Cecile Lowe Email & Phone Number
Who is Cecile Lowe? Overview
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Cecile Lowe is listed as Retired Professional at RICE Designs, based in Metro Jacksonville, United States. AeroLeads shows a matched LinkedIn profile for Cecile Lowe.
Cecile Lowe previously worked as Retired at Rice Designs and Database Manager at Rice Designs. Cecile Lowe holds Health Information Management, 3.0 from Pgcc.
About Cecile Lowe
Cecile Lowe is a Retired Professional at RICE Designs. She possess expertise in analysis, research, software documentation, clinical research, nonprofits and 24 more skills. Colleagues describe her as "Cecile is both a detailed oriented manager and person." and "Sir/Ma'am: I am writing this recommendation with the pleasure to provide the highest recommendation for Cecile Lowe. I worked with her at Defense and Veterans Brain Injury Center (DVBIC) both at Walter Reed Army Medical Center and our headquarters in Rockville, MD. Cecile possesses a very high level of competence and professionalism. She effectively managed multiple complex projects simultaneously in addition to supervise her staff effortlessly. She was a pleasure to work with on a personal level; she was an excellent team player and was always ready to assist her coworkers with any tasks. Having such a warm personality with her professional expertise is hard to find in an employee. Cecile would be an excellent addition to your organization and I am honored to have worked with her. If you need additional information, free to contact me at 240-687-0659. Regards, Sherray Holland, PA-C"
Listed skills include Analysis, Research, Software Documentation, Clinical Research, and 25 others.
Cecile Lowe's current company
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Cecile Lowe work experience
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Database Manager
Database Manager• Maintains database results by setting and enforcing standards and controls.• Prepares for database expansion by studying plans and requirements.• Keeps senior technical management informed by preparing reports on system performance and problems.• Upgrades hardware and software by assessing transaction processing and database production options.• Maintains database performance by troubleshooting problems.• Secures database by developing policies, procedures, and controls.• Updates job knowledge by participating in educational opportunities, reading professional publications, and maintaining personal networks.
Clinical Data Abstractor
Tempoarary Position• Analyze and abstract medical data related to eye injuries and diseases from electronic computable and non-computable and hard copy medical records from various Department of Defense (DoD) and Veterans Affairs (VA) data sources. Enter abstracted data into the Defense and Veterans Eye Injury Vision Registry (DVEIVR) and the Veterans Affairs Eye Injury Data Store (VAIEDS) based on business rules, procedural requirements and individual judgment in applying those requirements.• Perform self-audits and peer reviews for regulatory compliance and verification of complete and accurate data abstraction based on medical and clinical understanding and judgment.• Collaborate with Clinical Staff Supervisor and Data Abstraction team in resolving issues and concerns identified.• Provide recommended corrective actions for data abstraction. Identify and document possible suggestions for improving the data abstraction process.• Work with Clinical Staff Supervisor and team to ensure clinical data integrity, to share findings, and coordinate corrective actions as necessary. Collaborate with team in resolving issues and concerns identified.• Analyze content of source documents (e.g., medical records, information systems) and abstract data considered appropriate for submission.• Ensure the complete and accurate abstraction, capture, and entry of patient information into the DVEIR and VAEIDS at a 98% or higher accuracy rate.• Manage submissions to the DVEIVR and VAEIDS based on knowledge and understanding of project requirements.• Validate and reconcile data from multiple sources as required.
Research Data Manager
Extensive data entry into CPDR multi-center national database, to include retrospective and prospective data collection. Sources of patient information will include handwritten, scanned or printed clinical forms to be maintained and kept secure in patient medical research charts. Performs systematic quality control and assurance measures per SOP to identify and reconcile data discrepancies with the guidance of clinical staff. Obtains Informed Consent from research subjects as permitted by site Institutional Review Board (IRB). Obtains missing data by interacting with clinical personnel, reviewing patient medical charts and/or electronic clinical databases, and patient follow-up. Responsible for safe and IRB-compliant handling of medical information and patient consent per guidelines set forth in CPDR's master research protocol. Interacts and maintains professional demeanor with members of CPDR scientific support branch, management staff, and others. Organizes and maintains patient research files according to CPDR's SOP. Generates QA/QC reports, prepares data query requests, assists with IRB protocol development and submission according to established procedures and guidelines. Establishes, evaluates and revises data collection processes to improve efforts of data collection at local site. Creates treatment-specific protocol packets for patients diagnosed with prostate cancer.. Provides assistance and training to the data entry personnel when new protocols begin or as new interface screens are added or modified. General administration/clerical duties such as research chart filing. Completes other duties as assigned.
Supervisor - Data Management (Wramc/Dvbic)
Supervise and provide database management support in the Department of Informatics for the Defense and Veterans Brain Injury Center (DVBIC) site research team, its staff with clinical research and related activitiesAssists clinical users in database interaction as necessary, performing queries when necessary for clinical and research staffSupervise the activities of data entry in the Data Group division of InformaticsEnsure all trial documentation are complete and complies with research protocol and guidelinesDevelop and manage mechanisms and protocols for sharing data with cooperating researchers and projectsPlans, assigns, and coordinate efforts to ensure a smooth flow of work within the divisionPrepares production schedulesMaintains records of attendance and productionTrains new operators in the use of software and database proceduresMaintains data entry on datasets on special or difficult projectsAttends meetings; develops new work methods and procedures
Cecile Lowe education
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Pgcc
Frequently asked questions about Cecile Lowe
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What company does Cecile Lowe work for?
Cecile Lowe works for RICE Designs.
What is Cecile Lowe's role at RICE Designs?
Cecile Lowe is listed as Retired Professional at RICE Designs.
Where is Cecile Lowe based?
Cecile Lowe is based in Metro Jacksonville, United States while working with RICE Designs.
What companies has Cecile Lowe worked for?
Cecile Lowe has worked for Rice Designs, Harris It Services, Center Of Prostate Disease Research (Cpdr), and The Henry Jackson Foundation.
How can I contact Cecile Lowe?
You can use AeroLeads to view verified contact signals for Cecile Lowe at RICE Designs, including work email, phone, and LinkedIn data when available.
What schools did Cecile Lowe attend?
Cecile Lowe holds Health Information Management, 3.0 from Pgcc.
What skills is Cecile Lowe known for?
Cecile Lowe is listed with skills including Analysis, Research, Software Documentation, Clinical Research, Nonprofits, Microsoft Office, Microsoft Word, and Management.
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