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DALLAS VA RESEARCH CORPORATION
Dallas, TX, United States
Education and Experience Requirements: Must be eligible to work in the U.S.; H1b visa holders are ineligible More than 4 years of research experience; or 3+ years of research experience and a Bachelor Degree in a relevant area; or 3+ years of research experience and an LVN; or Greater than 1 year of research experience and a Masters Degree or
Job Source: DALLAS VA RESEARCH CORPORATIONWILLIAM R LUMRY MD PA
Dallas, TX, United States
Job Description Job Description Seeking experienced Clinical Research Coordinator to assist with ongoing clinical trials in the asthma and allergy space. Experience witn regulatory, patient recruitment and assessment, electronic data capture and conduct of clinical trial required. Company Description We are a Allergy & Immunology office, we study
Job Source: WILLIAM R LUMRY MD PAALLERGY PARTNERS
Dallas, TX, United States
Job Details Job Location 70-00-Dallas - Dallas, TX Description JOB SUMMARY: clinical coordination of all aspects of adult and/or pediatric clinical research trials primarily sponsored by pharmaceutical companies. Responsibilities include, but are not limited to, the following: Clinical Support Performs all aspects of research related job duti
Job Source: ALLERGY PARTNERSDALLAS VA RESEARCH CORPORATION
Dallas
Job Description Job Description Education and Experience Requirements: Must be eligible to work in the U.S.; H1b visa holders are ineligible More than 4 years of research experience; or 3+ years of research experience and a Bachelor Degree in a relevant area; or 3+ years of research experience and an LVN; or Greater than 1 year of research exper
Job Source: DALLAS VA RESEARCH CORPORATIONUT Southwestern Medical Center
Dallas, TX, United States
Clinical Research Coordinator I, Internal Medicine - Pulmonary Why UT Southwestern? With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits fo
Job Source: UT Southwestern Medical CenterEmVenio Research
Dallas
Job Description Job Description ABOUT EMVENIO RESEARCH: EmVenio Research delivers localized trial access to diverse and underserved communities. We empower patients and embrace communities on their terms. Our research solutions cultivate a sustainable local ecosystem that benefits all stakeholders. Removing barriers and unlocking doors to innova
Job Source: EmVenio ResearchSearch Influence
Dallas, TX, United States
ABOUT EMVENIO RESEARCH: EmVenio Research delivers localized trial access to diverse and underserved communities. We empower patients and embrace communities on their terms. Our research solutions cultivate a sustainable local ecosystem that benefits all stakeholders. Removing barriers and unlocking doors to innovation reduces risk and time associat
Job Source: Search InfluenceMethodist Health System
Dallas
**Hours of Work :** 08:00-16:30 **Days Of Week :** Monday - Friday **Work Shift :** **Job Description :** Your Job: This job will support of all phases of the research process in support of Trauma and General Surgery research protocols. The responsibilities will include support of protocol and manuscript development process, coordination of data co
Job Source: Methodist Health SystemMesquite
Job Description Job Description EXPERIENCE IN CLINICAL RESEARCH IS A MUST
The Clinical Research Coordinator is responsible for managing the daily operations of a clinical investigation. This position will manage multiple, sponsored (Phase I, II, III, IV, and V) clinical trials for many indications within primary care.
The Essential Job Functions are :
Maintain a detailed knowledge of all study protocols in order to complete all study activities correctly and completely
Recruit and screen patients for assigned studies
Provide instructions and education to subjects to ensure proper protocol compliance
Complete visit procedures including, but not limited to, obtaining vital signs measurements, performing ECG's, and collecting blood samples for processing and shipment to the appropriate lab facility
Notify the Investigator of all adverse events
Report all serious adverse events in compliance with FDA regulations and sponsor requirements
Provide the Sponsor with accurate and complete documentation and information
Complete and maintain accurate, legible and complete source documents and case report forms per FDA guidelines and Sponsor requirements
Prepare for FDA audit by ensuring all documentation and case report forms are available and complete. Ensure the rights, safety and welfare of all subjects at all times
Ensure that each subject has completed the informed consent process, following GCP guidelines, and has consented to participate before any study related procedures are performed
Provide subjects education on an ongoing basis throughout their participation in the protocol
Report all adverse events to the Investigator, Sponsor and IRB
Complete all relevant site-level and study-level logs in a timely manner
Utilize a team approach including the PI, Sub-Investigators, Site Manager, other Coordinators and Research Assistants
Act as a liaison to ensure complete and accurate communication between physicians, sponsors and subjects. Work in a collaborative, effective manner with the Sponsor to meet research objectives
Understand all internal policies and procedures approved by the Medical Director, Site Manager, and any other departments
Job Type: Full-time
Experience:
Clinical research coordinator: 2 year (Required)
Phlebotomy: 1 year (Required)
Vital Signs: 1 year (Required)
Education:
High school or equivalent (Required)
License:
CCRC/CCRP (Preferred)
Clinical Research Coordinator jobs in Mesquite
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