In-House Clinical Research Associate I

🔥 1 hour ago

🇦🇺 Australia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 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

Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Support site start-up activities, including feasibility questionnaire coordination, confidentiality agreement collection, and essential document management • Coordinate distribution and tracking of study materials to investigative sites and maintain accurate documentation • Review site documentation for quality and completeness • Support Trial Master File (TMF) maintenance and reconciliation activities • Conduct remote monitoring activities and support pre-study, initiation, interim, and closeout visits under the guidance of Clinical Trial Managers and field CRAs • Maintain regular communication with investigative sites and provide operational support • Help resolve study-related questions and issues • Review electronic case report forms and study data for completeness, consistency, and compliance • Assist sites with data management queries, vendor-related requests, study recruitment activities, and subject eligibility tracking • Generate study reports, maintain study trackers, and provide operational updates for project oversight and decision-making • Support site personnel changes, training documentation, regulatory document collection, and vendor access management • Collaborate with Clinical Trial Managers, field CRAs, sites, and cross-functional project teams to support clinical research studies and compliance with GCP, applicable regulations, and study requirements

🎯 Requirements

• A four-year degree with a concentration in medical, biological, physical, health, pharmacy, or another related science field preferred; alternatively, equivalent education, training, and relevant clinical research experience • Clinical research experience in roles such as Study Coordinator, Clinical Trial Assistant, or other relevant research positions • Understanding of clinical research principles, processes, and Good Clinical Practice (GCP) requirements • Knowledge of FDA and/or EU regulations, ICH Guidelines, local regulatory requirements, and standard operating procedures • Familiarity with electronic data capture (EDC), eCRF, IVRS, and other clinical research systems • Strong planning, organization, and time management skills with the ability to manage multiple priorities effectively • Excellent communication and interpersonal skills with the ability to collaborate across sites and cross-functional teams • Proficiency in spoken and written English • Candidates must be based in Australia

🏖️ Benefits

• Diverse and inclusive work environment • Supportive and cohesive teams • Accessible leadership • Equal employment opportunities • Exceptional employee experiences • Remote work arrangement