Research Coordinator 2

Hours of Work : 40 Days Of Week : 5 Work Shift :

Job Description

Job Summary: In this highly technical, fast-paced, and challenging position, Research Coordinator 2 will collaborate with multidisciplinary team members to provide the very best care for our patients. Inclement Weather Status Not required to report Job Purpose This job will 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. Job Requirements:

Education

Bachelor’s Degree in medical or science related field, or High school diploma with 5 years of research experience Licenses and/or Certifications: Certified Clinical Research Coordinator (CCRC), or equivalent certification obtained within 2 years of hire Work Experience: 1 year of related healthcare experience with bachelors degree or 5 years of research experience with high school diploma Related Work Experience and Other Skills: Bilingual skills (Spanish and English), preferred Experience in medical terminology, preferred Job Roles: 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 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 Other duties as assigned Age Specific Care Considerations: ☒ Adults: 18+ years – 35 years ☒ Adults: 35+ years – 65 years ☒ Adults: 65+ years ☒ Children A: 18+ months – 3 years ☒ Children B: 3+ years – 5 years ☒ Children C: 5+ years – 12 years ☒ Children D: 12+ years – 18 years ☒ Infants: 0 – 18 months Methodist…

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