Clinical Research Coordinator
Resume:
Arvice C. Carroway, Jr.
Accel Research Sites
Decatur, GA.
**********@***.***
Clinical Research Areas of Therapeutic Experiences:
Hematology, Oncology, Hepatology, Gastroenterology, Neurology, Endocrinology, Psychology, Cardiology, Pediatrics/Adolescents, Vaccines and Phases 1-4 of clinical trials.
Employment History:
June. 2021- present Accel Research Sites/NeuroStudies Decatur, GA.
Clinical Research Site Manager/CRC/Regulatory (Study Start-up)
Sept. 2014- present Atlanta Technical College
Adjunct College Professor Atlanta, GA. Health and Public safety courses (adjunct) LPN, Medical Assistants, Hemo-dialysis, Phlebotomy, Medical Terminology, A & P I/II, EMT/EMS, Introduction to Healthcare and Pharmacy Technician.
May. 2020-2021 Rare Disease Research Atlanta, GA.
Clinical Research Coordinator
Sept. 2019-May 2020 Center for Rare Neurological Diseases Norcross, GA.
Clinical Research Coordinator III
Exp. With NASH, PBC, HEP. C etc…
Nov. 2015-Sept.2019 Digestive Healthcare of GA. Atlanta, GA.
Clinical Research Coordinator I
Aug. 2013-2014 Anthem College (campus closed) Atlanta, GA.
MA Program Chair/Online Instructor
Feb. 2008- Aug. 2013 Sanford Brown College Atlanta, GA.
Team Leader/Instructor (Medical Assisting)(Phlebotomy/Hemo-dialysis)
Education:
King’s Career College (LPN)(graduated January 2018)
University of Phoenix AS Healthcare Management (graduate of 2014)
Lincoln Technical College (Associate of Applied Science) Medical Assisting 2007
Certified Phlebotomist (current)
West Florence High School (diploma) 1992
CPR/BLS Certified (1999-current)
CPR AHA/ARC Instructor (current)
GCP Training (current)
IATA Training (current)
Research/Management Description:
●Administrative/clinical manage an average of seven to eight trials
●Managing staff schedule
●EDC (Oracle, Greenway, Varian, EMR, IBM, Medidata)
●Completing the feasibility reports
●Patient monitoring
●Finances and Budgeting
●PSVs/SIVs
●Phase 1-4 studies
●Adhere to Good Clinical Practices and the study protocols
●Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials.
●Reviewing contracts/selection of other studies
●Prepare regulatory docs for initiation of clinical trials
●Discuss study protocols with patients/verify the informed consent documentation
●Provide patient with written communication of their participation
●Administer questionnaires/diaries per protocol/Analysis skills
●Complete and maintain case report forms per FDA guidelines
●Ensure patient’s referring physician receives notification of patient’s participation in studies as requested via patient
●Documentation review and data collection
●Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study
●Ensure compliance of protocol documents, local SOPs and regulations
●Dispense study medications per protocol
●Demonstrate consistent professional conduct and meticulous attention to detail
●Collect, process, and ship blood/urine specimens
●Perform Infusions (IV placement), ECGs, Fibroscans and collect all vital signs
●Schedule all patient research visits and procedures consistent with protocol requirements
●Ensure the filing and maintenance of all regulatory documents
●Screen all laboratory results when received (per protocol)
●Ensure all lab results are given to the appropriate PI/SubI
●Distinguish between SAE/AE
●Work closely with PI and SubI regarding the entire study and patients
●Host meetings with PI and SubI weekly
●Complete queries as they are posted
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