Training Specialist |
| Position Description1. Build rapport with donors to ensure overall “customer” satisfaction with ... |
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Biological Product Specialist - Lubbock, TX / 08-5131 |
| Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and ... |
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Phlebotomist |
| Talecris Plasma Resources specialize in the collection of human plasma used in therapies that help ... |
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Pharmaceutical Sales Representative - Amarillo, Texas -4BBG2A |
| Welcome to Novartis - the company that considers its employees to be its greatest asset. Good B... |
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JOB FAIR_AMARILLO, TEXAS |
| Join us at our
JOB FAIR EVENTS
on
May 15th and May 16th
Talecris Plasma Resources is opening a ... |
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Director of Diversity and Business Development |
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Position: Director, Business Development and Diversity
Report To: C... |
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Project Manager (Analgesia experience) |
| Premier Research is a leading solutions-driven CRO leveraging our commitment to therapeutic focus ... |
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Process Engineer/Engineering Technician |
| Process Engineer/ Engineering TechnicianSpecialty pharmaceutical company near Austin, Texas is ... |
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Product Manager, Oncology |
| Asuragen is a fully integrated diagnostics company focused on molecular oncology and early ... |
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Marketing Professional |
| Marketing Professional
Key position reporting to senior marketing manager. R... |
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Home-Based CRA w/Pharma Co. - Tennessee
| Details |
Country: USA
Location: Tennessee-Nashville Nashville, TN
Total applied: 12 |
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Home-Based CRA w/Pharma Co. - Tennessee
Clinical Research Associates(CRAs)needed in Tennessee.Kelly Scientific is currently seeking Home-Based CRAs with 1 year of monitoring experience. Responsibilities would involve monitoring activities at various clinical study sites mainly in the Tennessee area. The Clinical Research Associate is accountable for investigator site management of therapeutic area sites and oversight of the clinical trial process from site selection to close out. Conducts site visits to ensure source data verification performed according to the monitoring plan, study drug accountability, and complance to GCPs, ICH guidelines, FDA regulations and applicable SOPs. Will review regulatory documents as required and preparing site visit reports. Must be able to manage multiple projects and to work well both independently and in as part of a team. May participate in study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training. JOB REQUIREMENTS:. 1-3 years of field monitoring experience as a CRA. Must be flexible to travel up to 50-75% within Tennessee . Candidate must live 1 hour of major airport. Knowledge of GCP and ICH guidelines. Good Computer skills To be considered for this position, please click on "Apply Now." Contact Information:Kelly Scientific Resources -Clinical Resource210-524-9203 or 1-800-839-0644 lopezda@kellyservices.com www.kellyscientific.com Learn more about company
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