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Study Start Up Associate I

ICON · Buenos Aires, Argentina

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Clinical OperationsFull-timeCompany career page

RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.

Role summary

Study Start Up Associate I will facilitate clinical trial initiation at ICON Strategic Solutions in Buenos Aires, ensuring regulatory compliance and coordinating approvals across internal and external stakeholders to support innovative treatment development.

What they're looking for

  • Bachelor's degree in life sciences or related field
  • Study start-up or site activation experience in Argentina
  • 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 necessary approvals for study initiation
  • Maintain accurate records of regulatory submissions and approvals
  • Support study teams in developing protocols, informed consent forms, and investigator brochures
  • Participate in study start-up meetings and advise on regulatory requirements and timelines

Privacy & handoff

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What RoleLantern checked

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RoleLantern checkedNeeds clarity
Date posted7 days ago
Last source checkToday
Salary listedNeeds clarity
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