Clinical Research Associate I - II
Open to consider experienced CRAs based in Melbourne or Sydney. CRA experience from AUS or NZ is required (at least 1 year of independent monitoring)Key AccountabilitiesMaintenance (from initiation through close out):Act as Parexel's direct contact with a…
Clinical Operations Assistant (COA/ CTA)
This Clinical Operations Assistant (COA/ CTA) role will perform the role of COA to support inhouse tasks for the assigned trials, and will be provided CRA training and exposure depending on individual's progress and performance.Clinical Trials experience as SC…
Investigator Contracts Lead - FSP
Key Accountabilities:Contracting deliverablesExercise good judgment in balancing the risks to the client in making budget and contractual decisions against the impacts to client clinical trial timelinesFollow client processes to develop, negotiate, track and e…
Site Activation Specialist – Study Start-Up
A global clinical research organization is seeking a Clinical Trial Site Activation specialist in Australia. This role involves coordinating start-up activities, submitting regulatory documents, and ensuring compliance with clinical trial standards. The ideal …
Clinical Research Associate I - II
* Open to consider experienced CRAs based in Melbourne or Sydney.* CRA experience from AUS or NZ is required (at least 1 year of independent monitoring)Key Accountabilities:Maintenance (from initiation through close out):Act as Parexel’s direct contact with …
Site Activation Specialist – Study Start-Up
A global clinical research organization is seeking a Clinical Trial Site Activation specialist in Australia. This role involves coordinating start-up activities, submitting regulatory documents, and ensuring compliance with clinical trial standards. The ideal …
Site Activation Specialist – Study Start-Up
A global clinical research organization is seeking a Clinical Trial Site Activation specialist in Australia. This role involves coordinating start-up activities, submitting regulatory documents, and ensuring compliance with clinical trial standards. The ideal …
Site Activation Specialist – Study Start-Up
A global clinical research organization is seeking a Clinical Trial Site Activation specialist in Australia. This role involves coordinating start-up activities, submitting regulatory documents, and ensuring compliance with clinical trial standards. The ideal …
Site Activation Specialist – Study Start-Up
A global clinical research organization is seeking a Clinical Trial Site Activation specialist in Australia. This role involves coordinating start-up activities, submitting regulatory documents, and ensuring compliance with clinical trial standards. The ideal …
Site Activation Specialist – Study Start-Up
A global clinical research organization is seeking a Clinical Trial Site Activation specialist in Australia. This role involves coordinating start-up activities, submitting regulatory documents, and ensuring compliance with clinical trial standards. The ideal …