This curriculum vitae is for Valerie Watson, who has over 15 years of experience in clinical research coordination and administration. She is currently a Clinical Research Coordinator at Danbury Hospital, where her responsibilities include patient recruitment, protocol implementation, data collection, and ensuring regulatory compliance. Previously, she held roles as an Administrative Assistant/Clinical Research Coordinator and Medical Assistant/Secretary. Valerie has a Bachelor's degree in Biology from Western Connecticut State University and maintains several professional certifications. She has extensive training in good clinical practice and regulatory guidelines.
I am writing in regards to the Clinical Research Associate position that is open with your company at this time. I am an experienced CRA with over three years in clinical trials with broad background in clinical trials management of Phase II/III trials in various indications including the implementation of study protocols, monitoring of study sites and on-site data management and collection of study-related documents. With excellent organizational skills and a profound background of working in a managerial capacity, along with my ability to learn rapidly and proficiently, will allow me to be a valuable part of your team as well as contribute to your constant success.
What is the difference between development and adaptation of clinical practice guidelines? This was presented by Dr. Yasser Amer during the 2nd Regional Workshop for CPG adaptation, Tunis, Tunisia May 24-26 2016
Link:
https://www.facebook.com/media/set/?set=a.481589005298936.1073741852.215244758600030&type=1&l=67dff997c7
I am writing in regards to the Clinical Research Associate position that is open with your company at this time. I am an experienced CRA with over three years in clinical trials with broad background in clinical trials management of Phase II/III trials in various indications including the implementation of study protocols, monitoring of study sites and on-site data management and collection of study-related documents. With excellent organizational skills and a profound background of working in a managerial capacity, along with my ability to learn rapidly and proficiently, will allow me to be a valuable part of your team as well as contribute to your constant success.
What is the difference between development and adaptation of clinical practice guidelines? This was presented by Dr. Yasser Amer during the 2nd Regional Workshop for CPG adaptation, Tunis, Tunisia May 24-26 2016
Link:
https://www.facebook.com/media/set/?set=a.481589005298936.1073741852.215244758600030&type=1&l=67dff997c7
Alexandria Pediatric Center - Scientific Meeting Series 2017 - Meeting No. (7) conducted by Dr. Yasser Sami Amer
on 22nd August 2017 in Alexandria, Egypt
Illustration on how the CPGs Adaptation Program has helped in quality improvement through compliance with national and international accreditation standards.
Overview of Evidence-Based Practice Guidelines Initiatives in the Hospitals of Two Universities in the Middle East and North Africa Countries: Alexandria University Faculty of Medicine and University Hospitals and King Saud University College of Medicine and Medical City
Part 1. An overview on implementation of CPGs
Part 2. CPGs & HTAs
Presented during the 2nd Regional Workshop for CPG Adaptation, Tunis, Tunisia May 24-26 2016
A collaborative between INA Sante, WHO-EMRO, KSU
An introduction on Evidence-Based Clinical Practice Guidelines in Health Care Organizations
Brief on Alexandria Center for EBCPGs in Alexandria University Hospitals, Egypt
By Dr. Yasser Sami Abdel Dayem Amer, MBBCh, MS 2013
Special Thanks to
Prof Dr Mahmoud Elzalabany
Prof Dr Tarek Omar
Prof Dr Nabil Dowidar
Prof Dr Afaf Gaber
This session was conducted as a part of the 6th Resident Professional Development Course titled "Evidence-Based Medicine" in 9th SEPT 2015 at College of Medicine, King Saud University
Alexandria Pediatric Center - Scientific Meeting Series 2017 - Meeting No. (7) conducted by Dr. Yasser Sami Amer
on 22nd August 2017 in Alexandria, Egypt
Illustration on how the CPGs Adaptation Program has helped in quality improvement through compliance with national and international accreditation standards.
