Jobs: clinical monitor

Company Description PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description PSI Medical Monitors provide medical input...

PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job DescriptionPSI Medical Monitors provide medical input to global clinical...

Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources + improve impact for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough...

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights...

Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we...

Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we...

Company DescriptionPSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job DescriptionPSI Medical Monitors provide medical input to...

Company DescriptionPSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job DescriptionPSI Medical Monitors provide medical input to...

Job DescriptionThe Clinical Research Associate (CRA) is accountable for the overall performance and compliance of assigned clinical trial sites and protocols within [country]. Under the oversight of the CRA Manager, you will ensure that study conduct at your sites is fully compliant with ICH/GCP, local regulations, and internal policies and procedures,...

Job DescriptionThe Clinical Research Associate (CRA) is accountable for the overall performance and compliance of assigned clinical trial sites and protocols within [country]. Under the oversight of the CRA Manager, you will ensure that study conduct at your sites is fully compliant with ICH/GCP, local regulations, and internal policies and procedures,...

Job DescriptionThe Clinical Research Associate (CRA) is accountable for the overall performance and compliance of assigned clinical trial sites and protocols within [country]. Under the oversight of the CRA Manager, you will ensure that study conduct at your sites is fully compliant with ICH/GCP, local regulations, and internal policies and procedures,...

Responsible for the clinical operations of a project within a defined regional/global level.  Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations.  The COL acts as a primary...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison...

A global CRO is looking to hire an experienced CRA to join them on a permanent basis. Working one day per week onsite in Bucharest, the successful candidate will play a critical role in overseeing and managing a sponsor's clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.Role...

Job DescriptionThe Clinical Research Associate (CRA) is accountable for the overall performance and compliance of assigned clinical trial sites and protocols within [country]. Under the oversight of the CRA Manager, you will ensure that study conduct at your sites is fully compliant with ICH/GCP, local regulations, and internal policies and procedures,...

Responsible for the clinical operations of a project within a defined regional/global level.  Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations.  The COL acts as a primary...

Responsible for the clinical operations of a project within a defined regional/global level.  Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations.  The COL acts as a primary...

Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered.Job OverviewClinical Trial Managers (CTM) are an integral part of clinical trial delivery, leading and working...

Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...

Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the...