Clinical Research Associate Jobs

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942 Clinical Research Associate jobs found on Monster.

Jobs 1 to 20 of 942
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)...
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...
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...
Basic Function and Scope of the Position: Provides clinical support for diagnostic product development to achieve clearances and approvals in the US and internationally. Provides clinical trial site management and assures successful conduct of clinical studies consistent with applicable regulations, guidelines and procedures. Reviews, assesses and interprets data from ongoing and completed studie...
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...
Summary 
 Designs, plans, and implements clinical research projects. Participates in and coordinates the protocol and final clinical study report writing efforts. Conducts pre-study, initiation, and interim clinical study monitoring visits. Coordinates activities of clinical site to ensure compliance with protocol and overall clinical objectives. Maintains a high level of professional expertise t...
Vanda Pharmaceuticals Inc. Washington, DC, 20037
Position Description & Responsibilities The Clinical Research Associate (CRA) is part of the Clinical Development Team and will be assigned to project teams. They would be responsible for assisting the clinical study team in the design, execution and reporting of clinical studies. Roles and responsibilities include, but are not limited to, the following: Participating in the study development an...
Job Description Position: Full-time Clinical Research Associate (Data Manager) in Pediatric Hematology, Oncology and Stem Cell Transplantation 1. Job Objectives: - Ensure compliance with the implementation, documentation and reporting procedures for medical/scientific research in the Division of Pediatric Hematology,Oncologyand Stem Cell Transplantation at New York Medical College/Westchester M...
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...
Our client is currently seeking 2 Clinical Research Associates. One will have responsibility for travel to Cincinnati and the other will have St Louis. Temp to perm position. This job will have the following responsibilities: In House CRA responsibilities. Accountable to collect and review regulatory documentation to support study start up activities, including ordering site supplies and stud...
Preference for NE regions. The Senior Clinical Research Associate (CRA)/Principal CRA - Site Intelligence - Activation (Study Start Up) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures with a primary focus on site selection and initiati...
We are seeking an experienced, high caliber Sr. Clinical Research Associate. This role is responsible for working independently with minimal guidance and direction, assists in the planning and conduct of SJM clinical studies. Ensure compliance to study protocol, domestic and international Good Clinical Practices, applicable regulatory standards, and SJM Standard Operating Procedures. Able to solve...
SENIOR CLINICAL RESEARCH ASSOCIATE WITH CLINICAL TRIAL RESEARCH EXPERIENCE REQUIREMENT #14-01108 RECRUITER: ANITA JORDAN JOB LOCATION: PARSIPPANY, NJ OCTOBER 9, 2014 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Under general direction, monitors the initiation and performance of clinical trials at external research sites to assure compliance with all st...
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...
Requisition ID 24465BR Title Regional Clinical Research Associate (CRA)- Orlando, FL 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...
Requisition ID 24467BR Title Lead Clinical Research Associate (CRA) Job Category Clinical Trial Management Job Description PURPOSE: Responsible for the performance of assigned sites in accordance with Good Clinical Practice (GCP), ICH guidelines and federal regulations. Responsible for operational aspects of planning and management of site performance in accordance with departmental productivi...
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...
JOB SUMMARY: Responsible for monitoring and or management of the clinical trial monitoring function of Seattle Genetics clinical trials. This position focuses on coordination of all activities required to initiate, maintain and close -out clinical trials. May lead a clinical trial or selected activities. DETAILED DUTIES & RESPONSIBILITIES TYPICALLY INCLUDE: · May act as Protocol Lead on one or ...

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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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