Regional Clinical Research Associate Jobs

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1000+ Regional Clinical Research Associate jobs found on Monster.

Jobs 1 to 20 of 1348
Requisition ID 25089BR Title Regional Clinical Research Associate (CRA)- Houston, TX 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...
A pharmaceutical company is seeking a Regional CRA to support coverage primarily in the Chicago Area. This opportunity is initially a 12 month contract with the option to extend. This position is seeking someone with 8 or more years of independent field monitoring experience within a CRO or sponsor environment. Regional CRAs will be responsible for handling multiple studies and sites simultaneous...
Requisition ID 25178BR Title In-House Clinical Research Associate (CRA) Job Category Clinical Trial Management Job Description PURPOSE: Responsible for the support of assigned sites in accordance with 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 C...
Job Description : 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 responsible for conduct of both on-site visits and remote/off-site communication/site management. Responsible to assess and ensure th...
Senior Clinical Research Associate Home based throughout the SouthWest. TEXAS Preferred. Multiple positions available. If you have at least 5 full years of regional field monitoring, Provident Research is looking for you! This role is for individuals to be responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues ...
Senior Clinical Research Associate Home based throughout the West Coast. Multiple positions available. If you have at least 5 full years of regional field monitoring, Provident Research is looking for you! This role is for individuals to be responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues within the Organ...
Senior Clinical Research Associate Home based throughout the SouthWest Coast. Multiple positions available. If you have at least 5 full years of regional field monitoring, Provident Research is looking for you! This role is for individuals to be responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues within the ...
Senior Clinical Research Associate Home based throughout the Mid West Coast. Multiple positions available. If you have at least 5 full years of regional field monitoring, Provident Research is looking for you! This role is for individuals to be responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues within the O...
Theorem Clinical Research Sacramento, CA, 94204
Lead Clinical Research Associate (LCRA) *These are remote, home-based opportunities open to most US locations. The Lead CRA (LCRA) is responsible for the management of day-to-day aspects of study sites and CRA activities for the assigned study or studies. The LCRA, in concert with the Project Leader, is accountable for the timely, quality, satisfactory, and cost-effective completion of the client...
Primary Responsibilities SGS is much more than just a place to work. It's a place where you can put your innovative thinking and business skills into high gear and grow. The Clinical Research Associate is responsible for the organization, coordination, administrative management, monitoring and site management of national and international clinical trials (phase I-IV) according to ICH-GCP, EU CTD ...
NOVO Nordisk Houston, NJ
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: ...
Job Description: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to inVentiv Health Clinical SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and admini...
Job Description: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to inVentiv Health Clinical SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and admini...
Job Description: Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to inVentiv Health Clinical SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and admini...
Location - Must be located in LA due to local site visits Minimum REQUIREMENTS: At least three years or more monitoring clinical trials as a CRA - please do not apply unless you have clinical trial monitoring experience as a CRA Must have Oncology experience with clinical trials Bachelor’s degree in life sciences or related field or certification in a related allied health profession from an a...
Job Description A highly reputable & distinguished corporation is currently looking for Regional Clinical Research Associates needed (location) Job Description • Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (60% travel with 75% at peak times) for GCP compliance according to company SOPs and/or client guidelines • Recruit investigators for participation i...
SGS is much more than just a place to work. It's a place where you can put your innovative thinking and business skills into high gear and grow. The Clinical Research Associate is responsible for the organization, coordination, administrative management, monitoring and site management of national and international clinical trials (phase I-IV) according to ICH-GCP, EU CTD or FDA CFR21, whichever i...
SGS is much more than just a place to work. It's a place where you can put your innovative thinking and business skills into high gear and grow. The Clinical Research Associate is responsible for the organization, coordination, administrative management, monitoring and site management of national and international clinical trials (phase I-IV) according to ICH-GCP, EU CTD or FDA CFR21, whichever i...
SGS is much more than just a place to work. It's a place where you can put your innovative thinking and business skills into high gear and grow. The Clinical Research Associate is responsible for the organization, coordination, administrative management, monitoring and site management of national and international clinical trials (phase I-IV) according to ICH-GCP, EU CTD or FDA CFR21, whichever i...
This part time position will be working approximately 56 hours per pay period. Accountability Objectives: Under limited supervision, organizes and coordinates the development of materials for the Breast Cancer Outcomes study, Michigan Breast Oncology Quality Initiative (MiBOQI). Maintains the data management system for data entry and tracking in the NCCN Breast Cancer database. Completes and anal...

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Healthcare Career Tools

Clinical Research Associate

Salaries

$32,614.00 - $97,000.00
Typical Salary for Clinical Research Associate
(339 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
47.8%
Master's
29.9%
Doctorate
12.5%
Associates
5.4%
(224 Respondents)
Source: Monster.com Careerbenchmarking Tool

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