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PharmaNet-Memphis, TN, 37501
We currently have openings for Regional, home-based Clinical Research Associates throughout the United States. Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (up to 80% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Generate study specific documentation including monitoring trip reports, telephone contact reports, site correspondence, and expense reports. Recruit investigators for participation in clinical trials Conduct project feasibility assessments Negotiate study budgets with investigators Obtain, review for appropr...
Clinical Research Associate Jobs in Memphis, Tennessee Jobs
Quintiles Transnational | Memphis, TN, 37501 | 1
The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team in our Southeast region. The clinical research associate monitors activities at clinical study sites to assure adherence to Good Cli...
PharmaNet | Memphis, TN, 37501 | >1
We currently have openings for Regional, home-based Clinical Research Associates throughout the United States. Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (up to 80% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Generate study specific documentation including monitoring trip reports, telephone contact reports, site correspondence, and expense reports. Recruit investigators for participation in clinical trials Conduct project feasibility assessments Negotiate study budgets with investigators Obtain, review for appropr...
PharmaNet Jobs
PharmaNet | Princeton, NJ, 08540 | >1
Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g. study specific guidelines and procedures, case report forms, and monitoring conventions) at Investigators’ Meetings Prepare and process S...
PharmaNet | Blue Bell, PA | 3
- Conduct Good Clinical Practice (GCP) audits of investigator sites, vendors, databases and study reports - Provide Quality Assurance (QA) review of draft tables and listings for study reports - Conduct QA evaluation of internal processes - Provide project management oversight for compliance-related tasks and programs - Present compliance requirements at investigator meetings - Provide training to clinical research staff on GCP regulations - Train auditing staff - Provide input and assistance to Business Development for time and cost proposal development - Enter audit observations into Corr...
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