Author Jobs in South San Francisco
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Search Results - Author Jobs in South San Francisco
AbbVie-South San Francisco
into research or development programs.
Description:
Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy.
Author regulatory documents including protocols, study reports, population PK...
resume-library.com -
Clinical Dynamix, Inc.-South San Francisco
monitoring strategy and oversight plan and ensure that the monitoring activities for each assigned study/region are compliant with the Clinical Monitoring Plan.
Author or review Clinical Monitoring Plan.
Participate in site feasibility, qualification...
jobvertise.com -
AbbVie-South San Francisco
and interpretation by providing necessary context (including explaining MoA and disease specifics, available relevant internal and external data, analysis plans, interpretation and discussion of model results in the context of research question).
Author regulatory...
resume-library.com -
South San Francisco
and/or batch records. Interpret and present experimental data to provide guidance for projects and process development.
• Author or review technical reports, technology transfer documents, SOPs, and invention disclosures.
• Plan and coordinate external...
tiptopjob.com -
AbbVie-South San Francisco
reports
Author and deliver technical presentations...
resume-library.com -
Biogen-South San Francisco
Support regulatory aspects of clinical trials from start-up to completion.
• Author regulatory documents and represent the company in external regulatory matters.
• Direct timelines for regulatory filings to meet project deadlines.
• Develop and review...
smartrecruiters.com -
AbbVie-South San Francisco
reports
Author and deliver technical presentations...
resume-library.com -
Pfizer-South San Francisco
clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program.
+ Responsible for scientific oversight, data integrity and quality of the clinical trial(s).
+ Authors...
dejobs.org -
ORIC Pharmaceuticals-South San Francisco
and DP based upon batch history data and control strategy.
Manage and provide technical guidance during investigations/ quality events at CDMOs/ CROs in collaboration with quality.
Author and review technical reports, technical data packages...
resume-library.com -
ORIC Pharmaceuticals-South San Francisco
and DP based upon batch history data and control strategy.
Manage and provide technical guidance during investigations/ quality events at CDMOs/ CROs in collaboration with quality.
Author and review technical reports, technical data packages...
resume-library.com -
AbbVie-South San Francisco
Represent the cell culture development group in cross-functional meetings and collaborate closely with cell line, purification, analytical and formulation development leads to meet project timelines
Author and review technical reports, GMP campaign summary...
resume-library.com -
Aequor Technologies LLC-South San Francisco
and supervisor.
Provide routine updates to the Supervisor on progress, status, and issues associated with assigned tasks.
Author or revise Internal Procedures or Standard Operating Procedures (as applicable).
Communicate with customers in a professional manner...
resume-library.com -
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