Clinical Trial Coordinator at ICON plc | AU | Rezi

Clinical Trial Coordinator at ICON plc

Clinical Trial Coordinator

ICON plc · AU

3 weeks ago

Clinical Trial Coordinator

ICON plc · AU

22 days ago
Resume preview

Impress employers and recruiters.
Choose from hundreds of resume examples.

Target Resume Now
Resume preview

Tailor your resume to this Clinical Trial Coordinator role.

Rezi rewrites your resume against ICON plc's job description. Free.

Resume score gauge reading 58 out of 100

Don't guess if your resume is good enough.

See how it scores against the Clinical Trial Coordinator posting at ICON plc — free, in seconds.

About the Role

As a SMA I at ICON, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.

Responsibilities

  • Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
  • Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
  • Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
  • Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
  • Participating 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.
  • Willingness to travel as required (approximately 25%).
  • Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Skills

  • Organizational skills
  • Attention to detail
  • Communication skills
  • Interpersonal skills

Experience Level

  • Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.

Education Level

  • Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.

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

About the Company

  • ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
  • As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Equal Opportunity

  • ICON is an equal opportunity employer.
  • We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
  • If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.