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Site Specialist II - Clinical Research

icon · Lima

New
Hybrid Mid 🇬🇧 English
ICH-GCP Clinical trial management tools

Job description

About the role

ICON is a global healthcare intelligence and clinical research organisation. As a Site Specialist II, you will independently manage a range of site support activities and act as a key operational contact for sites, helping with efficient study start-up and maintenance. You will take responsibility for site management and operations deliverables, ensuring quality and efficiency.

Key responsibilities

  • Coordinate site-level document collection, review and maintenance, ensuring accuracy and compliance for assigned sites or studies.
  • Act as an operational liaison for site staff on documentation, systems and process questions.
  • Maintain up-to-date site status, metrics and key milestones in clinical trial management tools.
  • Support planning and logistics for site meetings, investigator meetings and monitoring visits.
  • Identify opportunities to streamline site workflows and contribute to process improvement.
  • Lead the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions and regulatory agency communications.
  • Liaise with internal and external stakeholders to obtain approvals and authorisations for study initiation.
  • Maintain accurate records of regulatory submissions, approvals and correspondence.
  • Guide study teams on regulatory requirements and best practices for study start-up.

Required profile

  • Bachelor's degree in life sciences, healthcare or a related field.
  • Clinical research experience, with at least 2 years in clinical research or regulatory affairs.
  • Specific experience in study start-up, including local and/or international regulatory processes and submissions to regulatory authorities and ethics committees.
  • Legal right to work in the country where the role is based.

Required skills

  • Strong understanding of regulatory requirements and guidelines, including ICH-GCP and local regulations.
  • Organizational and project management skills, able to handle multiple tasks and work with cross-functional teams.
  • Excellent communication skills in English and Spanish.

What we offer

  • Competitive base salary and performance-related incentives.
  • Health and wellbeing programmes, including medical, dental and vision coverage where applicable.
  • Retirement and pension plans, life assurance and disability coverage.
  • Employee assistance programmes and learning and development opportunities.

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Source : ats:workday

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Published 4 hours ago

Expires 1 month from now

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