Chief Risk Officer Jobs in Trenton
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Daiichi Sankyo, Inc.-Trenton
under guidance of CSL and/or Medical Monitor. Represents Clinical Development on Study Team and collaborates as team member with other functions, ARO, CRO. Provides scientific input to Clinical Operations and other functions. This position provides...
Daiichi Sankyo, Inc.-Trenton
with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations...
mindmatch.ai -
Daiichi Sankyo, Inc.-Trenton
statistical analyses. Additionally, this position interacts with study teams, as well as statisticians and programmers at CROs. This position works under some supervision to solve complex study problems.
Responsibilities
• Protocol Development, Case Report...
Daiichi Sankyo, Inc.-Trenton
with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations...
Daiichi Sankyo, Inc.-Trenton
specified product profile.
• CRO / Vendor Oversight: Review CRO/vendor proposal and budget. Establishes procedures through regular interaction, setting expectation on deliverables and timelines to guide CRO biostatistician and statistical programmers...
Daiichi Sankyo, Inc.-Trenton
tasks, including SDTM and collaborating with CROs and other vendors to ensure high quality deliverables to support drug development processes and global submissions as required for clinical trials. These include developing and validating SAS programs...
mindmatch.ai -
Daiichi Sankyo, Inc.-Trenton
consultants (i.e. CRO's) as needed.
Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.
Education Qualifications (from an accredited college or university)
• Bachelor's Degree...
Daiichi Sankyo, Inc.-Trenton
and programmers at CROs. This position works under some supervision to solve complex study problems.
Responsibilities
• Protocol Development, Case Report Form (CRF; review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation...
Daiichi Sankyo, Inc. | Associate Director, Clinical Study Startup, Clinical Safety and Pharmacovigil
Daiichi Sankyo, Inc.-Trenton
with CS Physicians and other study team members. This position will oversee and may engage within CSPV and with CROs to execute study start up processes. This level will handle problems requiring escalation from others and make decisions where appropriate...
mindmatch.ai -
Daiichi Sankyo, Inc.-Trenton
with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations...
Trenton
with in-house personnel, clinical sites and outside contractors/CROs.
• Develop and maintain professional relationships with key physicians, clinicians and principal investigators to assure good clinical input to Pacira Medical Device product development process...
pacira.com -
Daiichi Sankyo, Inc.-Trenton
Clinical Development, Research Development, Regulatory Affairs. Facilitate operational meetings with CROs, License Partners, and PV vendors. Provide PV oversight of the DSI Call Center. Provide oversight of ICSR processing activities including, Safety...
mindmatch.ai -
Daiichi Sankyo, Inc.-Trenton
Clinical Development, Research Development, Regulatory Affairs. Facilitate operational meetings with CROs, License Partners, and PV vendors. Provide PV oversight of the DSI Call Center. Provide oversight of ICSR processing activities including, Safety...
Daiichi Sankyo, Inc.-Trenton
programming tasks, including SDTM and collaborating with CROs and other vendors to ensure high quality deliverables to support drug development processes and global submissions as required for clinical trials. These include developing and validating SAS...
Daiichi Sankyo, Inc.-Trenton
with outside consultants (i.e. CRO’s) as needed.
Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.
Education Qualifications (from an accredited college or university)
• Bachelor's...
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