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WILLIAM 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 PARTNERSSalma Mazhar MD PA
Mesquite
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
Job Source: Salma Mazhar MD PADALLAS 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 CORPORATIONEPW Curesearch LLC
Plano
Job Description Job Description A multi-year Clinical Research Coordinator (CRC) position is available at our research site in Plano, TX with an initial focus on an active pulmonary study from a major pharmaceutical sponsor. Working independently under the Research Program Manager, the CRC will be responsible for carrying out clinical research st
Job Source: EPW Curesearch LLCSearch 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 InfluenceDM Clinical Research
Irving
Job Description Job Description Clinical Research Coordinator III A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' ex
Job Source: DM Clinical ResearchDM Clinical Research
Irving
Job Description Job Description Clinic Research Coordinator II The Clinical Research Coordinator II , will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure
Job Source: DM Clinical ResearchDallas
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 experience and a Masters Degree or Ph.D. in a relevant area; or
SoCRA or ACRP Certification : Highly desirable and counts as one year of experience
Software Requirements : Experience with Microsoft Office and research database products
Responsibilities : The position works under light supervision of the Principal Investigator or more experienced coordinator. The Coordinator is responsible for conducting procedures for one or more research studies. The Coordinator may supervise less-experienced Coordinators or Research Assistants. They will maintain the protection of human subjects while meeting the research goals of each project. Will consistently exhibit behavior and communication skills that demonstrate DVARC’s commitment to superior customer service and dedication to the care of our veterans.
Supervisors : VANTHCS Principal Investigator, DVARC Coordinator Manager and/or Senior Coordinators
Duties :
Assists in the design of research survey forms to capture required participant information
Interviews study participants and/or family members to gather research information
3. Reviews exclusion/inclusion criteria with the Principal Investigator or Senior Coordinator to ensure subject eligibility
4. Conducts interviews to confirm study eligibility and willingness to follow and complete study procedures and visits
5. Performs consent process with patients, ensuring inclusion and exclusion criteria are met, taking responsibility for all aspects of research completeness, enrollment notes, administrative duties and data entry
6. Develops, coordinates and reviews research study procedures to ensure receipt, completeness and accuracy of study data
7. Coordinates, with the assistance of higher grade staff, all regulatory requirements such as preparing safety reports, adverse event paperwork, FDA compliance, sponsor monitoring and logs, laboratory standards, and maintenance of databases related to regulatory requirements
8. May assist with the study budget and negotiation of participant payments
9. Monitors budget, prepares reimbursement requests, approves expenditures and reconciles study accounts
10. Prepares and submits information in the Case Report Form and submits a billing matrix for funding source and submits to DVARC
11. Prepares statistical reports, charts and graphs as required
12. Assists in preparation of annual reports for federal, state, and local agencies
13. Informs IRB of amendments to research studies
14. Coordinates collection and data management of national research studies from multiple projects by interacting with internal and external research data managers, patients, and physicians for coordination of tissue samples, lab data and protocols, and other statistical information concerning research study subjects
16. Serves as primary liaison and prepares annual reports for federal, state, and/or local agencies.
17. Informs Institutional Review Board of amendments to research studies, and prepares protocols and detailed summaries in lay terms of any new research study
18. May provide full supervision to personnel of lower grades
19. May perform lower risk, less complicated procedures in studies, if directed by Principal Investigator
Clinical Research Coordinator jobs in Dallas
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