Richard Willoughby has over 15 years of experience in the pharmaceutical and healthcare industries. He has worked as a Safety Data Analyst, Clinical Data Management Associate, and Information Specialist. He possesses skills in data management, pharmacovigilance, medical terminology, and working with databases such as ARISg, Oracle Clinical, and EDC.
Here is the slideset I presented at the 2nd International Conference on Business Analytic and Intelligence (ICBAI). The intent behind the paper/presentation was to bring out awareness on AE analysis and present status of AE data in india. Certainly there are huge potential benefit/insights out of this data if the base is set well. Private health care institutions can reap the benefit (Both financial and patient care) if they invest to define the system for their use.
Doctors generally provide hand written prescriptions to their patients. Sometimes it is difficult to understand name of the medicine(s) from the prescriptions. Hand written prescriptions do not also allow storing patients’ history and trend of patients. Hospitals/Clinics may want to preserve patients’ data or monitor prescriptions which are also not possible due to manual writing. All these disadvantages can be overcome by using a software application to save patients’ data and provide a printed prescription.
Here is the slideset I presented at the 2nd International Conference on Business Analytic and Intelligence (ICBAI). The intent behind the paper/presentation was to bring out awareness on AE analysis and present status of AE data in india. Certainly there are huge potential benefit/insights out of this data if the base is set well. Private health care institutions can reap the benefit (Both financial and patient care) if they invest to define the system for their use.
Doctors generally provide hand written prescriptions to their patients. Sometimes it is difficult to understand name of the medicine(s) from the prescriptions. Hand written prescriptions do not also allow storing patients’ history and trend of patients. Hospitals/Clinics may want to preserve patients’ data or monitor prescriptions which are also not possible due to manual writing. All these disadvantages can be overcome by using a software application to save patients’ data and provide a printed prescription.
Learn how to create and maintain a Trial Master File for your site or clinical trial and what are the critical components of a TMF. Register for the webinar.
Electronic Health Records: Implications for IMO State's Healthcare SystemMichael Loechel
Very high level overview and benefits of Electronic Health Records systems and a multi-phased approach to implementation. By Michael Loechel & Joy Gupta.
The Hospital is an Institute which provides to people best health services.
That Provides Facility for hospitalization.
The patient is admitted in hospital with the exception that he or she will be in the
hospital for more Than 24 hours.
The Patient is assigned a room /bed.
The Hospital Provide Medical care.
Talk at Heart Rhythm Society's 2013 annual Sessions discussing why and how patients will be able to obtain data from their implantable cardiac devices.
Learn how to create and maintain a Trial Master File for your site or clinical trial and what are the critical components of a TMF. Register for the webinar.
Electronic Health Records: Implications for IMO State's Healthcare SystemMichael Loechel
Very high level overview and benefits of Electronic Health Records systems and a multi-phased approach to implementation. By Michael Loechel & Joy Gupta.
The Hospital is an Institute which provides to people best health services.
That Provides Facility for hospitalization.
The patient is admitted in hospital with the exception that he or she will be in the
hospital for more Than 24 hours.
The Patient is assigned a room /bed.
The Hospital Provide Medical care.
Talk at Heart Rhythm Society's 2013 annual Sessions discussing why and how patients will be able to obtain data from their implantable cardiac devices.
DOLORES M. Stadtmauer
Ocala, Florida
SUMMARY OF QUALIFICATIONS
More than twenty years of experience various Including ten years of solid experience in the clinical drug development process Pharmaceutical and drug safety. Major Strengths: a solid work ethic, a mind for analytical detail, and an Ability to meet timelines in a challenging environment.
BUSINESS BACKGROUND
BRISTOL-MYERS SQUIBB COMPANY - HOPEWELL, NJ
Safety Regulatory Associate - Drug Safety & Pharmacovigilance GLOBAL & Labeling 04/99 - 10/05
• Responsible for identifying the comprehensive legal patient medical record in paper and electronic systems in Health Information.
