Cra

This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the CRD or Head of Site Management and Monitoring, the person is accountable to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP.As line manager the role is critical...

:Title:CRADuration:12 monthsHours:average around 30 hours per weekLocation:Milan ItalyStarting salary:Good to have's:CTMSand Oracle Clinical experience is beneficial however it is a good to haveNice to haves:experience in working in teams, relationship builder, good knowledge of English, experienced in Italian language not less then 3 years of...

Company DescriptionOur client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA home based in Rome.Job Overview Monitoring clinical studies in phases II-III Assuring...

Linical Co., Ltd. ('Linical') is a premier global CRO headquartered in Osaka, Japan, listed in the prime segment of the Tokyo Stock exchange, and dedicated to serve its clients as a true partner in development. With more than 700 employees Linical directly covers a total of more than 20 countries in Europe, North America and Asia-Pacific including Japan via...

ConfidenzialeHealthcare ricerca per struttura sanitaria un/una OPERATORE SOCIO SANITARIO - OSS L'OPERATORE SOCIO SANITARIO opererà nella CRA di Confidenzialeolo d'Enza. La risorsa ideale possiede i seguenti:- Attestato di Oss - iscrizione al corso di Operatore Socio Sanitario;- Esperienza pregressa nel settore sanitario anche come ADB, OSA - OTA....

With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities...

Job Description:With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site...

The Clinical Research Associate RoleThe role of Clinical Research Associate involves overseeing the performance and compliance of assigned protocols and sites in a country. Under the guidance of the CRA manager, the individual ensures study conduct compliance with ICH/GCP, country regulations, Company policies, quality standards, and adverse event reporting...

The Clinical Research Associate RoleThe role of Clinical Research Associate involves overseeing the performance and compliance of assigned protocols and sites in a country. Under the guidance of the CRA manager, the individual ensures study conduct compliance with ICH/GCP, country regulations, Company policies, quality standards, and adverse event reporting...

The Clinical Research Associate RoleThe role of Clinical Research Associate involves overseeing the performance and compliance of assigned protocols and sites in a country. Under the guidance of the CRA manager, the individual ensures study conduct compliance with ICH/GCP, country regulations, Company policies, quality standards, and adverse event reporting...

The role of Associate Clinical Research Associate support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our...

Job Description:The role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally...

Job DescriptionWith support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site...

Job Description:The role is accountable for performance and compliance for assigned protocols and sites in acountry.Under the oversight of the CRA manager the person ensures compliance of study conduct withICH/GCP and country regulations, policies and procedures, quality standards andadverse event reporting requirements internally and externally.Acts as...

We are seeking a Study Start Up Specialist to be responsible for country study start up (SSU) activities and performing quality review of essential documents. The SSU Specialist is responsible for overseeing and leading SSU activities in collaboration with country team members (CLM and CRA) with the objective to improve site activation and maximize patient...

Job DescriptionWe aim to establish ourselves as the leading research-focused pharmaceutical company globally. Our dedication to improving healthcare accessibility is evident through our extensive policies, programs, and partnerships. At the forefront of combating diseases that affect both humans and animals, including cancer, HIV, Ebola, and emerging animal...

Job DescriptionWe are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a...

Job DescriptionWe are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we "follow the science" that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a...

The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, UK, US, Belgium, Czech Republic, Switzerland, Denmark, Romania, and India.The CRO occupies a unique position in the clinical...

The Italian affiliate of Novo Nordisk, based in Rome, is hiring a Clinical Research Manager (CRA Team Manager).Do you want to join one of the leading companies of the pharma sector? Do you want to build your career and contribute to the growth and development of the company? We're on the lookout for a knowledgeable, proactive, dedicated people manager to...