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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 Houston 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 Resource 210-524-9203 or 1-800-839-0644 lopezda@kellyservices.com www.kellyscientific.com