Study Delivery Specialist

Posted 58mins ago

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Job Description

Study Delivery Specialist supporting clinical trial site monitoring for ICON’s global healthcare research organization. Assisting with compliance, documentation, data entry, and site performance tracking.

Responsibilities:

  • Assist in monitoring clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines
  • Support site management activities, including documentation preparation, data entry, and tracking site performance metrics
  • Collaborate with cross-functional teams to facilitate communication and address site-related issues
  • Maintain accurate records of site activities and contribute to preparing monitoring reports
  • Participate in training and development initiatives to enhance knowledge and skills in clinical trial management

Requirements:

  • Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research
  • Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory
  • Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively
  • Basic knowledge of clinical trial processes and regulatory requirements is a plus
  • Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment
  • Legal right to work in the country where the role is based

Benefits:

  • 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 wellbeing resources
  • Learning and development opportunities through structured training and career pathways