Clinical Study Manager

**Quality Assurance Manager - location flexible****Who are we?**We're Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980's. If you already work in this industry you'll...

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**Full time, permanent, office based position at our Head Office in Firle, South Australia.****Who are we?**We're Avance Clinical a Contract Research Organisation. We offer specialised services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980's....

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Job OverviewThis is a key role within our clinical research organisation, with Senior Clinical Research Associates working closely with client study teams and supported by a dedicated ICON line manager.Key Responsibilities:Manage all aspects of CRA duties from site selection to close-out visits and database lock.Ensure high-quality data and consistently low...

**This is a rare opportunity to join our high performing QA team. If you are currently working for a CRO or Pharma organisation in GCP Quality Assurance, then we'd love to hear from you.*****Adelaide - office based*****Who are we?**We're Avance Clinical an Australian based Contract Research Organisation. We offer specialised services supporting drug...

Key Responsibilities:Oversee the management of clinical trials from initiation to completion in adherence to ICH-GCP and local regulations.Ensure effective risk management for assigned studies within Australia.Collaborate with internal and external stakeholders to ensure timely and cost-effective execution of clinical trial deliverables.Lead a regional team...

Overview Of RoleResponsible for the management and oversight of phase I-IV clinical trials from start up through CSR, including development of project documentation, training project staff, monitoring study progress, assessing protocol adherence, administration and oversight of study budgets, monitoring site-level activities, and management of third-party...

Job OverviewThis role entails overseeing clinical studies from initiation to completion, ensuring adherence to regulatory requirements and industry standards.Site Management: Identify, launch, and monitor study sites to guarantee high-quality data on time and within budget.Study Training: Provide ongoing education to site staff on ICH-GCP, GCP, and study...

Job Role OverviewWe are seeking a highly skilled professional to lead our clinical research initiatives as a Senior Clinical Research Associate.This role involves developing and maintaining strong relationships with clinical sites, ensuring seamless site interactions throughout the trial lifecycle.The ideal candidate will be responsible for conducting...