Careers | Methodist Health System

Careers

Career opportunities at Methodist Health System

Research Coordinator 2

Job Title
Research Coordinator 2
Job ID
27658094
Location
Dallas,  TX 75265
Other Location
Description

Your Job


In this highly technical, fast-paced, and challenging position, you'll collaborate with multidisciplinary team members to provide the very best care for our patients. The Research Coordinator 2 perform coordination of all phases of the research process. The Responsibilities will include attainment of the approval process required, coordination of data collection, management, patient follow-up and tracking.

Your Job Requirements

  • Bachelor degree or Medical Assistant in appropriate discipline
  • RN Degree preferred
  • Medical Assistant Certification, and/or a Certified Clinical Research Coordinator (CCRC) required
  • LVN or RN license, preferred
  • 2 or more years of related experience

 Your Job Responsibilities :

  • Available to sponsor monitors upon study site visits
  • Follow patients throughout study
  • Maintain statistical information
  • Following all rules and regulations from the FDA, IRB, and other agencies designated
    by the sponsors.
  • Initiating and maintenance of IRB regulations (including completion of all required documents for submitting for IRB approval)
  • Coordinating all phases of assigned clinical trials: Ensuring protocol compliance;
  • Collecting, interpreting and reporting all clinical data
  • Maintaining drug inventory
  • Preparing charts for clinic: Pull charts prior to clinic visit
  • Organization of data pertinent to clinic visit
  • Completion of case report forms
  • Attending regular meetings with physicians and other research staff in
    order to get updates on the progress of the research studies/patients on treatment
  • Track lab results and obtains final result for NP or Physicians to review: Makes sure lab
    results are received in a timely manner
  • Triaging all phone calls for patients (research related or standard of care) considering
    treatment, on treatment or being followed after treatment
  • Assistance with writing protocols
  • Performing study related procedures (lab processing, etc)
  • Follow patients throughout study
  • Developing a working knowledge of disease process under study
  • Performing rating scales and/or tools under investigation
  • Communicate clearly and openly
  • Build relationships to promote a collaborative environment
  • Be accountable for your performance
  • Always look for ways to improve the patient experience
  • Take initiative for your professional growth
  • Be engaged and eager to build a winning team

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