Study Start Up Associate I

ICON · Sao Paulo, Brazil

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Clinical OperationsFull-timeCompany career page

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Role summary

ICON seeks a Site Activation Partner to facilitate clinical trial initiation in São Paulo, Brazil. The role involves regulatory document preparation, stakeholder coordination, and study start-up support to advance innovative treatments.

What they're looking for

Bachelor's degree in life sciences or related field
Study start-up or site activation experience in Brazil
Strong attention to detail and organizational skills
Excellent communication and interpersonal abilities
Ability to manage multiple tasks independently in fast-paced environment
Clinical research or regulatory affairs experience preferred

What you'll be doing

Prepare and submit regulatory documents including clinical trial applications and ethics committee submissions
Coordinate with internal and external stakeholders to obtain study initiation approvals
Maintain accurate records of regulatory submissions and approvals
Support development of study documents such as protocols and informed consent forms
Participate in start-up meetings and advise on regulatory requirements and timelines

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Date posted10 days ago

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