Clinical Research Associate II

🔥 44 minutes ago

🇦🇺 Australia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• Manage the clinical aspects of full-service global projects in Australia • Conduct and report all types of onsite monitoring visits • Participate in study startup • Perform CRF review, source document verification, and query resolution • Facilitate site budgets and contract negotiations • Monitor trial progress at the country level • Manage site communication • Serve as a point of contact for in-house support services and vendors • Communicate with internal project teams regarding study progress • Participate in feasibility research • Support the regulatory team in preparing documents for study submissions • Build and maintain relationships with clinical sites and investigators • Ensure timelines, targets, and clinical research standards • Focus on subjects’ rights, safety, well-being, and data quality compliance

🎯 Requirements

• College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience • At least 2 years of independent on-site monitoring experience in Australia • Experience in all types of monitoring visits in Phase II and/or III • Experience in Inflammatory Bowel Disease, Oncology, or Infectious Diseases is a plus • Full working proficiency in English • PC skills to be able to work with MS Word, Excel and PowerPoint • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel

🏖️ Benefits

• Competitive salary • Hybrid work arrangement: 2 days flexi and 3 days in office • Onsite Gym access • Additional 5 days of wellness leave • Development and learning opportunities • Chance to make a real impact in a meaningful industry • Continuous support from global peers • On-the-job learning experiences • Formal development programs • Career growth opportunities