Parexel Jobs in Australia

This Clinical Operations Assistant role will support inhouse tasks for assigned trials and provide CRA training. Clinical Trials experience is desirable. · The role requires working from Sydney office some days and remotely the rest. · ...

Support feasibility processes for clinical trials by conducting research and data analysis to identify potential Clinical Trial Investigators and sites. · ...

This role involves supporting in-house tasks for assigned trials as a Clinical Operations Assistant. · Key Responsibilities: · Assist site staff access to vendor systems · Maintain Trial Master File quality: upload documents; update EDL; resolve quality issues · Support investiga ...

At Parexel we all share the same goal - to improve the world's health. · ...

Job Description · Clinical Research Associates (CRAs) work closely with investigators and site staff to ensure the integrity of study implementation. · Maintenance from initiation through close out: · Act as Parexel's direct contact with assigned sites, assess and ensure overall ...

Job Description · The Regulatory Affairs Consultant will be responsible for supporting Global Labeling, Regulatory (Clinical / Safety), or Medical Writing for labelling updates. · Use of document management tools (internal systems) and external platforms. · ...

The Feasibility Specialist is responsible for supporting feasibility processes for clinical trials. · Supporting the Feasibility, Strategy, & Analytics Lead (FSAL) to ensure knowledge of the goals, scope and requirements of a Site Feasibility project, · Clinical Systems Support: ...

We're looking for a Clinical Research Associate I to join our team at Parexel in Australia. · ...

At Parexel, we all share the same goal - to improve the world's health. · ...

This is a Regulatory Affairs Consultant role that requires previous experience working in industry in support of Global Labeling, Regulatory (Clinical / Safety), or Medical Writing for labelling updates. The candidate should have strong familiarity with the Company Core Datasheet ...

The Feasibility Specialist is responsible for supporting feasibility processes for clinical trials. · ...

Assist inhouse tasks for assigned trials and provide CRA training and exposure. · To support project initiation & planning by assisting with site activation, data management and quality assurance. · ...

A clinical research organization seeks a Clinical Operations Assistant in Sydney. Responsibilities include maintaining Trial Master File quality and assisting site staff with vendor systems. · Key Responsibilities: · Maintain high-quality Trial Master Files · Assist site staff wi ...

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. · ...

We all share the same goal - to improve the world's health. · Minimum of a Bachelor's Degree in a Scientific or Technical Discipline · ...

Clinical Research Associate I Job Description · At Parexel, we value collaboration and teamwork to deliver exceptional results. · Maintenance: · Act as Parexel's direct contact with assigned sites, · ...

This Clinical Operations Assistant (COA/ CTA) role will perform the role of COA to support inhouse tasks for the assigned trials. · Contribute to site activation by: Assisting with the site staff access to vendor systems · Access reconciliation quarterly · Following-up with sites ...

The Feasibility Specialist is responsible for supporting feasibility processes for clinical trials. This role involves conducting research and data analysis to identify potential Clinical Trial Investigators and sites. · ...

Job Description: · Solid experience in global CMC regulatory from local/global pharma relevant · Expertise in global CMC requirements post-marketing variations biologicals vaccines preferred EU US FDA · We seek senior regulatory affairs expert develop strategies manage submission ...

Job summaryClinical Research Associate I performs site management and monitoring tasks for clinical trials. · ...