• Duties include assuring all patient records and loose documents are scanned and indexed into the EPF with the highest level of quality possible.
• Responsible for full range of tasks performed in health information department with regard to health information management and maintenance.
• Provides customer service support of the health information department and any other duties assigned.
Challenges and Opportunities Around Integration of Clinical Trials DataCitiusTech
Conducting a Clinical Trial is a complex process, consisting of activities such as protocol preparation, site selection, approval of various authorities, meticulous collection and management of data, analysis and reporting of the data collected
Each activity is benefited from the development of point applications which ease the process of data collection, reporting and decision making. The recent advancements in mobile technologies and connectivity has enabled the generation and exchange of a lot more data than previously anticipated. However, the lack of interoperability and proper planning to leverage this data, still acts as a roadblock in allowing organizations truly harness their data assets. This document will help life sciences IT professionals and decision makers understand challenges and opportunities around clinical data integration
1. RICHARD MICHAEL WILLOUGHBY
7604 5th Ave upper
Kenosha, WI 53143
262-705-1549
auxaous@yahoo.com
SUMMARY: Hello, I am a business oriented professional with 15+ years in the
Pharmaceutical and Healthcare industry. I possess strong organizational and verbal
skills, analytical expertise, and interpersonal skills. I am detail oriented with an aptitude
for multi-task operations and have an ability to work independently with minimum
direction and/or within a group setting. Experience in the use of Arisg Safety databases,
and Oracle Clinical/EDC databases on many different clinical drug and medical device
studies, for many different companies/projects. I have experience in data management,
Pharmacovigilance and PV technology. Medical terminology is a strength. Hospital/ICU
experience. Experience working under strict deadlines.
SKILLS: Experience working in Global Safety/GPV, Adverse Event case processing and
narrative writing, ARISg, Oracle Clinical, EDC, RDC, IMedNet, AEGIS, MEDRA,
Windows/MS Office: Word, Excel, Outlook, Sharepoint. Oversaw/ran the scheduled
reporting area on the GPV team/data management team. Made assignments and
calendar, responsible for over 100+ reports (weekly, monthly, quarterly, etc). I helped
successfully lead the transition project of data management scheduled reporting area to
an outsourcing company.
Professional Job Experience
Baxter Healthcare Corporation 2013- Present
Deerfield, IL
Safety Data Analyst
Oversees/monitors outsourced scheduled reporting area in data management GPV
Generate complete and accurate periodic reports and ad-hoc reports
Standardize queries to ensure consistency ofreports generated
Collaborate with the report requester to assure accurate interpretation of the data request
Ensure timely completion and distribution of regulatory reports and query requests
Serve as a data integrity escalation contact for downstreamusers of Pharmacovigilance data (Safety
Writers, Medical Reviewers, Risk Management, Epidemiology, etc.)
Ensure consistent interpretation of systemrelated conventions,specifications,and definitions between
GIT and GPV functional areas
Ensure consistent interpretation of systemrelated conventions,specifications,and definitions between
GIT and GPV functional areas
Take initiative to recognize, prioritize & escalate potential safety/ compliance issues
Identify and troubleshoot root causes of thematic data integrity issues
2. RICHARD MICHAEL WILLOUGHBY
7604 5th Ave upper
Kenosha, WI 53143
262-705-1549
auxaous@yahoo.com
Identify potential errors and omitted data found during query and address them for review to the
responsible user
Participate in the development of system-related training programs in support of data integrity
initiatives
Other functions within Pharmacovigilance in all aspects ofdata management
Advanced Clinical Aug 2010-Mar 2013; Deerfield, IL
Clinical Data Management Associate
Follow Standard Operating Procedures (SOP’s), Data Processing Plans (DPP’s) and client conventions
to perform first and second pass entry
Perform DCF entry
Provide feedback using the error tracking systemand verbal/visual communication to personnel
performing entry
Perform QC checks using applicable browser tools
Aiding in Study Set-up (User Acceptance Testing on the database and on edit checks)
Assist with DM review (Manual review verifying edit checks in the DMRP are working properly.
