
Regulatory Affairs Specialist
Há 4 dias
Job Description: The position will have primary responsibility in the Global Development Information Management team. A key responsibility of this role is to identify and recommend improvements to business processes, regulatory data, and data definitions for the RIM platform, while working in close collaboration with Global Regulatory Operations (GRO), Global Regulatory Affairs (GRA) and cross-functional stakeholders (e.g., IT, Clinical, Nonclinical, Quality). Identify opportunities within the RIM platform, to enhance compliance, efficiency, and reporting. Responsible for supporting RIM Reporting and Analytics needs across Global Regulatory Affairs as needed.Responsibility:Support efforts to align business processes to a RIM enterprise data strategy.Contribute to implementation of E2 E RIM which includes new system implementation, change requests, upgrades, integrations, data quality, metrics & reporting, etc.Ensure user's requirements are adequately documented and serve as the basis for system continuous improvement, process engineering/mapping, and/or new system selection.Conduct training and support change management activities in RIM implementation and upgrades.Track alignment of business processes and models across all business functions supporting global Regulatory product registrations.Lead and/or support initiatives to integrate Regulatory information and records globally and for acquired assets and products.Monitor emerging structured data standards or health agency requirements, assess business impact and define roadmap for addressing them.Required Skills and Experience: 6+ years of experience in working in a biotechnology or pharmaceutical Regulatory Affairs Operations environmentExperience in systems management or implementation in the life sciences industry or regulated industry.Must have experience in Veeva Vault RIMOther system experience preferred and may include Calyx, Lorenz, Integras, SPORIFY, and other Veeva Vaults (Promo Mat, e TMF, Quality)Microsoft Office and Adobe systems• Knowledge of regulations, processes and industry standards and best practices that govern regulated systems, records retention and Gx PCompensation: $15/hour - $25/hr USD
-
Regulatory Affairs Specialist
Há 4 dias
Ituiutaba, Brasil Insight Global Tempo inteiroJob Description: The position will have primary responsibility in the Global Development Information Management team.A key responsibility of this role is to identify and recommend improvements to business processes, regulatory data, and data definitions for the RIM platform, while working in close collaboration with Global Regulatory Operations (GRO), Global...
-
Business Compliance Strategist
Há 2 dias
Ituiutaba, Brasil Bebeecompliance Tempo inteiroRegulatory Affairs Specialist Job DescriptionThe Regulatory Affairs Specialist will play a pivotal role in enhancing compliance, efficiency, and reporting within our organization.This individual will work closely with cross-functional stakeholders to identify and recommend improvements to business processes, regulatory data, and data definitions for the RIM...
-
Senior Regulatory Specialist
Há 4 dias
Ituiutaba, Brasil Fortrea Tempo inteiroJob Overview:Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are made within the timelines agreed with project management and Site...
-
Safety Systems Analyst
2 semanas atrás
Ituiutaba, Brasil Bebeepharmacovigilance Tempo inteiroAs a liaison between business stakeholders, regulatory teams and IT professionals, the Adverse Event Reporting Specialist plays a crucial role in ensuring pharmacovigilance systems and workflows support accurate and compliant adverse event reporting.This position is critical in maintaining patient safety, regulatory compliance and efficient...
-
Veeva Specialist _ Veeva Clinical
2 semanas atrás
Ituiutaba, Brasil Hcltech Tempo inteiroInternational Opportunity for Veeva Specialist – Veeva Clinical / Limfinity / JMP Are you a professional ready to take your expertise global?HCLTech is hiring for a high-impact international project in Mexico City , and we're looking for talented individuals with experience in Veeva Clinical, Limfinity LIMS, and JMP .This is your opportunity to work at the...
-
Pharmacovigilance Business Analyst
1 semana atrás
Ituiutaba, Brasil Hyqoo Tempo inteiroTitle: Pharmacovigilance Business AnalystLocation: RemoteThe Pharmacovigilance Business Analyst (Pharma Cov BA) will serve as a key liaison between business users, regulatory teams, and IT, ensuring that pharmacovigilance systems and workflows support accurate and compliant adverse event reporting. This role is critical in maintaining patient safety,...
-
Pharmacovigilance Reporting Specialist
2 semanas atrás
Ituiutaba, Brasil Icon Plc Tempo inteiroPharmacovigilance Reporting Specialist - Brazil, Sao Paulo (Office Based - Hybrid)ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Pharmacovigilance...
-
Pharmacovigilance Business Analyst
2 semanas atrás
Ituiutaba, Brasil Hyqoo Tempo inteiroTitle: Pharmacovigilance Business Analyst Location: Remote The Pharmacovigilance Business Analyst (PharmaCov BA) will serve as a key liaison between business users, regulatory teams, and IT, ensuring that pharmacovigilance systems and workflows support accurate and compliant adverse event reporting.This role is critical in maintaining patient safety,...
-
Quality And Engineering Specialist
2 semanas atrás
Ituiutaba, Brasil Dtx Aerospace Tempo inteiroAbout us:DTX Aerospace is a leading company in the aerospace industry. Known for its innovative approach and cutting-edge technology, the company specializes in the design, manufacture, and maintenance of Landing Gears. With a strong focus on quality and safety, we have established ourselves as a trusted partner to many major airlines and military...
-
Clinical Nurse Specialist
2 semanas atrás
Ituiutaba, Brasil European Pharma Group Tempo inteiroLead the design and implementation of training and educational programs to support the adoption and sustained use of the Insujet TM System in [Country], in alignment with Sol-Millennium Medical Ltd's commercial strategy.Job ResponsibilitiesServe as the Clinical Product Specialist for the Insujet TM portfolio, delivering expert support to external...