Clinical Research Associate Jobs in Charleston, South Carolina

Currently, there are no Clinical Research Associate jobs available in Charleston, South Carolina which match this search. You may wish to explore similar job titles on the Healthcare jobs in South Carolina page or view related jobs below.
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Job Description : The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required)...
Job Description : The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required)...
Job Description : PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXE...
Job Description : Essential Function Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include, b...
Job Description : Essential Function Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include...
Job Description : Key Accountabilities • Assume the ability to meet the requirements of a CRA I with a high degree of proficiency and autonomy • Take responsibility for specific tasks on projects, or acts as the main CRA contact on individual projects • Train team members on selected tasks • Keep manager informed about work progress and any issues to avoid surprises. Requires some interaction...
Job Description : Essential Function Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include, b...
Job Description : The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required)...
Job Description : PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies. Given our breath of expertise and the trust placed in us by pharmaceutical companies worldwide, PAREXEL can provide you with a numb...
Job Description : PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies. Given our breath of expertise and the trust placed in us by pharmaceutical companies worldwide, PAREXEL can provide you with a numb...
Job Description : The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required)...
Job Description : The Senior CRA performs the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include, but a...
Job Description : PAREXEL International is a growing, fast-paced, global Clinical Research Organization (CRO) that has helped bring to market 49 of the top 50 selling pharmaceuticals. In fact, we have worked with all 10 of the world's top 10 pharmaceutical companies. Given our breath of expertise and the trust placed in us by pharmaceutical companies worldwide, PAREXEL can provide you with a numb...
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...
Job Description : Essential Function PAREXEL is looking for experienced Oncology Study Coordinators with RN degree to perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL's direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementati...
Job Description : The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required)...
Job Description : Essential Function Perform the clinical monitoring aspect of designated projects in accordance with study specific procedures, applicable SOPs, and regulations. Act as PAREXEL’s direct contact with assigned clinical sites and use judgment to assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites. Responsibilities include, b...
We are looking for a Senior Clinical Research Associate for an excellent client in the Kansas City, MO area. This job will have the following responsibilities: Knowledge and application of project specific protocol Consistently completes sponsor specific training and documentation Assess protocol specific and UBC SOP knowledge and assess individual's ability to perform visit type independently...
LDR Spine, a worldwide leader in innovative spine products, is seeking a dependable, adaptable, professional individual to serve as our Clinical Research Associate Level 1 in our Austin Texas Corporate Headquarters. We offer a fast paced, dynamic, and energetic atmosphere with competitive pay, good benefits, and a great working environment. We seek motivated individuals with a passion for innovati...
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...

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Healthcare Career Tools

Clinical Research Associate

Salaries

$32,614.00 - $97,000.00
Typical Salary for Clinical Research Associate in Charleston
(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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