Regional Clinical Research Associate Jobs

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1000+ Regional Clinical Research Associate jobs found on Monster.

Jobs 1 to 20 of 2060
Founded in 1963, BIOTRONIK, Inc. is a pioneer in developing innovative technologies and medical devices that save and enhance the quality of life for millions of individuals living with cardiovascular disorders. Our growing success is based on the company’s core values – Accountability, Commitment, Entrepreneurial, Integrity, Quality – thus enabling us to inspire confidence and trust in doctors an...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRAs opportunities for Phases I-IV in the U.S. and Canada. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work wit...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRAs opportunities for Phases I-IV in the U.S. and Canada. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work wit...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRAs opportunities for Phases I-IV in the U.S. and Canada. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work wit...
Are you passionate about improving the quality of human life? If so, we invite you to learn more about our home-based CRAs opportunities for Phases I-IV in the U.S. and Canada. ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work wit...
Job Description : JOB DESCRIPTION Job Title Senior Clinical Research Associate (CRA), EPD Department EPD (Clinical Operations) SBU Early Phase Essential Function Performs clinical monitoring and investigational site /relationship management for designated EPD led clinical trials in accordance with ICH GCP, applicable regulations and SOPs. Act as PAREXELs direct contact with sites and is resp...
Job Description : JOB DESCRIPTION Job Title Senior Clinical Research Associate (CRA), EPD Department EPD (Clinical Operations) SBU Early Phase Essential Function Performs clinical monitoring and investigational site /relationship management for designated EPD led clinical trials in accordance with ICH GCP, applicable regulations and SOPs. Act as PAREXELs direct contact with sites and is resp...
Job Description : JOB DESCRIPTION Job Title Senior Clinical Research Associate (CRA), EPD Department EPD (Clinical Operations) SBU Early Phase Essential Function Performs clinical monitoring and investigational site /relationship management for designated EPD led clinical trials in accordance with ICH GCP, applicable regulations and SOPs. Act as PAREXELs direct contact with sites and is resp...
We are seeking a Sr. CRA for a 6 plus month contract in either Sunnyvale or San Francisco. (Very Senior candidates would be allowed to work offsite with at least a two week orientation on site) Interested candidates should forward word doc resume with hourly salary requirements. Description Position Summary: Leads activities associated with the evaluation, initiation and management of clinical ...
InVentiv Health Clinical Hattiesburg, MS
Company Description: inVentiv Health Clinical, (formerly Smith Hanley Consulting/Medfocus/Kforce Clinical Research), is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies, offering therapeutically specialized capabilities for Phase I-IV clinical development, bioanalytical services, and strategic resourcing from a sing...
OnPoint Consulting Seattle, WA
Senior Regional CRA's West Coast CRAs Needed The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecti...
Clinical Solutions Group Chicago, IL
CRA: Core role is to verify that investigational sites are adhering to the rights and well-being of human subjects, the reported trial data are complete, accurate, and verifiable against source documents, and that the trial is conducted in compliance with the currently approved protocol, Good Clinical Practices, applicable regulations and applicable standard operating procedures (SOPs). Conduct ...
Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...
Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...
Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...
Clinical Solutions Group Houston, TX
CRA: Core role is to verify that investigational sites are adhering to the rights and well-being of human subjects, the reported trial data are complete, accurate, and verifiable against source documents, and that the trial is conducted in compliance with the currently approved protocol, Good Clinical Practices, applicable regulations and applicable standard operating procedures (SOPs). Conduct ...
Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...
Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...
Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...
Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

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