Precision Medicine Group logo

Clinical Research Associate II

Job Overview

Location

Remote, Australia

Job Type

Full-time

Category

Product Management

Date Posted

April 14, 2026

Full Job Description

đź“‹ Description

  • • The Clinical Research Associate II (CRA II) provides essential support to study sites and clinical project teams engaged in clinical research studies, ensuring adherence to protocols, SOPs, and regulatory requirements such as ICH-GCP and local guidelines. This role is critical to maintaining patient safety, data quality, and study integrity across multiple clinical trials, particularly in Oncology and Rare Disease areas.
  • • Day-to-day responsibilities include overseeing study site management, conducting site visits (pre-study, initiation, routine monitoring, and close-out), verifying informed consent processes, reviewing investigator site files, managing investigational product inventory, identifying and reporting Serious Adverse Events, preparing monitoring reports, and supporting audit readiness. The CRA II also assists with site startup activities, budget negotiations, and contract execution under guidance, while maintaining strong relationships with investigators and study staff.
  • • Precision Medicine Group is a specialized CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to accelerate the development of life-changing therapies. The company focuses on Oncology and Rare Disease, offering a mission-driven environment where employees contribute to groundbreaking cancer therapies and are valued for their input and innovation.
  • • In this role, the CRA II will develop expertise in clinical monitoring, regulatory compliance, and cross-functional collaboration within global clinical trials. The position offers opportunities to strengthen skills in data review, risk management, stakeholder communication, and independent decision-making, while contributing to high-quality trial execution and professional growth within a supportive, innovative organization.

🎯 Requirements

  • • Bachelor’s degree or international equivalent in a business, scientific, or healthcare discipline (or equivalent combination of education and experience)
  • • Minimum of 2 years of on-site monitoring experience, with 1 year of oncology and Phase I experience preferred
  • • Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint) and fluency in English communication, both verbal and written
  • • Strong attention to detail, ability to work independently, and demonstrated customer service demeanor with flexibility and teamwork
  • • Working knowledge of the drug development process and willingness to travel 60-70% as required by project needs

🏖️ Benefits

  • • Opportunity to work on impactful clinical trials in Oncology and Rare Disease, contributing to life-changing therapies
  • • Support for professional growth through input being valued and nurtured, with ability to drive positive change within the organization
  • • Remote work flexibility with travel as required by project needs, enabling a balanced work arrangement
  • • Equal Opportunity Employer commitment, ensuring fair and inclusive hiring practices regardless of protected characteristics
  • • Access to company resources and support for reasonable accommodations during the application process for individuals with disabilities

Skills & Technologies

GCP
Junior
Remote
Degree Required

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Precision Medicine Group
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About Precision Medicine Group

Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.

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