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DM 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 ResearchDM 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 Unblinded Clinical Research Coordinator II Unblinded Clinical Research Coordinator II will be responsible for dispensing Investigational Products (IP) as part of clinical research trials. DUTIES & RESPONSIBILITIES Compound and dispense prescribed IP as needed by Sponsor approved protocol Study IP management Pr
Job Source: DM Clinical ResearchUS Oncology, Inc
bedford
RN Sr-Clinical Research Overview Texas Oncology is looking for a Full-time Clinical Research Nurse (RN) to join our team! This position will support the Bedford location. This is a Full-time Monday-Friday 8:30am-5pm position with no weekends, call, or major holidays. Texas Oncology is the largest community oncology provider in the country and h
Job Source: US Oncology, IncMethodist 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 SystemSource One Technical Solutions
Fort Worth, TX, United States
Source One is a consulting services company and we're currently looking for the following individual to work as a consultant with our direct client, a Global Medical Device client. Location: Remote (however, candidate will need to be in specific states as they may occasionally have to go into the office.) States: CA, AZ, IL, WA, IL, NC, FL, SC, GA,
Job Source: Source One Technical SolutionsNCH Healthcare
Colleyville, TX, United States
Job Summary The Clinical Research Nurse works closely with physicians and other clinical team members to execute clinical research projects in an acute care/inpatient, ambulatory or ancillary care setting. This includes project initiation, patient enrollment, managing research-related patient care, tracking progress, and coordinating study particip
Job Source: NCH HealthcareRandstad USA
Fort Worth, TX, United States
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of position
Job Source: Randstad USAArlington
Job Description Job Description Duties a CRC is required to perform include the following core functions, but are not all inclusive of:
· Direct interaction with and caring for human research participants
· Evaluate patients for inclusion and exclusions criteria on multiple protocols
· Schedule and coordinate all subject visits from screening to final follow up
· Perform chart review to evaluate for inclusion/exclusion criteria
· Perform venipuncture using universal precautions
· Perform EKG, vitals and any required trial specific procedures
· Ensure accuracy of data at each visit
· Adhere to GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs guidelines
· Understand and working knowledge of being “Audit Ready at all times”
· Maintain regulatory documents to ensure most current documents are being utilized
· Support team members and cross-train to maintain knowledge of all delegated trials
· Create and maintain project timelines
· Maintain good relationships with Principal Investigator, site staff, patients and Sponsor/CRO
· Coordinate, record and manage subject data by maintaining accurate and complete source
· Complete case report forms and queries in a timely manner, per SOP guidelines
· Maintain records of receipt, storage and distribution of investigational product
· Attend and facilitate sponsor visits and audits
· Maintain accurate records of subject visits, to complete monthly study invoicing, per CTA
· Complete budget and CTA initial negotiation and amendments as necessary
Salary is based on experience.'
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Work Remotely
No
CLINICAL RESEARCH COORDINATOR jobs in Arlington
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