Labcorp
Responsibilities / Duties: In this role you will be responsible for managing clinical projects to ensure the successful delivery of all lab services, including kits shipment, sample testing and sample management of a clinical study for the Asia region Act…
We believe in the power of partnership to fuel insights and unlock new possibilities. We offer our customers a tailored approach to clinical trial solutions through the use of three delivery models: full service, functional service providers, or a hybrid…
The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and…
The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and…
The Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans,…
Responsibilities / Duties: Act as regional liaison between Global Study Manager and various CCLS departments involved in the study. Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors) and the corresponding local CCLS platform; occasionally, the Regional…
Ready to reach your career goals in 2023?. We are seeking a Senior Clinical Research Associate I to join our clinical operations team that monitors Phase I IV clinical trials. Here, you\xe2\x80\x99ll have the opportunity to personally advance healthcare and…
Essential Job Duties: Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre study and initiation visits, with or without guidance (as per the training status of…
b' Essential Job Duties: Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre study and initiation visits, with or without guidance (as per the training status…
General Tasks Responsible for maintaining awareness of regulatory legislation, guidance and practice, ICH/GCP and relevant Sponsor requirements Take ownership in the preparation (collection, organization and compilation) of routine submissions filed to IRB/EC/Third body/Regulatory Authorities (e.g. INDs/CTAs) including but not limited…
b' General Tasks Responsible for maintaining awareness of regulatory legislation, guidance and practice, ICH/GCP and relevant Sponsor requirements Take ownership in the preparation (collection, organization and compilation) of routine submissions filed to IRB/EC/Third body/Regulatory Authorities (e.g. INDs/CTAs) including but not…
The Associate Start up Project Manager oversees and manages the start up phase of domestic and/or international clinical trials, primarily on a regional level but can hold a lead role depending upon SUPM experience level. Responsibilities include project managing defined…
The Associate Start up Project Manager oversees and manages the start up phase of domestic and/or international clinical trials, primarily on a regional level but can hold a lead role depending upon SUPM experience level. Responsibilities include project managing defined…
Responsibilities/Duties In this role you will be responsible for managing clinical projects to ensure the successful delivery of all lab services, including kits shipment, sample testing and sample management of a clinical study for the Asia region Act as regional…
Responsibilities/Duties In this role you will be responsible for managing clinical projects to ensure the successful delivery of all lab services, including kits shipment, sample testing and sample management of a clinical study for the Asia region Act as regional…
b' The Associate Start up Project Manager oversees and manages the start up phase of domestic and/or international clinical trials, primarily on a regional level but can hold a lead role depending upon SUPM experience level. Responsibilities include project managing…
Ready to reach your career goals in 2023 We are Labcorp, a leading global life sciences company, named by Fortune magazine\'s 2021 List of World\'s Most Admired Companies. Thanks to the more than 70,000 amazing employees around the globe who…
Ready to reach your career goals in 2023? We are Labcorp, a leading global life sciences company, named by Fortune magazine\'s 2021 List of World\xe2\x80\x99s Most Admired Companies. Thanks to the more than 70,000 amazing employees around the globe who…