Urologyclinics
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Responsibilities Facilitate and coordinate the daily cancer clinical trial activities Coordinate the conduct of clinical trials per Good Clinical Practice and CFR guidelines Work cooperatively with on-site research staff of Investigators, Nurses, Medical Assistants. Accurate and timely trial data collection and reporting Submit regulatory documents to IRB and Sponsor Attend investigator meeting(s) Screen, track and schedule trial pts Teach subjects/patients about protocol expectations for trial visits Perform study/protocol procedures in a detailed, accurate manner Maintain study files on site Report all adverse events and SAEs Collect laboratory specimens, processing and shipping lab work Maintain communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel. Complete case report forms (CRF) and electronic data capture (EDC) for PI review and approval Coordinate site study monitor and sponsor visits Maintain study-specific supplies Prepare for study closure and archiving Knowledge of medical terminology (Oncology and Urology preferred). Knowledge of good clinical practice, FDA, OHRP, HIPAA policies. Proficiency with the Microsoft Office Suite, Google Docs, SharePoint. Meticulous attention to details
Job Qualifications At least 1 year of experience in a clinical research setting, often transitioning from an assistant role Prior experience in an oncology or urology setting preferred Performs primary duties with greater independence and has progressed to performing more advanced skill sets as directed. Some EMR (electronic medical records) experience required Some Electronic Data Capture (Rave, Oracle, Inform, etc.) experience preferred
Knowledge, Skills & Abilities Excellent organization and communications skills required. Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts. Must be detail oriented and have the ability to follow-through. Ability to effectively manage time and prioritize workload. Must practice discretion and adhere to site confidentiality guidelines at all times. Must have computer skills including the use of Microsoft Office.
Seniority level Internship
Employment type Other
Job function Research, Analyst, and Information Technology
Hospitals and Health Care
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Responsibilities Facilitate and coordinate the daily cancer clinical trial activities Coordinate the conduct of clinical trials per Good Clinical Practice and CFR guidelines Work cooperatively with on-site research staff of Investigators, Nurses, Medical Assistants. Accurate and timely trial data collection and reporting Submit regulatory documents to IRB and Sponsor Attend investigator meeting(s) Screen, track and schedule trial pts Teach subjects/patients about protocol expectations for trial visits Perform study/protocol procedures in a detailed, accurate manner Maintain study files on site Report all adverse events and SAEs Collect laboratory specimens, processing and shipping lab work Maintain communication and correspondence (by telephone, email, fax, etc.) with subjects, sponsor, monitor and other site study personnel. Complete case report forms (CRF) and electronic data capture (EDC) for PI review and approval Coordinate site study monitor and sponsor visits Maintain study-specific supplies Prepare for study closure and archiving Knowledge of medical terminology (Oncology and Urology preferred). Knowledge of good clinical practice, FDA, OHRP, HIPAA policies. Proficiency with the Microsoft Office Suite, Google Docs, SharePoint. Meticulous attention to details
Job Qualifications At least 1 year of experience in a clinical research setting, often transitioning from an assistant role Prior experience in an oncology or urology setting preferred Performs primary duties with greater independence and has progressed to performing more advanced skill sets as directed. Some EMR (electronic medical records) experience required Some Electronic Data Capture (Rave, Oracle, Inform, etc.) experience preferred
Knowledge, Skills & Abilities Excellent organization and communications skills required. Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts. Must be detail oriented and have the ability to follow-through. Ability to effectively manage time and prioritize workload. Must practice discretion and adhere to site confidentiality guidelines at all times. Must have computer skills including the use of Microsoft Office.
Seniority level Internship
Employment type Other
Job function Research, Analyst, and Information Technology
Hospitals and Health Care
Referrals increase your chances of interviewing at Urology Clinics of North Texas, PLLC by 2x
Get notified about new Clinical Research Coordinator jobs in
Dallas, TX .
Clinical Research Associate (CRA) - Dallas Study Start-Up Coordinator – Clinical Research Coordinator Experience Dallas, TX $65,000.00-$76,000.00 1 day ago
Dallas Clinical Research Project Coordinator Frisco, TX $65,000.00-$80,000.00 14 hours ago
Clinical Research Assistant I, Neurology Clinical Research Coordinator I - Rehabilitation Associate Clinical Trial Manager - PhD / Post-Doc Experience - Dallas, TX Clinical Research Assistant II, Simmons Cancer Center Clinical Research Associate - PhD in Life Sciences CRA 2, Early Clinical Development, IQVIA Dallas, TX $87,200.00-$182,000.00 14 hours ago
Clinical Research Assistant I, Neurology Dallas, TX $37,000.00-$37,000.00 3 days ago
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