Author Jobs in Massachusetts
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Search Results - Author Jobs in Massachusetts
Wondermore, Inc.-Boston-
Director of Development (20 hours/week)
Wondermore’s mission is to spark a love of books and reading and strengthen literacy skills by connecting Boston-area students with authors and illustrators who reflect our vibrant and diverse communities...
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Clinical Dynamix, Inc.-Burlington (MA)-jobvertise.com-
and
rigorous data analysis.
Provide high-quality statistical support across clinical programs, ensuring scientific
robustness and alignment with development goals.
Design and refine clinical trial methodologies; author study synopses and protocols...
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Wondermore, Inc.-Boston-
Job Description
Director of Development (20 hours/week)
Wondermore’s mission is to spark a love of books and reading and strengthen literacy skills by connecting Boston-area students with authors and illustrators who reflect our vibrant...
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The Lotus Group LLC-Cambridge-
We are seeking an experienced Director of Biostatistics to lead statistical strategy and execution for complex, late-stage clinical development programs. In this role, you will design innovative clinical trials, author statistical sections...
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AMN Healthcare Allied-Newton Lower Falls-
/n/n
Facility Location
Newton Lower Falls is a village of Newton, Massachusetts and is situated on the Charles River. The village is also home of the famous landmark known as the Lower Falls Wine Company and the well-known author Sarah Fuller, who...
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Intellectt Inc-Marlborough (MA)-
Process Validation and TMV activities
• Develop and maintain PFMEAs, CAPAs, CPQs, and CTQs
• Author and update protocols, reports, and quality documentation
• Partner with Manufacturing Engineering, Validation, and Operations teams
Required Qualifications...
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AMN Healthcare Allied-Newton Lower Falls-
as the Lower Falls Wine Company and the well-known author Sarah Fuller, who taught Helen Keller. This area is now a suburban neighborhood and located close to the park at the old Hamilton elementary school and bordered on the northwest by the Leo J.
Martin...
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Terrestrial-Woburn (MA)-
validate, and characterize GMP-compliant purity, SEC, and content methods for intermediates and drug products, with a strong emphasis on chromatographic workflows.
• Author and execute cGMP method qualification and validation protocols, prepare reports...
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Sironax-Waltham (MA)-
Maintain alignment across global teams, including effective collaboration with US- and China-based stakeholders across multiple time zones.
• Ensure compliance with CDISC standards, ICH guidelines, and FDA/EMA regulatory requirements.
• Author and review...
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Meet Life Sciences-Watertown (MA)-
facilities, automation systems, and infrastructure.
• Develop and execute validation documentation, including plans, risk assessments, IQ/OQ/PQ protocols, traceability matrices, and summary reports.
• Author, review, and approve SOPs, change controls...
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SOKOL GxP Services-Devens-workable.com-
URS, DQ, validation plans, IOQ protocols, software test scripts, configuration specifications, risk assessments, and qualification summary reports.
• Author and execute computer system validation scripts using ALM or paper-based methods.
• Own change...
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Takeda Pharmaceutical-Boston-
significant synthesis investment
• Oversee repeat-dose, genetic toxicology, safety pharmacology studies as programs progress; ensure GLP studies are scoped correctly and delivered on time and to quality
• Author and review nonclinical sections of INDs, CTAs...
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Worcester-icims.com-
the following credentials:
• A recent Ph.D. and/or M.D. degree in Biology, or a related field, with no more than 1 year of postdoctoral experience
• A 1^st author publication in a peer-reviewed scholarly journal from their Ph.D. and/or M.D. research
• Previous...
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Amazon-North Reading-amazon.jobs-
product performance into structured analyses, and author recommendation-focused deliverables that inform program decisions and shape how new robotic systems progress through RST's development lifecycle. You will design, develop, and maintain dashboards...
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Randstad-Norwood (MA)-randstadusa.com-
the manufacturing and testing network.
• Author, review, and oversee validation-related documents, including validation master plans, protocols, reports, and associated technical documentation, to ensure alignment with program needs and regulatory requirements...
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