Overview of Evidence-Based Practice Guidelines Initiatives in the Hospitals of Two Universities in the Middle East and North Africa Countries: Alexandria University Faculty of Medicine and University Hospitals and King Saud University College of Medicine and Medical City
Part 1. An overview on implementation of CPGs
Part 2. CPGs & HTAs
Presented during the 2nd Regional Workshop for CPG Adaptation, Tunis, Tunisia May 24-26 2016
A collaborative between INA Sante, WHO-EMRO, KSU
An introduction on Evidence-Based Clinical Practice Guidelines in Health Care Organizations
Brief on Alexandria Center for EBCPGs in Alexandria University Hospitals, Egypt
By Dr. Yasser Sami Abdel Dayem Amer, MBBCh, MS 2013
Special Thanks to
Prof Dr Mahmoud Elzalabany
Prof Dr Tarek Omar
Prof Dr Nabil Dowidar
Prof Dr Afaf Gaber
This session was conducted as a part of the 6th Resident Professional Development Course titled "Evidence-Based Medicine" in 9th SEPT 2015 at College of Medicine, King Saud University
I have recently relocated to the Denver, Colorado area and I am actively seeking a position, in research, that can challenge and utilize the professional knowledge I have acquired over the past four years. I am a self motivated, ambitious young professional who has worked very hard to become an effective asset and team member to each organization which I have been a part of. Since my graduation with a BS Clinical Research, I have worked in a variety of positions including corporate CRO research (INC Research), direct clinical care (Nursing Assistant at UNC and Duke Hospitals), and most recently, Clinical Research on the site level with the Duke University Cardiothoracic Surgery Research Team. My previous team lead and research practice manager, included as references on my resume, will likely cite my ability and willingness to learn quickly, interact with subjects/patients in a personable manner, and develop productive working relationships with my team members. I pride myself on my work ethic and enjoy working around others that inspire that same dedication.
I have recently relocated to the Denver, Colorado area and I am actively seeking a position, in research, that can challenge and utilize the professional knowledge I have acquired over the past four years. I am a self motivated, ambitious young professional who has worked very hard to become an effective asset and team member to each organization which I have been a part of. Since my graduation with a BS Clinical Research, I have worked in a variety of positions including corporate CRO research (INC Research), direct clinical care (Nursing Assistant at UNC and Duke Hospitals), and most recently, Clinical Research on the site level with the Duke University Cardiothoracic Surgery Research Team. My previous team lead and research practice manager, included as references on my resume, will likely cite my ability and willingness to learn quickly, interact with subjects/patients in a personable manner, and develop productive working relationships with my team members. I pride myself on my work ethic and enjoy working around others that inspire that same dedication.
1. Valerie Watson, Curriculum vitae
Curriculumvitaeof: Valerie Watson, CCRC
205 Copper Square Drive, Bethel, CT 06801
vwatson2410@gmail.com
(203)994-4962 (mobile)
QUALIFICATIONS:
Highly-focused, with a strict attention todetailand accuracy.
Multi-tasking combinedwith excellent project managementskills and the ability to workwithin strict
deadlines.
Outstanding interpersonal skills, building positive relationships withstudy participants and sponsors.
Strong advocate of teamwork, performance excellence andcontinuous improvement.
EXPERIENCE
2011-Present DANBURY HOSPITAL, DEPARTMENT OFMEDICAL EDUCATION AND RESEARCH Danbury, CT
Clinical Research Coordinator
Responsible for theoverall coordination, organization, communication andefficientimplementation of
clinical trials.
Responsible for patient recruitment, coordination of care of the researchpatients, protocol
implementation, data collection and query resolution.
Responsible for screeningpatients for study participationby reviewing medicalrecord, collaborating with
medical and researchstaff as necessary.
Assists withobtaining and documenting informed consentaccording to standardoperating procedures.
Maintains accurate and through documentation onallsource documents and casereport forms for each
study patient, resolvingall patient queries.
Coordinates andparticipates in monitoring visits/audits with regulatory agencies and sponsors.
Participates in investigator, coordinator or study initiation meetings as required.
Responsible for educatingthe hospitalstaff about protocols throughin-services, written materials and
one-on-one interaction, for each studypatient and for generalmarketing.
Demonstrates flexibility in daily routineand effectively accommodates the needs of the job(i.e.:
late/early patient enrollment)
Participates in investigator, coordinator or study initiation meetings as required.
Responsible for regulatory documentpreparation for new andexistingIRBsubmissions.
Responsible for all adverse event reporting and proper documentation.
Responsible for conducting subject visits in accordance with sponsor protocolandGCP/ICHguidelines.
Responsible for preparingrecruitment plans and advertisement materials for sponsors.
Responsible for investigationalproduct accountability includingreceiving investigationalproductfrom
sponsor/CRO, providing appropriatestorage of products andsupplies according toICHguidelines,
ensuring the proper dispensingof the IP, ordering and returningused and unusedIP.
Assists in the account management of researchfunds, including paymenttracking from the sponsor to the
institution and payments topatients.
Responsible for organizing, planning, and presenting quarterly patient educationsessions.
Assists in training and development of new employees within the researchdepartment.
2008-2011 DANBURY OFFICEOF PHYSICIANSERVICES, PC, PULMONARY DEPARTMENT Danbury, CT
AdministrativeAssistant/Clinical Research Coordinator
Coordinated protocol implementation, obtaininganddocumentinginformed consent, IRBreporting,
query resolution, clinical data collection, reimbursement, serious adverse event reporting and retentionfor
clinical trials.
