Site Partner Ii / Senior Site Partner (ssu - Regulatory Submissions)
ICON
São Paulo, Brazil
Not specified; competitive base salary + performan...
Hybrid
Ethics submission experience cep/conep in cros
Site-facing position experience in study start up
Expert knowledge of ich/gcp and local regulations
ICON is a global healthcare intelligence organization seeking a Site Partner to independently manage relationships with investigator sites across studies
Job Summary
ICON is a global healthcare intelligence organization seeking a Site Partner to independently manage relationships with investigator sites across studies.
The role requires expert preparation of site documentation for regulatory submissions including CEP/CONEP and ensuring timely ethics approvals according to local requirements.
Candidates must possess a Bachelor's degree in life sciences or equivalent experience with mandatory ethics submission experience in CROs.
Matching Summary
ICON is a global healthcare intelligence organization seeking a Site Partner to independently manage relationships with investigator sites across studies.
Salary
Not specified; Competitive base salary and performance incentives mentioned; Comprehensive benefits package including health and retirement plans
Skills & Requirements
Must-have
Ethics submission experience CEP/CONEP in CROs
Site-facing position experience in Study Start Up
Expert knowledge of ICH/GCP and local regulations
Fluent English communication writing and reading
Experience with Patient Informed Consent adaptation
Nice-to-have
Proactive risk assessment and contingency planning
Collaborative team player with high-quality focus
Ability to manage multiple sites and competing priorities
Subject Matter Expertise in changing regulatory requirements
Key Requirements
Bachelor's degree in life sciences or related field
MUST HAVE ethics submissions experience CEP/CONEP in CROs
Experience in site-facing roles such as Study Start Up or Regulatory Associate
Legal right to work in Brazil (implied by location)