
Pspm Support Associate
Há 2 dias
- up, maintenance and close out of Global or Regional projects, where delegated by the Global Safety lead of PSS Management team.
- Supports Global Safety lead in the preparation of pharmacovigilance reports for products and safety issues, including Individual Case Summary Reports (ICSRs) of Serious Adverse Events (SAEs), Annual IND reports, Development Safety Update Report (DSUR) Periodic Safety Reports (PSRs) line listings, and aggregate reports.
- Support Global Safety lead with reconciliation of safety databases, if appropriate.
- Support Global Safety Lead in drafting/modifying and delivering safety presentations as required, to external and internal stakeholders.
- Maintains a comprehensive understanding of Labcorp departmental Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance.
- Possess knowledge of other procedural documents, e.g. SOPs, etc. that impact department.
- Assist in the development of departmental Work Instructions (WI) and Standard Operating Procedures (SOPs), as appropriate.
- Ensure compliant safety reporting in accordance with US and international reporting regulations, SOPs and safety processing guidelines set forth by departmental management team and the client.
- Support the Global Safety lead in the generation of monthly status and other project-specific reports ensuring the quality and accuracy of metrics/data are provided.
- Build and maintain good departmental relationships across functional units.
- Support the Global Safety lead in preparation of Safety Management Plans (SMPs), Reconciliation Plans and other safety-specific plans under supervision.
- Support the Global Safety lead in preparation of study specific job aids, instructions, trainings and templates.
- Support systems set up during study start up and ongoing maintenance.
- Support the Global Safety lead project specific functional management for assigned projects (access requests, training assignment etc.)
- Assist in TMF management activities as required.
- To support the Global Safety lead in the preparation of internal, client or regulatory audits.
- Support the Global Safety Lead in the provision of data to Safety Committees/DSMBs.
- Demonstrate role-specific competencies on a consistent basis.
- Demonstrate company values on a consistent basis.
- Any other duties as assigned by Global safety lead or PSS management.
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Pspm Support Associate
Há 4 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroProvide support for the set - up, maintenance and close out of Global or Regional projects, where delegated by the Global Safety lead of PSS Management team. - Supports Global Safety lead in the preparation of pharmacovigilance reports for products and safety issues, including Individual Case Summary Reports (ICSRs) of Serious Adverse Events (SAEs), Annual...
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Clinical Research Professional
Há 4 dias
Cidade Jardim, Brasil beBeeClinical Tempo inteiro R$72.000 - R$98.000Job Title: Clinical Research Associate IJob Description:This position is responsible for providing clinical support to projects, adhering to Standard Operating Procedures (SOPs), ICH Guidelines and Good Clinical Practice (GCP).Responsibilities:To develop and/or maintain tracking systems for clinical projects.Responsible for all aspects of study site...
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Start-up Associate
Há 3 dias
Cidade Jardim, Brasil Labcorp Tempo inteiro**Main activities** - With support from a more experienced start up team member, works on low complexity studies (e.g., internal CRU or smaller external site studies in the EU and US, generally not Sponsor facing). - Primary contact and liaison with investigative sites during study maintenance and, when assigned, site start-up (SSU) activities. - Ensures all...
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Start-up Associate
3 semanas atrás
Cidade Jardim, Brasil Labcorp Tempo inteiro**Main activities**- With support from a more experienced start up team member, works on low complexity studies (e.g., internal CRU or smaller external site studies in the EU and US, generally not Sponsor facing).- Primary contact and liaison with investigative sites during study maintenance and, when assigned, site start-up (SSU) activities.- Ensures all...
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Assoc Medical Dir
Há 4 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroResponsible for medical review of serious adverse events and nonserious adverse events from clinical trials and postmarketing surveillance in support of drug safety activities for clients. - Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed to identify drug safety issues in collaboration with the...
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Clinical Research Team Member
1 semana atrás
Cidade Jardim, Brasil beBeeClinicalResearch Tempo inteiro R$86.400 - R$121.800Clinical Research Associate JobAre you a detail-oriented and organized professional seeking a challenging role in clinical research? Do you have excellent communication and problem-solving skills? We are looking for a Clinical Research Associate to join our team!The successful candidate will be responsible for monitoring and managing clinical trial sites,...
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Assoc Medical Dir
Há 3 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroResponsible for medical review of serious adverse events and nonserious adverse events from clinical trials and postmarketing surveillance in support of drug safety activities for clients.- Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed to identify drug safety issues in collaboration with the...
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Associate Project Manager, Start-up
Há 5 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroGENERAL - Lead start-up team during study start-up phase liaising directly with Lead SUPM or Project Lead, core team members and the client, as applicable. - Serve as client’s contact for start-up and maintenance processes and oversight. Responsible for establishing a strong working relationship with client’s project teams. - Monitor and control start up...
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Clin Res Assoc I
Há 5 dias
Cidade Jardim, Brasil Labcorp Tempo inteiroTo provide clinical support for projects according to Standard Operating Procedures, ICH Guidelines and GCP. - To develop and/or maintain tracking systems for clinical projects. - Responsible for all aspects of study site monitoring with or without direct supervision (as per the training status of the CRA I MEA). This includes remote and/or onsite conduct of...
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Start-up Professional
Há 2 dias
Cidade Jardim, Brasil beBeeCareer Tempo inteiro R$60.000 - R$90.000Job OverviewWe are seeking a highly skilled professional to join our team as a Start-up Associate. This role will involve working with experienced team members on low complexity studies, such as internal CRU or smaller external site studies in the EU and US.The successful candidate will be responsible for ensuring all assigned contractually related start-up...