Cra ii jobs in Australia

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · Performs site qualification, site initiation, interim monitoring, site management activities ...

The CRA II will perform site qualification, site initiation, interim monitoring, site management activities and close-out visits to ensure regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. The CRA II will also verify the process of obtai ...

Precision for Medicine is looking for an CRA II/ Senior CRA in Australia. The CRA II/ Senior CRA provides overall support to study sites and clinical project teams engaged in clinical research studies. · ...

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings ...

Clinical Research Associate II role at ICON plc, a world-leading healthcare intelligence and clinical research organization, involves designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments and therapies. · ...

Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Leads procedures and guidelines from different sponsors and/or monitoring environments. Acts as a site processes specialist, ensuring that the trial is conducted in ...

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · Leads procedures and guidelines from different sponsors and/or m ...

Precision for Medicine is looking for an CRA II/ Senior CRA in Australia. The CRA II/ Senior CRA provides overall support to study sites and clinical project teams engaged in clinical research studies. · ...

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · Leads procedures and guidelines from different sponsors and/or m ...

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. Leads procedures and guidelines from different sponsors and/or mon ...

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · Conduct remote monitoring of trial sites to verify compliance with regulatory requirements a ...

Join our team and take advantage of these great benefits Apply now to learn more about the full range of benefits we offer. · Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · Leads procedures and guidelines from ...

We are seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of in ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team, embedded within one of our largest, leading FSP partnership. · Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. · Ensuring protocol comp ...

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · Leads procedures and guidelines from different sponsors and/or m ...

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · Monitors investigator sites with a risk-based monitoring approac ...

As an experienced Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. · Perform all aspects of CRA duties from site selection, site initiation, through to site routine monito ...

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation. · Monitors investigator sites with a risk-based monitoring approac ...

Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to ...

We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. · Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate wit ...