Site Enrollment and Engagement Lead - Argentina

IQVIA; Buenos Aires; Sur place; ARS 92 241 000 - 138 361 000; Plein temps

Résumé du poste

IQVIA is seeking an Site Enrollment and Engagement Lead for Argentina to collaborate with research staff and stakeholders to enhance trial recruitment and training needs. You will partner with internal and external teams to optimize site experience and performance, and mentor others while traveling up to 70% to study sites.

You will lead communication of medical information to healthcare providers and site staff, conduct recruitment training, and analyze site records to tailor strategies for

Qualifications

• Bachelor’s degree in Health Sciences or related field or equivalent qualifications.
• English at intermediate/advanced level.
• RN or healthcare professional background is required.
• Experience as Study Coordinator, Clinical Research Coordinator, Clinical Trial Liaison or CRA is preferred.
• Strong interpersonal and communication skills with the ability to work independently.

Responsabilités

• Collaborate with research sites to develop study-specific action plans to accelerate recruitment.
• Provide practical support to sites to maximize patient enrolment potential.
• Identify recruitment barriers and propose creative options with sponsor and stakeholders.
• Act as a resource for healthcare professionals by sharing best practices for patient identification and retention.
• Conduct recruitment training sessions.
• Map patient flow at sites and raise protocol awareness across departments.
• Educate staff on study protocols and trial requirements.
• Maintain and analyze records to tailor pre-screening and enrollment strategies.
• Complete internal reporting, organize group events, and manage objections effectively.
• Stay updated on knowledge within assigned specialty and disease areas.

Connaissances

Interpersonal skills

Communication skills

Customer service orientation

Collaborative mindset

Problem solving

Travel readiness

Mentorship willingness

Team player

Formation

Bachelor’s degree in Health Sciences or related field

Registered Nurse or healthcare professional background

Study Coordinator/Clinical Research Coordinator/CRA experience

Description du poste

Job Overview

Site Enrollment and Engagement Lead - Argentina collaborate with research staff and key stakeholders to enhance trial 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 a solutions‑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.