d) 1

Job facts

Location
São Paulo, Brazil
Type
Full-time
Posted
Jun 09, 2026
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Site Enrollment and Engagement Lead - Colorectal Cancer - Brazil

at ACUTA


Job Overview

Site Enrollment and Engagement Lead - Brazil collaborate with research staff and key stakeholders to enhancetrial recruitment and support study‑specific training needs. Serves as a strategic partner to internal and external teams, optimizing site experience and performance. This role also leads relationship management and communication of medical and scientific information with healthcare providers and site staff .

Essential Functions

  • 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, screening, and enrollment.

  • Complete internal electronic reporting, organize group events, and manage objections effectively.

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

Qualifications

  • 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.

  • Study Coordinator, Clinical research coordinator , Clinical Trial Liason , CRA, preferred.

  • 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 asolutions‑based approach.

  • Positive, proactive mindset with strong customer service orientation.

  • Collaborative mentality and cultural awareness.

  • High flexibility for travel, up to 70% , strong team‑player aligned with IQVIA group values.

  • Willingness to mentor others and take on responsibilities beyond core role.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.