Author Jobs in Boston
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Apsida Life ScienceBoston
Contribute to clinical development plans and overall program strategy
• Interpret safety/efficacy data and support decision-making
• Author and review key clinical and regulatory documents
• Collaborate cross-functionally (clinical ops, translational...
Quadratic 3D, Inc.Boston
skills.
• Demonstrated ability to independently drive an idea from conception to project completion.
• Evidence of strong collaboration and teamwork talents/skills.
• Strong publication record, both as lead author and as contributor to other...
Net2Source (N2S)Boston
excellent writing and communication skills, and the ability to guide non-quality personnel through complex quality processes efficiently and without unnecessary burden.
Responsibilities:
Key Responsibilities
Partner with SMEs to author, document...
Bostonpharmiweb.jobs
clinical development in cross-functional teams such as Safety Management, Benefit-Risk Assessment, and Evidence Strategy Teams.
• Author or contribute to key documents, including Clinical Development Plans, Investigator Brochures, Study Protocols...
Apsida Life ScienceBoston
and protocol development
• Contribute to clinical development plans and overall program strategy
• Interpret safety/efficacy data and support decision-making
• Author and review key clinical and regulatory documents
• Collaborate cross-functionally (clinical...
Takeda PharmaceuticalBoston
on product specific value evidence topics, as applicable.
• Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.
• Monitor and anticipate trends that impact both the regulatory and access environments...
Quadratic 3D, Inc.Boston
ability to independently drive an idea from conception to project completion.
• Evidence of strong collaboration and teamwork talents/skills.
• Strong publication record, both as lead author and as contributor to other projects.
Preferred Qualifications...
Takeda PharmaceuticalBoston
value evidence topics, as applicable.
• Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.
• Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product...
Takeda PharmaceuticalBoston
as applicable.
• Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.
• Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan(s) and adopt...
Takeda PharmaceuticalBoston
value evidence topics, as applicable.
• Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.
• Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product...
McCarter & English, LLPBoston
topical issues and evaluating lawyers to provide commentary or author articles.
• Creating key messaging to strategically position the practice groups.
• Conducting research on industry trends, prospective clients, and competitors’ marketing activities...
Takeda PharmaceuticalBoston
on product specific value evidence topics, as applicable.
• Develop/author and execute global regulatory strategies for complex strategies. May oversee execution.
• Monitor and anticipate trends that impact both the regulatory and access environments...
Blonde Inc.Bostonappcast.io
at Hemab Therapeutics. This role requires both strategic thinking to assemble evidence generation plans and hands-on expertise to author manuscripts, develop scientific platforms, and manage publication timelines.
We do it because we believe when...
Takeda PharmaceuticalBoston
respective functions.
Labeling Documents Authoring, Submission, and Labeling Negotiations
• Authors new/revised TLP, CCDS, USPI and/or EU SmPC for assigned products, obtaining input and approval from all relevant functional areas with appropriate...
Abacus Technology CorporationBoston
and implementing corrective actions. * Ensure the rigorous application of cybersecurity and cryptographic policies, principles, and practices throughout the system development lifecycle. * Author, monitor, and record system information in applicable databases...
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