Identifying data discrepancies outside of the DMRP and creating manual queries where necessary
Provide feedback and communicate potential issues to Clinical Data Managers (CDM’s) and Project
Leads on study-related discrepancies and issues
Review PageTrack reports for accuracy and consistency
Assist in the maintenance of the Data Management Plan (DMP)
Assist with Final QC Reviews and data listing audits
Assist the CDM or Senior CDM with maintaining/compiling all study documentation
Tracking and filing
Prepare CRFs for data entry (set-up)
Participate in client meetings when applicable
Assist in the creation and reviewing of SOPs and training manuals
Ad hoc report writing
Database Testing
Assist in training employees
Perform other duties as requested by management
3. RICHARD MICHAEL WILLOUGHBY
7604 5th Ave upper
Kenosha, WI 53143
262-705-1549
auxaous@yahoo.com
Senior Clinical Data Operator
Follow Standard Operating Procedures (SOP’s), Data Processing Plans (DPP’s) and client conventions
to perform first and second pass entry on CRFs
Inform Clinical Data Managers (CDMs) of any study-related discrepencies/issues including
feedback on the DMP for the study
Provide feedback using the error tracking systemand verbal/visual communication to personnel
performing entry
Use error reports as feedback to improve entry performance
Prepare CRFs for data entry (set-up)
Perform Data Clarification Form (DCF) entry (1st and 2nd pass)
Perform QC checks using the applicable browser tools
Learn how to utilize the DMRP
Create and enter test data for User Acceptance Testing on the database prior to activation and
provide feedback to the CDM
Assist with Final QC Reviews
Provide data entry training for new employees
Clinical Data Operator
Follow Standard Operating Procedures (SOP’s), Data Processing Plans (DPP’s) and client conventions
to perform first and second pass entry on CRFs
Inform Clinical Data Managers (CDMs) of any study-related discrepencies/issues including
feedback on the DMP for the study
Provide feedback using the error tracking systemand verbal/visual communication to personnel
performing entry
Use error reports as feedback to improve entry performance
Prepare CRFs for data entry (set-up)
Perform QC checks using the applicable browser tools
Learn how to utilize the DMRP
Manpower (Contracted to Abbott Laboratories) Aug 2008-May 2010 Waukegan, Il
Information Specialist II (Safety/Pharmacovigilance)
Proficiency in use of the AEGIS Database
Casing processing for AEs (adverse drug events (in both post-marketing and clinical settings)
Operation according to specific deadlines
Narrative and medical history writing , use of medical terminology, coding of drugs and medications
4. RICHARD MICHAEL WILLOUGHBY
7604 5th Ave upper
Kenosha, WI 53143
262-705-1549
auxaous@yahoo.com
Vista Health/Vista East Hospital Aug 1998-Aug 2008 Waukegan,IL
ICU Unit Secretary/Monitor Tech
Monitoring/reporting of patients life-signs/vitals in the Intensive Care Unit
Data entry and transcription of physicians /nurses orders
Providing support for daily operations in the ICU. Construction and maintenance of patient charts and
other medical records
Answering phones/Greeting visitors
Scheduling appointments, tests and transportation
Skills
ARISg, Oracle Clinical Database, EDC databases,Windows/MSOffice: Word, Excel, Outlook
Medical terminology background,familiar with disease/condition names, treatments, drug names, etc.
Experience working in Safety/GPV databases
Experience querying/discrepancy management on drug and medical device studies
Skills working understrict deadlines
Excellent auditing/QC skills
Adverse event case processing/narrative writing
Some medical coding experience
Creative writing and editing skills
Computer and data entry skills
Excellent coffee-making skills
Detail oriented/keen observationalskills
Education
University of Wisconsin-Parkside Kenosha,WI
Graduated 2004/BA English