Offerte di lavoro per Clinical Trials Associate

Ora disponibile 47 i risultati sono coerenti

Ordina per:pertinenza - Data

CLINICAL TRIAL ASSISTANT  

Clinical Trial Assistant at ClinChoice (View all jobs) Parma, Italy Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring?...

AziendaGuarda Altre Offerte
IndirizzoParma, Emilia-Romagna
CategoriaScientifico
Data di pubblicazione 2 mesi fa Vedi dettaglio

Clinical Trial Assistant  

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Parma, Emilia-Romagna

Clinical Trial Assistant at ClinChoice (View all jobs) Parma, Italy Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring?...

Principal Clinical Trial Manager - Oncology or Ophtalmology experience required

Syneos Health

Italy-Europe - ITA-Home-Based, Italy

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committ...

Clinical Trial Assistant  

Guarda Altre Offerte

Parma, Emilia-Romagna

Clinical Trial Assistant at ClinChoice (View all jobs) Parma, Italy Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring?...

Clinical Associate  

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Turin, Piedmont, it

Clinical Project Associate - Milan office based What will you be doing? Maintains study documents and utilizes company systems to manage the bioanalytical data in support of clinical/pre-clinical studies. […]Works with the project...

Clinical Trial Assistant  

Guarda Altre Offerte

Parma, Emilia-Romagna

Clinical Trial Assistant at ClinChoice (View all jobs) Parma, Italy Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring?...

Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA  

Iqvia

Milan, Lombardy, it

Prepares and/or reviews regulatory documents to support clinical trial submissions.Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on c...

Clinical Research Associate (CRA)

Novartis

Force, Marche

-Planning, execution, and interpretation of clinical trials research, data collection activities and clinical operations. May interact with investigational sites, clinical consultants, Contract Research Organizations and other ven...

Clinical Research Associate II  

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Bologna, Emilia-Romagna

They offer a comprehensive range of pre-clinical and clinical development services, leveraging their expertise and proven methods to bring innovative ophthalmic solutions to market.They value a diverse and inclusive workplace wher...

Clinical Research Associate II  

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Bari, Puglia

They offer a comprehensive range of pre-clinical and clinical development services, leveraging their expertise and proven methods to bring innovative ophthalmic solutions to market.They value a diverse and inclusive workplace wher...

Trial Capabilities Associate (계약직 2)

Eli Lilly And Company

Location SEOUL, Seoul, Korea, Republic of

Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact for a site’s ERB and Competent Authorit...

Clinical Research Associate (Travel 30-50%)

Danaher

Location Solna, Sweden

Identify potential investigators, prepare site budgets and contract agreements  . Collect, review and process regulatory documents and correspondence from participating trial sites  . Review on-site files, product accountability l...

Clinical Research Associate, Site Management - Italy  

Iqvia

Milan, Lombardy, it

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice,...

Experienced Clinical Research Associate, Site Management - Italy  

Iqvia

Milan, Lombardy, it

Job OverviewPerform monitoring and Site Management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements...

CRA II / Senior Clinical Research Associate - Multisponsor  

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Palermo, Sicilia

Conduct, drive and manage country specific feasibility and/or site pre-qualification and qualification activities, which may include: -Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Cl...

Clinical Research Associate  

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Lazio

Monitor site compliance with study protocol and GCP. Perform source data review and verify adequacy of clinical data through comparison of case report forms to source documents per CMP. Ensure the site is entering data according t...

Clinical Research Associate  

Guarda Altre Offerte

Lazio

Monitor site compliance with study protocol and GCP. Perform source data review and verify adequacy of clinical data through comparison of case report forms to source documents per CMP. Ensure the site is entering data according t...

CRA II / Senior Clinical Research Associate - Multisponsor  

Guarda Altre Offerte

Palermo, Sicilia

Conduct, drive and manage country specific feasibility and/or site pre-qualification and qualification activities, which may include: -Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Cl...