Clinical Research Associate Jobs in Massachusetts

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51 Massachusetts Clinical Research Associate jobs found on Monster.

Jobs 1 to 20 of 51
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...
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, b...
Job Description : Duties : Plan, direct and develop clinical trial activities in an FDA 21 CFR Part 11 regulated environment on Lupus and other clinical studies. Determine goals and strategies with clinical project management and trial sponsors to ensure compliance with clinical trials deliverables. Manage clinical trial information, monitoring and analysis using sophisticated technologies includ...
Job Description : ***Replacement for future turnover*** 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 c...
Job Description : ***Replacement for future turnover*** 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 clin...
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 : 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 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 : 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...
Responsibilities: Contributes to the preparation of clinical protocols, informed consent form templates, study manuals and/or instructions, case report forms, pharmacy manuals. Identifies investigators and investigational sites. Collects and analyzes feasibility questionnaires for site selection purposes. Develops study newsletter content and maintains study FAQ logs. Assists with the oversigh...
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 : 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...
Duties : Plan, direct and develop clinical trial activities in an FDA 21 CFR Part 11 regulated environment on Lupus and other clinical studies. Determine goals and strategies with clinical project management and trial sponsors to ensure compliance with clinical trials deliverables. Manage clinical trial information, monitoring and analysis using sophisticated technologies including Perceptive View...
Under the general supervision and direction of the Senior Clinical Research Associate, is responsible for coordinating research studies for the Clinical Research Program. Also responsible for generating reports and statistical information relating to these research studies and research in general and support staff of the Lahey Clinic to the conduct of research. Essential Duties & Responsibilities...
The primary responsibility of a Senior Clinical Research Associate is to ensure that the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP, and with applicable regulatory requirements. The Senior CRA will also ensure that the rights and well-being of human subjects are protected and that the reported trial data is accurate, complete, and verifiable f...
The primary responsibility of a Clinical Research Associate II is to ensure that the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP, and with applicable regulatory requirements. The CRA II will also ensure that the rights and well-being of human subjects are protected and that the reported trial data is accurate, complete, and verifiable from sour...
PURPOSE AND SCOPE: Provides support to the FMS Clinical Studies Department and the contract research organization (CRO) by monitoring and tracking the progress of clinical study activity at FMS and non-FMS research sites ensuring compliance with all pertinent agency, state and federal regulatory requirements. Ensures the Trial Master File is maintained and ready for FDA Inspection. Provides suppo...

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Healthcare Career Tools

Clinical Research Associate

Salaries

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