Clinical Regional Monitoring Career Research and Resources
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Avg. Salary: $50,000 · Company Rank: 4.0 out of 5
Kendle International
As a CRA for Kendle I worked in the area of Rheumatology, Gastro Intestinal disorders and Pain Management. I Performed (PSV) Pre Study Visits, (SIV) Site Initiation Visits, (IMV) Interim Monitoring Visits, (COV) Close Out Visits. I also Performed detailed review of subject records, essential documents, investigational product disposition and accountability and instruct site personnel on the procedures for the assigned tri...
Avg. Salary: $75,000 · Company Rank: Not Available
Opexa Therapeutics
While working at Opexa as a CRA I worked in the areas of CNS, Multiple Sclerosis and Immunology. I performed routine site visits, including initiation, interim and closeout visits. I performed detailed review of subject records, essential documents, investigational product disposition and accountability. I trained site personnel on procedures for the assigned trial. I worked on both Phase 1, and Phase 2b trials. I mana...
Avg. Salary: $75,000 · Company Rank: Not Available
Opexa Therapeutics
While in the position at Opexa I oversaw the manufacturing lab and five other technicians in the areas of centralized accessioning, data verification, initial processing of all specimens and the distribution of specimens for testing. I performed various chemical, biological, hematological, immunological, and microscopic tests with appropriate controls. Proficient in the separation of blood components, Cell counts (automated...
Avg. Salary: $75,000 · Company Rank: Not Available
Quintiles
• Site manager for multinational mega oncology trials. Manage fourteen protocols for twenty-two sites. • Monitor activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols. Conduct initiation, monitoring, and termination study visits. • Collaborated with multidisciplinary clinical teams to ensure project timelines are meet within monitoring plans and within budget t...
Avg. Salary: $13,500,000 · Company Rank: Not Available
PAREXEL
• Responsible for site management including tracking regulatory submissions and approvals, recruitment and enrollment, data query resolution, and supply management. • Served as Co-Clinical Lead performing such duties as addressed protocol questions,team communication point of contact, and provide site and CRAs issue escalation • Conducted qualification, initiation, monitoring, and termination study visits. • Reviewed info...
Avg. Salary: $13,500,000 · Company Rank: Not Available
INC Research
• Responsible for site management including tracking regulatory submissions and approvals, recruitment and enrollment, data query resolution, and supply management. • Served as Co-Clinical Lead performing such duties as addressed protocol questions,team communication point of contact, and provide site and CRAs issue escalation • Conducted qualification, initiation, monitoring, and termination study visits. • Reviewed info...
Avg. Salary: $13,500,000 · Company Rank: Not Available
Expression Analysis
• Analyzed gene expression using molecular assays for Affymetrix microarray analysis to target genes associated with disease and drug discovery. • Supervised lab personnel and ensured client projects were completed on time. • Implemented QC activities and consulted with clients on QC results and data related queries • Managed two research staff personnel and oversaw the day to day Affymetrix operations • Writing, editing, r...
Avg. Salary: $13,500,000 · Company Rank: Not Available
Central Coast Medical Oncology, Inc.
Brief appointment as a Clinical Research Study Coordinator managing the private side of the research department for a comprehensive cancer center in Central California. The private sector was phased out when purchased by the affiliated hospital. Study start-up, duration, close-out and follow up. All phases.
Avg. Salary: $90,000 · Company Rank: Not Available
Conversant Healthcare Systems, Inc.
Managed all aspects of site monitoring responsibilities for all phases of primarily oncology clinical trials according to SOPs, ICH guidelines and GCP, including pre-study qualification, initiation meetings, routine / interim monitoring visits, closeout visits and audits. Served as lead CRA and a resource for internal and external clients. 75-80% travel, averaging 4-5 protocols and 8-10 sites simultaneously in addition to a...
Avg. Salary: $90,000 · Company Rank: Not Available
