Author Jobs in Princeton (NJ)
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Search Results - Author Jobs in Princeton (NJ)
MMS-Princeton (NJ)
experience
• The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
• Substantial clinical study protocol experience, as lead author, required
• Experience leading and managing teams while authoring...
mindmatch.ai -
Diverse Lynx-Princeton (NJ)
and technical questions from customers.
3. Author response to RFX, Defend solution with internal and end customer.
4. Build & manage opportunity pipeline with proactive engagement with internal and external customers.
5. Demonstrate TCS offerings...
resume-library.com -
Genmab-Princeton (NJ)
monitoring, liaise with investigators and site personnel, perform preliminary and exploratory data analyses on clinical trials, author clinical study reports, provide input on publication materials, and participate in advisory boards.
• Establish productive...
Katalyst Healthcares & Life Sciences-Princeton (NJ)
Annual Product Quality Reports (APQR)
Review statistical analysis that measures process capability and trending performance.
Ability to author quality agreements with contract development, manufacturing, and laboratory organizations.
Awareness...
resume-library.com -
Princeton (NJ)
in at least one research project, and being a co-author in other projects, providing opportunities for developing their own ideas and contributing to innovation inputs to the lab.
Responsibilities:
• Expand/develop code in R for conducting multivariate...
icims.com -
Dr Reddy's Laboratories Limited-Princeton (NJ)
for product stability and FDA, and other agency submissions.
Author, review, and coordinate approvals for documentation to support all activities as needed.
Provide packaging structural engineering, development and design support.
Coordinate structural...
resume-library.com -
Genmab-Princeton (NJ)
Document all template related issues, and identify resolutions
Responsible for creating and providing training to authors utilizing the submission templates.
Participate as an active team member and provide expertise to project teams as required...
ACADIA Pharmaceuticals Inc.-Princeton (NJ)
publication 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...
appcast.io -
Princeton (NJ)
and production of communications materials.
• Author, review, and edit press releases. Create presentation materials as requested.
Outreach and Collaboration: Work collaboratively with HMEI colleagues and others including personnel in the offices of University...
icims.com -
Taiho Oncology, Inc.-Princeton (NJ)
Participates in the preparation of protocols and Case Report Forms (eCRFs), data management, monitoring, communication, and other project plans.
• Authors and leads the coordination of study specific documents such as Informed Consent.
• Works with CROs...
appcast.io -
Princeton (NJ)
data towards development
• Serving as principal functional author for Regulatory submissions, study reports, and publications
• Independently synthesizes and/or contributes to plans (e.g., trial design, development strategy, regulatory strategy) based...
pharmiweb.jobs -
Princeton (NJ)
by the target audience
• Collaborates with others to develop key messages for complex clinical/regulatory documents
• Authors, reviews, and/or edits documents to support clinical trials and regulatory submissions, which may include:
stylelist:style:type:circle...
tiptopjob.com -
Princeton (NJ)
for Network services.
• Prepare and author consultant and contractor RFI and RFP material
• Identify project risks and develop risk mitigation strategies
• Oversee and prepare accurate project documentation for all phases of the project
• Track and submit...
icims.com -
Princeton (NJ)
authors and/or reviews protocol, statistical analysis plan, clinical study reports, associated publications, and other study level documents
• Presents summary data and analyses results, in a clear, concise, complete, and transparent manner
• Provides...
pharmiweb.jobs -
Princeton (NJ)
members.
Key Responsibilities
• Collaborates in design of clinical study including methodology, data analysis & interpretation, and reporting of study results.
• Authors and/or reviews protocol synopsis, protocol, statistical analysis plans, case-report...
pharmiweb.jobs -
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