Mariruth Ross Larsen
In my most recent role as a TMF QC Manager at Novartis, I was responsible for ensuring the... | East Hanover, New Jersey, United States
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Mariruth Ross Larsen’s Emails ma****@no****.com
Mariruth Ross Larsen’s Phone Numbers 1212830****
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Mariruth Ross Larsen’s Location East Hanover, New Jersey, United States
Mariruth Ross Larsen’s Expertise In my most recent role as a TMF QC Manager at Novartis, I was responsible for ensuring the quality and compliance of the Trial Master File (TMF) for multiple clinical trials across different therapeutic areas. I have over 18 years of experience in clinical trial management, data management, and planning and tracking database functionality. I have developed and implemented effective TMF quality control processes, tools, and training mechanisms to support the clinical trial teams, the clinical research organizations, and the contract agencies. I have also contributed to the optimization and maintenance of the Clinical Trial Management System (CTMS) data quality and accuracy. I am passionate about facilitating better communication and collaboration among the stakeholders and improving the efficiency and performance of the clinical trials. I am CPR certified and have a strong knowledge of Good Clinical Practice (GCP) and clinical development.
Mariruth Ross Larsen’s Current Industry Novartis
Mariruth
Ross Larsen’s Prior Industry
Novartis
|
Novartis Pharmaceuticals
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Work Experience
Novartis
Trial Master File Quality Manager
Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis
Clinical Trial Management System Functional Manager
Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jan 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis Pharmaceuticals
Sr. Planner Of Clinical Operations
Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis Pharmaceuticals
Sr. Clinical Manager
Sun Jan 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis
Tmf Quality Control Manager
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FAQ About Mariruth Ross Larsen
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Mariruth Ross Larsen is located at
East Hanover, New Jersey, United States -
Mariruth Ross Larsen is a
In my most recent role as a TMF QC Manager at Novartis, I was responsible for ensuring the quality and compliance of the Trial Master File (TMF) for multiple clinical trials across different therapeutic areas. I have over 18 years of experience in clinical trial management, data management, and planning and tracking database functionality. I have developed and implemented effective TMF quality control processes, tools, and training mechanisms to support the clinical trial teams, the clinical research organizations, and the contract agencies. I have also contributed to the optimization and maintenance of the Clinical Trial Management System (CTMS) data quality and accuracy. I am passionate about facilitating better communication and collaboration among the stakeholders and improving the efficiency and performance of the clinical trials. I am CPR certified and have a strong knowledge of Good Clinical Practice (GCP) and clinical development. Novartis -
Mariruth Ross Larsen currently works in the
Novartis -
Mariruth Ross Larsen specializes in
In my most recent role as a TMF QC Manager at Novartis, I was responsible for ensuring the quality and compliance of the Trial Master File (TMF) for multiple clinical trials across different therapeutic areas. I have over 18 years of experience in clinical trial management, data management, and planning and tracking database functionality. I have developed and implemented effective TMF quality control processes, tools, and training mechanisms to support the clinical trial teams, the clinical research organizations, and the contract agencies. I have also contributed to the optimization and maintenance of the Clinical Trial Management System (CTMS) data quality and accuracy. I am passionate about facilitating better communication and collaboration among the stakeholders and improving the efficiency and performance of the clinical trials. I am CPR certified and have a strong knowledge of Good Clinical Practice (GCP) and clinical development. -
Mariruth Ross Larsen speaks the following languages:
No languages available. -
Mariruth Ross Larsen has prior experience in the following industries:
Novartis , Novartis , Novartis Pharmaceuticals , Novartis Pharmaceuticals -
Mariruth Ross Larsen has the following professional experience:
Novartis , Novartis , Novartis Pharmaceuticals , Novartis Pharmaceuticals , Novartis . -
You can view Mariruth Ross Larsen’s
LinkedIn profile at LinkedIn URL. -
Mariruth Ross Larsen’s work email addresses are
[email protected] . -
Mariruth Ross Larsen works at
Novartis
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