Clinical Research Coordinator Resume

SUMMARY

Skilled in both PC and Mac operating systems
Experienced with SPSS, Excel, PowerPoint, Microsoft Office Suite
Experienced with ATLAS.ti and nVivo Qualitative Analytic software
Knowledge of a variety of EMR systems, including Cerner, eClinical Works, MOSAIQ, IKnowMed, Carelogic and others
Experience using Clinical Trial Data Management software
Highly skilled in Qualitative and Quantitative research methods
Experience coordinating research projects and writing research proposals
Strong organizational & time management skills
Experience recruiting and interacting with research participants
Strong ability to work independently and as part of a team
Proficient in survey development, use and analysis, including within Qualtrics
Experience leading focus groups and conducting in - depth interviews
Skilled in developing and following protocols, creating research goals and developing project timelines.

PROFESSIONAL EXPERIENCE

Confidential

Clinical Research Coordinator

Responsibilities:

Screen, recruit and enroll participants for research studies
Maintain ongoing knowledge of clinical protocols in teh fields of Oncology and Cardiology
Participate in teh informed consent process of study subjects
Maintain knowledge of Good Clinical Practice and understanding of regulatory compliance
Coordinate protocol related research procedures, study visits and follow-up care
Maintain study source documents, complete case report forms and address queries
Ensure that all trial documents maintain compliance to teh Confidential Institutional Review Board
Provide education to subjects and family regarding protocol, study intervention,
Conduct outreach efforts to inform teh public of clinical trials

Confidential

Research Assistant

Responsibilities:

Assisted with development of a linkage-to-service program aimed at assisting youth in teh Juvenile Justice system successfully enroll and engage in substance abuse treatment
Perform qualitative interviews with probation officers, substance abuse treatment providers, juveniles on probation with substance abuse problems and their caregivers to create a program linking youth on probation
Assisted with development of study protocol and manual of procedures for Family CONNECT
Recruit participants in-person, by telephone and via email for potential participation in study
Conduct literature reviews to assist with program development
Code and conduct data analysis using nVivo Qualitative Analysis Software
Maintain a high level of confidentiality

Confidential

Medicaid Compliance Analyst

Responsibilities:

Review medical records of Residential Treatment Center clients within Carelogic EHR for compliance with Medicaid regulations
Maintain ongoing knowledge of Medicaid regulations
Provide staff with support to maintain compliance

Confidential

EHR Support Associate

Responsibilities:

Provided support to upper level management with regard to implementation of teh Electronic Health Record
Provided support in all areas relating to teh implementation of teh Electronic Health Record, including support and training of all staff and employees
Assisted with workflow design, configuring and testing systems, data entry
Demonstrated experience as teh project manager at teh Residential Treatment Center in order to optimize user-knowledge and understanding of teh system