PSI CRO Jobs in Israel

Join our team of experts in regulatory and ethics submissions of clinical studies. · ...

Take your career to the next level and lead challenging study activation process on a country level. · ...

The position is for a Country Approval Specialist who will focus on facilitating the start of research projects of novel medicinal products. · ...

Join our international team and be the key support to clinical research projects. · ...

Lead challenging study activation process on a country level and support clinical research teams. · Finalize site/vendor agreements and negotiate budgets for smooth study start-ups. · ...

We are looking for a Country Approval Specialist to join our team of experts in regulatory and ethics submissions of clinical studies. · ...

Take your career to the next level and lead challenging study activation process on a country level. · ...

Take your career to the next level and lead challenging study activation process on a country level. · ...

As a Clinical Research Associate at PSI, you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications. · ...

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. · ...

+Clinical Research Associate II en PSI: realizar tareas de monitoreo clínico y trabajar en estudios clínicos en diferentes indicaciones terapéuticas. · + · , · , · ...

We are looking for a knowledgeable, proactive and dedicated person to support and develop our Clinical Operations team in Israel. The scope of responsibilities will include management of multiple aspects of clinical research from business development to project execution. · ...

Join our international team and be the key support to clinical research projects. · ...

Take your career to the next level and lead challenging study activation process on a country level. · ...

Job summary · Join our team of experts in regulatory and ethics submissions of clinical studies. · ...

Clinical research associate to perform monitoring tasks and work on clinical studies in different therapeutic indications at PSI Contract Research Organization. · ...

+You will facilitate the start of research projects of novel medicinal products while taking a step further in your professional career. · ++Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities. · Communicate with regulatory authorities, ethics committ ...

+h2>Job summary · Enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications. · +College/University degree in Life Sciences or an equivalent combination of education, training & experienceFull working proficiency in Hebrew and English · ...

We focus on delivering quality and on-time services across a variety of therapeutic indications. · College/University degree in Life Sciences or an equivalent combination of education, training & experience · ...

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. · ...