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Work Background
Clinical Data Manager
EDETEK (Awwcor. Inc)Clinical Data Manager
Aug. 2024Argentina• Support Internal Clinical Data Management Initiatives • Complete Traditional and Assigned Data Management Operations/Activities • Contribute to Project Success by Conducting Duties per CPM/LSCDM Request • Design Case Report Forms (CRFs), Code Data per Selected Coding Dictionaries, and Clean Data. Assist in the Development and Maintenance of Systems Used to Support Project Infrastructure • Work with Clinical Data Specialists (CDSs) to Execute Data Management Plans and with Clients/Sponsors as Necessary to Deliver Contracted Clinical Data Management Services and Clinical Data with High Quality and Integrity • Develop / Execute Testing Strategies and Assist with Data Transfers, Loading, and Integration. Complete All Required Documentation by EDETEK and Project Requirements • Perform Use Acceptance Testing (UAT) on New Software and Classify Clinical Events per Agreed-upon Strategies/Plans Classification. • BU Lead CDM • Project management duties
Laboratory Project Services Coordinator
Q² SolutionsLaboratory Project Services Coordinator
Jun. 2023 - Aug. 2024• Support the Project by assisting in Study initiation procedures and performing tasks associated with its day-to-day operation. • Maintain effective systems for project documentation. Provide Study Activity Monitoring and Closeout. • Ensure outputs are delivered in line with organizational standards, protocol-specific requirements, and Customer expectations. Participate in external and internal meetings. • Provide feedback to internal and external teams on the performance of Investigator sites and company services. Coordinate and communicate with relevant stakeholders, including leading Customer communications and activities. • Provide back-up to the Project Manager during the Project Manager's absence from the office.
Clinical Research Coordinator
Swiss Medical GroupClinical Research Coordinator
May. 2022 - May. 2023• Provide technical and administrative support to the principal investigator. • Collect and maintain investigation and site documents (Master Files). • Preparation of monitoring activities, audits, and inspections; electronic upload of study data; response to inquiries; training and adherence to the protocol, ICH-GCP, and local regulations. • Start-up tasks: preparing all the necessary documentation for the study. • Constantly communicate with regulatory agencies, ethics committees, suppliers, and CRO.
Surgical technician Coordinator
StrykerSurgical technician Coordinator
Aug. 2021 - Jan. 2022• Responsible for coordinating and managing surgeries with surgical technicians, kit room, and logistics teams. KPI and CAPA management • Lead, analyze, and control the services provided. Ensure that scheduled surgeries are adequately attended.
Depuy Synthes Loan control and Replenishment
Johnson & JohnsonDepuy Synthes Loan control and Replenishment
Mar. 2019 - Dec. 2020• Orthopedic and Medical Devices. Loan control, reconditioning, and replacement • Management of the peripheral warehouse
Instrumentadora Quirurgica
Sanatorio Sagrado CorazonInstrumentadora Quirurgica
Mar. 2017 - Jul. 2019• Delivered assistance and support to surgeons during general, gynecological, orthopedic, neurological, and plastic surgery procedures.
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