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Chief Risk Officer Jobs in New Jersey

1 - 15 of 57
1 - 15 of 57
Search Results - Chief Risk Officer Jobs in New Jersey
BESTMSLs-Princeton (NJ)
activities of the contracted CRO, focusing on the CRA team. The CTLM also addresses unresolved investigator concerns, engages with PIs for study updates and recruitment plans, and supports local site staff and trial team members. Additionally, the role...
BESTMSLs-Princeton (NJ)
activities of the contracted CRO, focusing on the CRA team. The CTLM also addresses unresolved investigator concerns, engages with PIs for study updates and recruitment plans, and supports local site staff and trial team members. Additionally, the role...
mindmatch.ai -
Katalyst Healthcares & Life Sciences-East Windsor (NJ)
Responsibilities: Act as the point of contact for DM activities for the assigned clinical studies and proactively provide DM expertise to both internal and CRO cross-functional teams. Assist the head of data management in establishing standards...
resume-library.com -
Daiichi Sankyo, Inc.-Newark
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...
2 similar jobs: Jersey City, Trenton
Katalyst Healthcares & Life Sciences-South Plainfield
Responsibilities: Act as primary liaison between Company and CRO for Data Management. Provide support and oversight for the CRO Data Management team. Collaborate with the team on study design, protocol development, CRF design, statistical...
resume-library.com -
1 similar job: Cincinnati
Penns Grove
Agreement Specialist at ClinChoice (View all jobs) United States Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s...
pharmiweb.jobs -
Katalyst Healthcares & Life Sciences-South Plainfield
Responsibilities: Creation of SAS programs to Develop or Validate SDTM/ADaM/TLFs. Provide oversight for CRO SDTM/ADaM/TLFs deliverables for multiple studies and make sure efficiencies are gained at project level. Generate and/or review of SDTM...
resume-library.com -
Daiichi Sankyo, Inc.-Trenton
review of vendors agreements and policies, external training materials (e.g., CRO training materials), study protocols, subject recruitment materials, clinical study agreements, research collaboration agreements, informed consent forms or other...
2 similar jobs: Jersey City, Newark
Cost Management Incentives Inc-Princeton (NJ)
providers and other outsourcing needs. Responsibilities include clinical CRO/vendor identification, RFI/RFP development and execution, vendor selection, contract negotiations, budget management and service provider performance metrics development...
resume-library.com -
Daiichi Sankyo, Inc.-Newark
management and performance of CRO; Participates in creation of developmental and regulatory strategy; Drafts protocol profiles and sections of key submission documents; Point of contact for interactions with regulatory-agency clinical reviewing divisions...
2 similar jobs: Jersey City, Trenton
Katalyst Healthcares & Life Sciences-South Plainfield
in pharmaceutical or CRO environments. In-depth knowledge of CDISC SDTM, ADaM. Deep understanding of data dependencies, validation techniques. Thorough knowledge of SAS is required. Experience in R programming language and R Shiny app development is preferred...
resume-library.com -
Sanofi-Bridgewater (NJ)
initiatives.About youPhD/MS in statistics or related discipline with typically at least 8 years of pharmaceutical experience in clinical development, including experience with Biotech, pharma, Clinical Research Organizations (CROs), health authorities and academic...
Daiichi Sankyo, Inc.-Jersey City
and outside of Daiichi Sankyo (e.g. clinical trial sites, CROs, collaboration partners); Supports effective direct communication with clinical sites in collaboration with clinical development staff.  •  Consults with KEE's for advice on complex patient safety...
2 similar jobs: Trenton, Newark
ACADIA Pharmaceuticals Inc.-Princeton (NJ)
regulatory, commercial, and clinical development.  •  Lead efficient execution of the phase IV studies, including oversight of CROs, compliance with company’s policies and procedures, and study budget management.  •  Provide medical expertise and editorial...
appcast.io -
Princeton (NJ)
The CTLM represents the company in site relations, supports study teams with startup and recruitment, and manages in-field activities of the contracted CRO, focusing on the CRA team. The CTLM also addresses unresolved investigator concerns, engages with PIs...
icims.com -
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