Research Coordinator Clinical
Resume:
Seattle, WA
Jun ****
Seattle, WA
Jun ****
Bellevue, WA, United States
Jul 2021 Current
Seattle, WA
Nov 2014 Jul 2021
Seattle, WA
Nov 2016 May 2017
Seattle, WA
Feb 2009 Nov 2012
Seattle, WA
Apr 2007 Feb 2009
Abby DeLa Cruz
Professional Summary
Highly motivated, enthusiastic, high achieving, who also has a fabulous sense of humor, CLINICAL RESEARCH COORDINATOR/CLINICAL RESEARCH ASSOCIATE with 20 years of experience in clinical healthcare in specialties such as infectious disease, neurology, oncology, allergy, immunology, otolaryngology, dermatology, nephrology, sports medicine and a first hand focus in pulmonology during the COVID-19 pandemic. Education
Pima Medical Institute - Seattle
MA-C: Medical Assistant Certification
University of Washington
Bachelor of Science: Psychology
Skills
Proficient in EDC-iMedidata RAVE, Almac, Bracket IP drug allocation -IVRS,S-ClinPhone ERT - Electronic subject diary, Infosario, Centricity All Microsoft Programs & Application Apple Programs & Applications EPIC Hyperspace EMR
Adobe PACS
Experience
Transformative Pharmaceutical Solutions
Clinical Research Coordinator
Coordinated investigators by reviewing and maintaining records of qualification for research. Supported staff by assisting with program meeting coordination. Communicated with study participants, family members, and other contacts to offer information and resources. Managed documentation, including clinical research data worksheets, shared drive, and clinical research files. Maintained required records of study activity, including case report forms, drug dispensation records, and regulatory forms. Screened potential subjects, reviewed medical records and discussed histories with physicians or nurses to determine which individuals should be admitted to each study.
Identified problems with study protocols and worked with investigators to resolve the issues. Organized and maintained the complete records for each study, including the case reports, drug dispensation records and regulatory paperwork.
Documented adverse events and data covering side effects, conferring with investigators about reports and working with oversight agencies on management of incidents.
Oversaw subject enrollment, verifying obtainment and documentation of informed consent. Coordinated efficient subject enrollment process with completely documented informed consent for each person. Swedish Medical Group SCCC Specialties
Clinical Research Coordinator/Shared Resource MA-C Prepared and maintained all supplies in exam rooms by ordering, distributing, and managing inventory. Greeted patients warmly and assisted Physician in preparing patients for exams and procedures by assessing vital signs and recording medical histories.
Administered injections and medications, dressed wounds, and collected lab specimens for tests. Performed initial response-screening following protocols under the direction of the supervising physician. Asthma, Inc. Clinical Research Center
Clinical Research Coordinator
Worked on the following studies: Astellas ASP082 Phase I; DBV Pepites, Realise, Miles Phase 3-4; Aimmune ARC003 and ARC004 Phases 3-4
Prepared, tracked, and ensured quality assurance of 50+ subject charts for visits as well as monitored enrollment, investigational product, subject identification, and temperature logs. Demonstrated patient care, medication management, transfer of data to Electronic Data Capture (EDC) systems; resolved protocol deviations promptly by reporting and communicating effectively with medical monitors Possess knowledge of standard EDC Systems, such as Trial Master Files, Target Health, and Medidata Rave. Oversee subject enrollment to ensure that informed consent is properly obtained and documented. Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies. UWMC - Otolaryngology & Audiology
Audiology Research Coordinator
Worked on Cocklear Implant and BAHA device studies Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms. Oversee subject enrollment to ensure that informed consent is properly obtained and documented. Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols. Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies Seattle Cancer Care Alliance
Clinical Research Coordinator HEME-ONC/BREAST CANCER Worked on multiple oncology IND appropriate subject based on eligibility such as screening interviews, reviews of medical records, and discussions with physicians and nurses. Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols. Assess eligibility of potential subjects through methods 1087 Lake Washington Blvd. N Apt B309, Renton, WA 98056 USA ****@****.***
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