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Click here or scroll down to respond to this candidateCandidate's Name
EMAIL AVAILABLEPHONE NUMBER AVAILABLEPROFESSIONAL SUMMARYResearch Coordinator with 20+ years of proven experience in clinical research coordination and leadership. Possess extensive knowledge in Database Management, Clinical Study Management, and Patient Outreach/Management with a strong and comprehensive background in hands-on experience in maintaining and preprocessing data for analysis & interpretation, comprehensive knowledge of ensuring proper storage, linkage and cleaning of collected health data, professional approach in supporting data verification, highly qualified in tracking records and maintaining clinical study subject information including, well acquainted with assisting program designs and maintenance of survey instruments. I have a complete understanding of administering surveys to study participants as directed. Proficient in managing/supervising with the ability to plan, communicate, delegate, coordinate tasks, problem solve, motivate and make executive decisions to build teams, develop employees, evaluate them, and accomplish company goals.Written CommunicationPatient RelationsTraining/MentoringDatabase ManagementLeadership/SupervisorClinical ResearchProject ManagementInterpersonal CommunicationClinical Database CollectionPROFESSIONAL EXPERIENCEJohns Hopkins Pulmonary Research Program Research Program SupervisorJanuary 2022 - May 2024As the Research Program Supervisor (RPS) Responsible for overseeing the research clinical activities including: participant recruitment, screening of potential COPD participants, performing clinic visits that include administering questionnaires, blood draws, spirometry and other breathing tests, while ensuring the study is in compliance with IRB and study eligibility criteria. Supervise (Research Program Assistants and Coordinators) working under multiple research studies. Coordinated with clinical staff and the data team acting as a liaison between them and the Research Project Manager and/or Principal Investigator. My supervising duties consisted of but were not limited to hiring/writing job descriptions, training, and evaluating research staff meeting with staff members individually to on work-related performance issues; maintaining time records and weekly hour submissions; tracked, maintained and prepared Travel Expense Reports for staff; trained clinical staff on IRB policy and study procedures depending on project protocols ensuring the quality of data collection and participant safety; and arranging training courses for new hires (IRB compliance, EPIC, CRMS, Spirometry, etc.). Participated in weekly progress meetings of current research projects to report on recruitment progress and resolve problems. Assisted in developing and maintaining appropriate databases for current and future studies. Conducted interviews over the phone or in person to determine eligibility for a research study. Responsible for IRB submissions (applications, amendments and annual renewals), verification and maintenance of necessary protocol specific information in paper and electronic format to meet requirements of IRB and all relevant regulatory bodies.Johns Hopkins University, Department of Mental HealthResearch CoordinatorMay 2018 - December 2021As the Research Coordinator for the Johns Hopkins School of Public Health, my role is to assist with the logistics of protocol to ensure that the study is being conducted accurately. Communicate on behalf of faculty, via email and phone, with research collaborators, divisional offices, and IRB. Responsible for organizing and assisting with the design methods of data storage for sensitive and confidential information, i.e., paper logs, scanning, and electronic reports, files and databases. Prepare correspondence to study participants and co-investigators. Perform administrative duties by completing reports to IRB, performing special projects, and assisting in the preparation of grant proposals, applications, continuations, and other correspondence by preparing and tracking forms specific to funding organizations including formatting documents, figures and bibliography; assembling relevant supporting information including other support from faculty member and collaborators; formatting questionnaires, project manuals and codebooks. Code questionnaires received back. Maintains data base of all services provided and the key contact person compile and submit required reports to site coordinator from participants. Participate in endpoint review committee for a long term follow up study. Assist and implement elderly participant in research studies. Responsible for coordinating alumni meetings to inform study participant on analyzed data. Review annual questionnaires for new reports, data medical records, cause of illnesses, death certificates, procedures and medications. Generate weekly queries to ensure updated participant status. Create data bases according to requests and circulate to PI and other investigators for edits/approvals. Responsible for cleaning data files by combining data files and participating in the analysis of projects. Collaborates with the site PI, nursing staff and other partners affiliated with the grant. Create coding manual and address tables for questionnaire and test it before mailing. Maintain JHM IRB records and prepare all change in research and continuation submissions. Track intake and mailings of questionnaires or telephone request to administer phone interview. Regularly attends and actively participates in regularly scheduled meetingsJumokeResidential/Peer CounselorJuly 2014 December 2021Worked with DDA clients and provided each client with the necessary tools to be a productive member of society. Provide direct care and, in many cases, counseling or transportation. Monitor patients condition by observing physical and mental condition, intake and output, and exercise. Performed health assessments and screenings. Education on positive coping skills. Responsible for helping with activities of daily living, or ADLs, such as tooth brushing, showering and cooking, and arranging and transporting residents to appointments. Organize and oversee recreational activities. Conduct life skills and provide a safe and secure environment for the client. Escort clients to school, court appearances, probation officer visits and doctor appointments. Assist in the everyday functioning of all relevant office work such as generating correspondence, filing, research, collecting data as well as donation letters. Meet with the families of clients with the goal of uniting families. Facilitate and conduct group chats and recreational exercises. Interact with clients and their families as a family peer support worker. Meet with social workers, lawyers and other relevant staff in regards to the clients overall welfare Ensure that childrens serious issues are brought to the attention of the site manger Maintains data base of all services provided and the key contact person compile and submit required reports to site coordinator.Johns Hopkins University, Department of RheumatologyResearch CoordinatorSep 2008 Feb 2018As the Research Coordinator for the Department of Rheumatology, I served an important and highly public role. My position require that I am progressive and proficient in a high paced environment to help manage a team comprised of multi-levels of management and activities with physicians, research subjects and medical staff to help correlate hospital procedures with the research studies. Primary duties consist of, but are not limited to the following: coordinating studies; developing study flyers and other recruitment materials; interacting with clinicians and other gatekeepers to access patient populations; recruiting and scheduling research participants; conducting clinical testing such as, EKGs, phlebotomy and processing study recruits blood samples; collecting and recording data; establishing and maintaining paper files and computerized databases such as the Clinical Management System (CRMS) and Corona Database; conducting library/literature searches; participating in weekly research group meetings; monitoring and maintaining supply of research materials and order as needed; meeting regularly with Principal Investigator to review data accuracy and overall study progress; assisting in preparation and management of audits required by EIRb. In addition, this position requires that I evaluate collected study data; maintain required records of study activities including case report forms, drug dispensation records, or regulatory forms; communicate with laboratories or investigators regarding laboratory findings; and order drugs or devices necessary for study completion. Regularly track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts; Responsible for identifying protocol problems, informing investigators of problems, or assisting in problem resolution efforts such as protocol revisions.WORK HISTORYJohns Hopkins University, School of MedicinePatient Service CoordinatorApr 2001 Sep 2008Advanced RadiologyPatient Service CoordinatorOct 2004 Apr 2008Johns Hopkins UniversityResearch AssistantJan 2001-Oct 2004COMPUTER/TECHNICAL SKILLSMicrosoft Office Suite: Microsoft Word, PowerPoint & Excel, Teams, Epic, RedCap, ETO,EDUCATION/CERTIFICATESHigh School Diploma, Lawrence Central High School, 1997CERTIFICIATES OF TRAINING:Blood borne Pathogens, CACFP, CITI, Clinical, ClinPhone, (CRMS) Research Management System (CRMS), Covance, CPR, DDA, DrugDev, EKG, ERT, End point, Investigator Space, Medidata, Medtech, MSDE, Phlebotomy, PPD Preclarus, Teva, Signant IVRS Spaulding, Spirometry, YPrime |
