Logo of Huzzle

CRA II

image

ICON plc

3mo ago

  • Job
    Full-time
    Junior Level
  • Research & Development
    Healthcare
  • Sydney, +3
    Remote
  • Quick Apply

AI generated summary

  • You need a Bachelor's in a scientific or healthcare field, 2+ years as a CRA, knowledge of clinical trial processes and regulations, strong organizational skills, and ability to work independently.
  • You will conduct site visits, ensure protocol compliance, maintain data integrity, collaborate with site staff, resolve data queries, and assist in preparing study documentation.

Requirements

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.

Responsibilities

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

FAQs

What is the job title of this position?

The job title is Clinical Research Associate II (CRA II).

Where is this position based?

This position is home-based in Sydney, Melbourne, Brisbane, or Adelaide.

What type of organization is ICON plc?

ICON plc is a world-leading healthcare intelligence and clinical research organization.

What are the primary responsibilities of a CRA II?

Primary responsibilities include conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, and patient safety throughout the trial process, collaborating with investigators and site staff, performing data review, and contributing to study documentation preparation.

What qualifications are required for this position?

A Bachelor's degree in a scientific or healthcare-related field and a minimum of 2 years of experience as a Clinical Research Associate are required.

What knowledge is essential for this role?

In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines is essential for this role.

What skills are important for a CRA II?

Strong organizational and communication skills, attention to detail, and the ability to work independently and collaboratively in a fast-paced environment are important.

What benefits does ICON provide to its employees?

ICON offers a competitive salary, various annual leave entitlements, health insurance options, retirement planning, a global Employee Assistance Programme, life assurance, and flexible optional benefits.

Is there room for diversity and inclusion at ICON?

Yes, ICON values diversity, inclusion, and belonging and is committed to providing an inclusive and accessible environment for all candidates.

What if I have a medical condition or disability?

If you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position due to a medical condition or disability, please let us know.

Can I apply if I do not meet all the requirements?

Yes, you are encouraged to apply regardless of whether you meet all the requirements, as there’s a chance you may be exactly what ICON is looking for.

Science & Healthcare
Industry
10,001+
Employees

Mission & Purpose

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.