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Regional Clinical Research Associate Jobs

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May independently design, plan, implement, and provide overall direction of clinical research projects. Manage all aspects of unblinded assigned clinical studies to ensure studies are completed on time, within budget, and in compliance with Good Clinical Practice (GCP), government regulations, and overall clinical objectives. Develop protocols, investigator brochures, and study reports, and assist...

Daily activities will vary depending on the clinical phase of the program. Will have responsibility for managing more than one project. Determine methods and procedures for performing new assignments. The Senior CRA may oversee the activities of CTAs and CRAs. Manage contract research organization (CRO) personnel and study sites to ensure studies are completed on time, within budget, and in compl...

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...

We are working with a client who is seeking Regional Clinical Research Associates for a PERM opportunity. Ideal locations are home-based in CA, Texas, and throughout the Midwest. Oncology and / or Phase I experience are pluses. Travel is 65%-70%. MUST have at least 4 years of field monitoring experience. The client would like to hire monitors who can start sometime in September. Please apply her o...

We are working with a client who is seeking Regional Clinical Research Associates for a PERM opportunity. Ideal locations are home-based in CA, Texas, and throughout the Midwest.Oncology and / or Phase I experience are pluses. Travel is 65%-70%.MUST have at least 4 years of field monitoring experience. The client would like to hire monitors who can start sometime in September.Please apply her or c...

Intercept is an exciting new company, headquartered in the US. We are building a platform to become a credible partner in progressive, non-viral Liver Diseases to physicians, patients, payers and the broader scientific community. As Intercept develops towards commercialization in 2016, we are creating a European organization full of people who are committed to bringing new innovation in Liver Dise...

POSITION SUMMARY: The position offers the opportunity to be involved in all phases of clinical study development - from protocol planning, through execution and the preparation of study reports and regulatory NDA and MAA filings. The position requires adaptability and the capacity to ‘own’ tasks, problem solve and to see projects through to their end. ESSENTIAL FUNCTIONS: To perform this job su...

POSITION SUMMARY: The position offers the opportunity to be involved in all phases of clinical study development - from protocol planning, through execution and the preparation of study reports and regulatory NDA and MAA filings. The position requires adaptability and the capacity to ‘own’ tasks, problem solve and to see projects through to their end. ESSENTIAL FUNCTIONS: To perform this job su...

POSITION SUMMARY: The position offers the opportunity to be involved in all phases of clinical study development - from protocol planning, through execution and the preparation of study reports and regulatory NDA and MAA filings. The position requires adaptability and the capacity to ‘own’ tasks, problem solve and to see projects through to their end. ESSENTIAL FUNCTIONS: To perform this job su...

POSITION SUMMARY: The position offers the opportunity to be involved in all phases of clinical study development - from protocol planning, through execution and the preparation of study reports and regulatory NDA and MAA filings. The position requires adaptability and the capacity to ‘own’ tasks, problem solve and to see projects through to their end. ESSENTIAL FUNCTIONS: To perform this job su...

Intercept is an exciting new company, headquartered in the US. We are building a platform to become a credible partner in progressive, non-viral Liver Diseases to physicians, patients, payers and the broader scientific community. As Intercept develops towards commercialization in 2016, we are creating a European organization full of people who are committed to bringing new innovation in Liver Dise...

POSITION SUMMARY: The position offers the opportunity to be involved in all phases of clinical study development - from protocol planning, through execution and the preparation of study reports and regulatory NDA and MAA filings. The position requires adaptability and the capacity to ‘own’ tasks, problem solve and to see projects through to their end. ESSENTIAL FUNCTIONS: To perform this job su...

Requisition ID 32435BR Title Regional Clinical Research Associate (CRA)-Biopharm-LA/Orange County Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regul...

Requisition ID 32436BR Title Regional Clinical Research Associate (CRA) - Cleveland, OH Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and...

Requisition ID 32438BR Title Regional Clinical Research Associate (CRA) - Sacramento, CA Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations an...

Requisition ID 32439BR Title Regional Clinical Research Associate (CRA) - Pittsburgh, PA Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations an...

Requisition ID 32369BR Title Regional Clinical Research Associate (CRA) - Irvine, CA Job Category Clinical Trial Management Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SO...

PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR.RELATIONSHIPS: Rep...

PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR.RELATIONSHIPS: Rep...

PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaboration with other members within Clinical Trial Management (CTM) and with various representatives within CMR.RELATIONSHIPS: Rep...