Clinical Research Site Specialist

One Clinical Research (OCR)OCR is a leader in conducting cancer clinical trials, specialising in pharmaceutical industry-sponsored clinical trials for patients with haematological (blood) or solid-organ cancers.The successful candidate will be primarily responsible for the review and oversight of clinical trials conducted at OCR, with a strong focus on...

Various Clinical Trial Coordinator/Assistant Roles AvailableImmediate Start Available - Nedlands, Western AustraliaExciting opportunities for experienced Clinical Research Professionals to join a dynamic and growing team. Positions available include:Senior CTC/Project LeadCTC (Clinical Trial Coordinator)CTA (Clinical Trial Assistant)Full time positions...

Job Overview:Our organization is seeking a highly skilled individual to fill the role of Clinical Research Site Specialist. This position plays a critical role in the start-up and activation of clinical research sites, supporting processes to optimize country & site selection activities. Key ResponsibilitiesSite Activation: Deploy global site strategies by...

About usHere at Linear, we are a not-for-profit organisation that supports medical research by delivering world-class clinical trials across a wide range of therapeutic areas. Our medical, clinical and project teams work collaboratively across our clinical trial centres in Joondalup and Nedlands and are now looking for a Clinical Trial Administrator to join...

Research Perth Part Time Research at Icon Group Join an innovative company that provides exceptional personalised cancer care services.Collaborate to coordinate and conduct clinical trials.Gain exposure and access to our cutting-edge services at our new Icon Cancer Centre site in Hollywood.The Hollywood facility, which is delivered in partnership with Perth...

Job SummaryWe are seeking a highly skilled Site Care Associate to join our team. The ideal candidate will play a critical role in the start-up and activation of clinical research sites, supporting processes to optimize country & site selection activities.Key ResponsibilitiesSite Activation: Deploy global site strategies by qualifying and activating assigned...

Job OverviewWe are seeking an experienced professional to perform site qualification, site initiation, interim monitoring, site management activities and close-out visits ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) compliance.The ideal candidate will have a strong understanding of clinical trial protocols and be able to...

Key Responsibilities of a Clinical Research Associate">The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and reported data are accurate, complete, and verifiable from source documents.">Responsibilities include:Building relationships with Principal Investigators, study...

OverviewJoin to apply for the Clinical Research Associate (WA) role at Novotech.The Clinical Research Associate (CRAII - CRAIII) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between...

OverviewJoin to apply for the Clinical Research Associate (WA) role at Novotech.The Clinical Research Associate (CRAII - CRAIII) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between...