Respiratory Trial Enrollment Lead: Site Engagement

IQVIA

Santiago

On-site

CLP 51,081,000 - 88,409,000

Full time

10 days ago

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Job summary

IQVIA is seeking a Site Enrollment and Engagement Lead to partner with research sites and study teams in Santiago. You will accelerate patient recruitment, support site training, and coordinate stakeholders to optimize enrollment and site performance.

The role requires collaboration across functions, excellent communication with healthcare providers, and willingness to travel up to 75% to support trial activities.

Qualifications

  • Bachelor’s degree in Health Sciences or related field.
  • Advanced level of English.
  • Experience as a Study Coordinator or Clinical Trial Liaison preferred 1–2 years.
  • Location to hire: Santiago, Chile.

Responsibilities

  • Develop study-specific action plans with research sites to accelerate patient recruitment.
  • Provide practical support to study sites to maximize enrollment potential.
  • Identify recruitment barriers and propose creative options with sponsors and stakeholders.
  • Share best practices with healthcare professionals at clinical study sites.
  • Conduct recruitment training sessions for study staff and site teams.
  • Maintain and analyze records to tailor strategies for pre-screening and enrollment.
  • Complete internal reporting, organize group events, and manage objections effectively.
  • Keep up-to-date technical knowledge of the assigned specialty and disease areas.

Skills

Advanced English
Interpersonal skills
Cross-functional coordination
Customer service orientation
Solution-oriented mindset

Education

Bachelor’s degree in Health Sciences or related field

Job description

IQVIA is seeking a Site Enrollment and Engagement Lead to partner with research sites and study teams in Santiago. You will accelerate patient recruitment, support site training, and coordinate stakeholders to optimize enrollment and site performance.

The role requires collaboration across functions, excellent communication with healthcare providers, and willingness to travel up to 75% to support trial activities.

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