Assisted with budget development and maintenance.
Assisted with implementation of new policies and directives in accordance with organizationalguidelines
Extrapolated and prepared data for monitoring andquality assurancepurposes.
Decreased office expenditures byimplementingneeded controls on medicaland surgicalsupply stock,
office supplies andstandardizing ordering procedures.
2. Valerie Watson, Curriculum vitae
Assisted with development and implementationof new electronic medicalrecord and pharmacy
management system.
Provided training and supportfor department and network staff through electronic system transitions.
2005-2008 Scheduler/Secretary Danbury, CT
Answered phones, triagedcalls andtook messages, scheduled patientappointments, outpatient
procedures and testing.
Created daily assignment log for accountability and toensurethat allsecretarialtasks were completed in a
timely manner
Obtained, verified, and updated allinsurance informationto ensure proper andefficientregistration at
patient arrival
Obtained medical transcriptionfromphysicians to ensure promptprocessing byfile staff.
Functioned as a medical assistant and receptionistwhenstaffing needs demanded.
Created and implemented training guides, and competencyevaluations for new secretarialand file room
staff.
Assisted with clinical trial visits and data entry.
2001-2005 Medical Assistant/Secretary Danbury, CT
Demonstrated proficiencies in taking patientmedicalhistories, ROS, andvitalsigns as wellas performing
veinpunctures, EKGs, Simple Pulmonary Exercise Tests and medication teaching.
Ensured the cleanliness, sanitation, andmaintenance of allfacilities, exam rooms and equipment.
Developed efficiency-enhancingworkflow/process improvements thatmade it possible toaccommodate
increasing responsibilities necessitated byincreasing provider productivity.
Developed a safetystepfor bariatric patients toeliminate the exam room table hazardandtoincrease
accessibility.
Efficiently handled administrative duties toensurethat providers could focus onpatient satisfaction and
increase productivity.
Created and implemented training guides, and competencyevaluations for new medicalassistants to
ensure that consistency was achieved when trainingnew staff members.
PROFESSIONAL MEMBERSHIPS
Association of Clinical ResearchProfessionals (ACRP) – certified clinicalresearch coordinator – Active
Model Agreements & Guidelines International (MAGI) – Active
Society of Clinical Research Associates, Inc. (SoCRA) – Active
Society for Clinical Research Sites (SCRS) - Active
SKILLS AND ACTIVITIES
2008 – AttendedGCP/ICHseminar providedby Genentech for the EXCELS study.
2008 – AttendedDiversity in the Workplace Training provided byDanbury Hospital.
2008 – AttendedManager/Supervisor training provided by DanburyHospital.
2010 – AttendedICH/GCP trainingprovided byBoehringer Ingelheim.
2011 – NIHWeb-basedtraining course “Protecting Human ResearchParticipants.”
2011 – MAYO Medical Laboratories –“Handling/Offering for Transportation of Dangerous Goods.”
2011 - Attended ICH/GCP training provided by Boehringer Ingelheim.
2011 – AttendedICH/GCP trainingprovided byNovartis Pharmaceuticals.
2012 – ACRP CertifiedClinical Research Coordinator Exam –Passed
2012- Attended IATATraining provided by the State of Connecticut.
2012 - Attended ICH/GCP training provided by Boehringer Ingelheim.
2013 – AttendedICH/GCP “transcelerate” training providedby Boehringer Ingelheim.
2013 – AttendedICH/GCP trainingprovided byPearlTherapeutics.
2013 – NIHWeb-basedtraining course renewal“ProtectingHuman Research Participants.”
2013 – BLS for the Healthcare Provider provided by the American HeartAssociation
2014 – AttendedIATArenewal trainingprovided bytheState of Connecticut.
2014 – AttendedICH/GCP trainingprovided byAradigm.
2014 – Medidata certified professional
3. Valerie Watson, Curriculum vitae
2015 – AttendedICH/GCP trainingprovided byGlaxoSmithKline
2015 – BLS for the Healthcare Provider course renewalprovidedby the American HeartAssociation
EDUCATION
May 2010 WESTERN CONNECTICUT STATE UNIVERSITY Danbury, CT
B.A. in Biology
Researchprojects: “EcologicalImpactof Exotic Earthworm Introduction to NortheasternHardwood
Forests”and analysis of sedimentmetagenome community within Lake Zoar.
Metagenome analysis of soilsedimentfromLake Zoar was presentedat WestConn Research Day, May
14, 2010.
Elective courseworkin; Immunology, Microbiology, Molecular Genetics, Cell& Developmental
Biology, Anatomy and Physiology, andMedicinalChemistry.