Site Partner

ICON

Moema, São Paulo, Brazil
Not specified; competitive salary mentioned; range...
Hybrid
Ethics submission experience cep/conep in cros
Site-facing position experience in start-up or activation
Expert knowledge of icon sops and ich/gcp guidelines
ICON is seeking a Site Partner for their São Paulo office, responsible for managing relationships with investigator sites to support their engagement and performance in clinical studies. The ideal candidate should have experience in ethics submissions and site-facing roles within CROs or healthcare, along with a bachelor's degree in a related field

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Site Partner to independently manage investigator site relationships.
  • The role requires expert-level independent coordination of all activities necessary to achieve timely site activations while ensuring accurate documentation for regulatory submissions.
  • Candidates will act as a trusted liaison advocating for site needs internally while driving project outcomes through proactive risk assessment and issue resolution.

Matching Summary

Match Score: 85

ICON is seeking a Site Partner for their São Paulo office, responsible for managing relationships with investigator sites to support their engagement and performance in clinical studies. The ideal candidate should have experience in ethics submissions and site-facing roles within CROs or healthcare, along with a bachelor's degree in a related field.

Salary

Not specified; Competitive salary mentioned; Range of additional benefits including health insurance and retirement planning

Skills & Requirements

Must-have

  • Ethics submission experience CEP/CONEP in CROs
  • Site-facing position experience in start-up or activation
  • Expert knowledge of ICON SOPs and ICH/GCP guidelines
  • Fluent English communication writing and reading skills
  • Proactive coordination of site activation and maintenance tasks

Nice-to-have

  • Experience in site selection and qualification tasks
  • Ability to manage multiple sites and competing priorities
  • Collaborative team player committed to high-quality site experience
  • Strong understanding of factors influencing recruitment and quality

Key Requirements

  • Bachelor's degree in life sciences, healthcare, business, or related field
  • MUST HAVE ethics submissions experience CEP/CONEP in CROs
  • MUST HAVE experience in site-facing positions such as Study Start Up or Regulatory Associate

Work Rights

Not specified

Tailored Resume

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