Author Jobs in Princeton (NJ)
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Search Results - Author Jobs in Princeton (NJ)
Experis-Princeton (NJ)
Provides on-the-floor and on-site technical support to manufacturing when necessary.
Author, review and approve, as needed, various documents (eg. Batch records, SOPs).
Author, and approve protocol and reports in accordance with internal and external...
Katalyst Healthcares & Life Sciences-Princeton (NJ)
input in the design and development of case report forms and clinical study databases.
Reviews or author aCRF, SDTM and ADaM datasets specifications for datasets programming.
Requirements:
MS in Statistics, Computer Science, or a related field...
resume-library.com -
Princeton University-Princeton (NJ)
helping conduct experiments, analyze results, and co-author research publications.
• Develop, maintain, and improve our shared infrastructure for training / fine-tuning and prompting large AI models.
• Maintain software libraries/environment/GitHub...
mindmatch.ai -
Mindlance-Princeton (NJ)
with prospects/clients.
• Provide appropriate documentation and support clients in authoring CMC sections.
• Demonstrate strong oral and written communication skills. Author protocols, reports, risk assessments, SOPs, and batch records.
• Supervise, train...
resume-library.com -
Aditi Consulting-Princeton (NJ)
Standards, European Medical Device Directives, and other International Regulations.
• Facilitates Document Change Orders for corporate quality system documents including document changes and training.
• Collaborates with document authors to release...
mindmatch.ai -
Aditi Consulting-Princeton (NJ)
with document authors to release and implement of Global Standard Operating Procedures (GSOPs).
Participate to Change Review Board meetings.
Operate in company’s corporate document control and training systems to transact changes to quality system documents...
resume-library.com -
ACADIA Pharmaceuticals Inc.-Princeton (NJ)
strategy development and collaboration with both internal and external authors.
• Contribute in discussions with Development colleagues and ensure that MA (including HEOR) perspectives are provided and incorporated in Development plans.
• Other duties...
appcast.io -
Integrated Resources, Inc-Princeton (NJ)
Facilitates Document Change Orders for corporate quality system documents including document changes and training.
" Collaborates with document authors to release and implement of Global Standard Operating Procedures (GSOPs).
" Participate to Change Review...
resume-library.com -
Princeton (NJ)
author research publications.
• Develop, maintain, and improve our shared infrastructure for training / fine-tuning and prompting large AI models.
• Maintain software libraries/environment/GitHub repositories and support model use.
• Provide support...
icims.com -
Princeton (NJ)
expectations for clinical data per defined processes
• Authors, reviews/revises DM related study plans including Data Quality Management Plan, Data Validation Plans, Data Review Plan, eCRF Completion Guidelines and other study documents to ensure quality...
pharmiweb.jobs -
Ascendis Pharma-Princeton (NJ)
publications. Demonstrate the flexibility/adaptability necessary to collaborate with and interpret input from different therapeutic teams and authors.
• Learn and apply knowledge of therapeutic areas and assigned products to scientific publication tactics...
workable.com -
Princeton (NJ)
interactions and advisory board meetings as Senior Clinical Trial Physician
• Authors/drafts clinical content for CSRs, regulatory reports, briefing books and submission documents to support closure, clinical narratives, reporting and filling of the study...
pharmiweb.jobs -
Mindlance-Princeton (NJ)
Document Change Orders for corporate quality system documents including document changes and training.
• Collaborates with document authors to release and implement of Global Standard Operating Procedures (GSOPs).
• Participate to Change Review Board...
resume-library.com -
Princeton (NJ)
conventions and quality expectations for clinical data per defined processes
• Authors, reviews/revises DM related study plans including Data Quality Management Plan, Data Validation Plans, Data Review Plan, eCRF Completion Guidelines and other study documents...
pharmiweb.jobs -
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