Chief Risk Officer Jobs in San Diego
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San Diego (CA)
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Search Results - Chief Risk Officer Jobs in San Diego
Katalyst Healthcares & Life Sciences-San Diego
Responsibilities:
Manage programming activities on project or study level, including managing CROs to ensure deliverables are accurate and compliant.
Act as a Programming SME for assigned studies, including authoring/reviewing programming...
resume-library.com -
Tr1X-San Diego
closely with study teams from vendors and CROs to achieve departmental and project goals. The Sr. CTA adheres to the Company's core values and complies with all applicable regulations, ICH-GCP guidelines, and SOPs. The Sr. CTA understands trial and study...
Katalyst Healthcares & Life Sciences-San Diego
including remote visits.
Experience in CRO/Vendor management (domestic/international) monitoring of budget scope.
Comprehensive knowledge of ICH, GCP, IRB/IEC, and local regulatory authority requirements.
Proficiency working with Microsoft Office Suite...
resume-library.com -
WuXi AppTec Group-San Diego
partners, academic collaborators, and partner CROs.
9. Work with the Business Development (BD) team to support marketing efforts, including the creation of materials, presentations, and client-facing documents to showcase the company's capabilities...
appcast.io -
Katalyst Healthcares & Life Sciences-San Diego
in scientific or health-related field.
Minimum of 9-11 years of clinical data management experience in the pharmaceutical and biotechnology industry or in a CRO.
At least 1 year experience working at a Sponsor.
Oncology trial experience required; hematology...
resume-library.com -
ADARx Pharmaceuticals Inc.-San Diego
tracking and oversight of clinical site budgets/payments in relation to conduct of a clinical trial.
• Manage IRB/IEC and regulatory submissions, as needed.
• CRO management and oversight.
• Establish vendor management plans and review quality metrics...
LanceSoft Inc-San Diego
and completion of Central Cell Bank requests
" Accurate and timely documentation and record keeping for audit and IND filing purposes.
" Weekly communication and updates with manager and CRO to ensure set goals are achieved and maintained.
" Work as part...
resume-library.com -
Association of Clinicians for the Underserved-San Diego
4. Drive indication selection and target market prioritization for drug development programs.
5. Foster relationships with principal investigators, clinical research organizations (CROs), regulatory bodies (FDA/EMA), and key stakeholders.
6. Act...
appcast.io -
Mindlance-San Diego
inventory and completion of Central Cell Bank requests
" Accurate and timely documentation and record keeping for audit and IND filing purposes.
" Weekly communication and updates with manager and CRO to ensure set goals are achieved and maintained...
resume-library.com -
Iambic Therapeutics, Inc-San Diego
/development goals.
• Oversee non-clinical ADME/PK and PK/PD studies, manage CRO and collaboration with external experts to supplement internal capabilities.
• Support regulatory submissions (INDs) by providing DMPK data, report and expertise.
• Stay...
Stage Solutions Inc-San Diego
management tools like JIRA and Confluence
• Demonstrated experience in managing external vendors and CROs for NGS or other research services
• Proficiency in molecular biology techniques, including DNA/RNA extraction & purification, NGS library preparation...
jobvertise.com -
ADARx Pharmaceuticals Inc.-San Diego
Outstanding Monitoring Reports) to ensure that the study is conducted per plan and communicates issues to Clinical Team Members as appropriate.
• Manage and oversee contracted CROs and vendors; identify potential risks and resolve issues with CROs; establish...
San Diego
of Biotech/Pharmaceutical/CRO working experience.
• Experience with managing teams and projects.
Knowledge / Skills / Abilities:
• Demonstrated broad expertise in immunology and cell biology.
• Expertise with cellular models, such as human PBMC and whole...
icims.com -
Codera-San Diego
bioanalytical labs and other contract research organizations (CROs)
Prepare, analyze and interpret PK data to produce reports that integrate into clinical and regulatory documents
Draft, edit and review sections of regulatory submissions and clinical documents...
Michael Page-San Diego
About Our Client
The client is a rapidly expanding global CDMO/CRO with multiple U.S. locations, specializing in API & Small Molecule development, Biologics, Cell & Gene Therapy, DMPK, Clinical Research, and Bioanalytical Sciences. They have built...
michaelpage.com -
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