Participate in vendor review, selection, and negotiations * Assist in planning and execution of ... editing therapeutics and familiarity with LNP or AAV-based drug development * Ability to work ...
Participate in vendor review, selection, and negotiations * Assist in planning and execution of ... editing therapeutics and familiarity with LNP or AAV-based drug development * Ability to work ...
Administrative Assistant I
Boston, MA · On-site
$19.50 - $26.25/hr
Strong knowledge of PowerPoint presentation development and editing for client meetings. * An Administrative Assistant will make use of several application systems including: * ivalua - Supplies and ...
Quick apply
Administrative Assistant I
Boston, MA · On-site
$19.50 - $26.25/hr
Strong knowledge of PowerPoint presentation development and editing for client meetings. * An Administrative Assistant will make use of several application systems including: * ivalua - Supplies and ...
Policy Compliance Assistant
Dedham, MA · On-site
$62K - $77K/yr
Shall assist in the development of follow-up action plans for all audits or inspections, based on ... editing, within PowerDMS. * Shall coordinate with department heads, as necessary, to complete the ...
New
Policy Compliance Assistant
Dedham, MA · On-site
$62K - $77K/yr
Shall assist in the development of follow-up action plans for all audits or inspections, based on ... editing, within PowerDMS. * Shall coordinate with department heads, as necessary, to complete the ...
New
Policy Compliance Assistant
Dedham, MA · On-site
Shall assist in the development of follow-up action plans for all audits or inspections, based on ... editing, within PowerDMS. * Shall coordinate with department heads, as necessary, to complete the ...
New
Quick apply
Policy Compliance Assistant
Dedham, MA · On-site
Shall assist in the development of follow-up action plans for all audits or inspections, based on ... editing, within PowerDMS. * Shall coordinate with department heads, as necessary, to complete the ...
New
Assistant Director of Admission Strategy and Communications
Wellesley, MA · On-site
$65K - $70K/yr
... development and execution of this content. * Produce compelling, strategically-driven digital ... Expertise in video and image editing; Some experience in graphic design preferred. * Understanding ...
Assistant Director of Admission Strategy and Communications
Wellesley, MA · On-site
$65K - $70K/yr
... development and execution of this content. * Produce compelling, strategically-driven digital ... Expertise in video and image editing; Some experience in graphic design preferred. * Understanding ...
... development and execution of this content. * Produce compelling, strategically-driven digital ... Expertise in video and image editing; Some experience in graphic design preferred. * Understanding ...
... development and execution of this content. * Produce compelling, strategically-driven digital ... Expertise in video and image editing; Some experience in graphic design preferred. * Understanding ...
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... Their role will also drive our drug product development of our targeting moieties for our LNP ...
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... Their role will also drive our drug product development of our targeting moieties for our LNP ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
Our toolkit of RNA-targeting modalities including RNAi silencing and RNA editing provides us with ... Review clinical data from all phases of development and assist in generating study reports and ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
Our toolkit of RNA-targeting modalities including RNAi silencing and RNA editing provides us with ... Review clinical data from all phases of development and assist in generating study reports and ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
Our toolkit of RNA-targeting modalities including RNAi silencing and RNA editing provides us with ... Review clinical data from all phases of development and assist in generating study reports and ...
Director, Clinical Development
Lexington, MA · On-site
$89K - $122K/yr
Our toolkit of RNA-targeting modalities including RNAi silencing and RNA editing provides us with ... Review clinical data from all phases of development and assist in generating study reports and ...
Senior Director, State Government Affairs
Cambridge, MA · On-site
$260K - $320K/yr
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... The individual will also assist, as necessary, in Beam's federal government affairs strategy ...
Senior Director, State Government Affairs
Cambridge, MA · On-site
$260K - $320K/yr
Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology ... The individual will also assist, as necessary, in Beam's federal government affairs strategy ...
Senior Clinical Trial Associate
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
New
Senior Clinical Trial Associate
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
New
Senior Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
Senior Clinical Trial Associate
Waltham, MA · On-site
$115K - $159K/yr
Support Trial Master File (TMF) management, including document filing and quality control * Assist with development, editing, and distribution of key study documents (e.g., informed consent forms ...
Process Development Research Scientist
Charlestown, MA · On-site
$60K - $96K/yr
They assist their PI in the training and supervision of other laboratory personnel and in a wide ... Familiarity with CRISPR/Cas-based genome editing technologies. Experience with viral vector ...
Process Development Research Scientist
Charlestown, MA · On-site
$60K - $96K/yr
They assist their PI in the training and supervision of other laboratory personnel and in a wide ... Familiarity with CRISPR/Cas-based genome editing technologies. Experience with viral vector ...
Content Integration & Messaging Assistant
Boston, MA · On-site
$48K - $70K/yr
This role will work closely with the marketing and client development department at large and other ... Support auditing, drafting, editing and quality control of content across formats to ensure ...
Content Integration & Messaging Assistant
Boston, MA · On-site
$48K - $70K/yr
This role will work closely with the marketing and client development department at large and other ... Support auditing, drafting, editing and quality control of content across formats to ensure ...
Content Integration & Messaging Assistant
Boston, MA · On-site
$48K - $70K/yr
This role will work closely with the marketing and client development department at large and other ... Support auditing, drafting, editing and quality control of content across formats to ensure ...
Content Integration & Messaging Assistant
Boston, MA · On-site
$48K - $70K/yr
This role will work closely with the marketing and client development department at large and other ... Support auditing, drafting, editing and quality control of content across formats to ensure ...
Senior QA Specialist
Cambridge, MA · On-site
$110K - $120K/yr
... Editor! Decoding The Role ... The primary focus of this role in the next 12 months is to advance our lead in vivo development ...
Quick apply
Senior QA Specialist
Cambridge, MA · On-site
$110K - $120K/yr
... Editor! Decoding The Role ... The primary focus of this role in the next 12 months is to advance our lead in vivo development ...
Senior QA Specialist
Cambridge, MA · On-site
$110K - $120K/yr
... Editor! Decoding The Role ... The primary focus of this role in the next 12 months is to advance our lead in vivo development ...
Senior QA Specialist
Cambridge, MA · On-site
$110K - $120K/yr
... Editor! Decoding The Role ... The primary focus of this role in the next 12 months is to advance our lead in vivo development ...
Marketing Coordinator
Boston, MA · On-site
$46K - $63K/yr
Proposal & Content Development: Assist in the creation of compelling custom proposals, SF330 forms and other uniquely branded marketing collateral in response to RFPs and RFQs. * Writing & Editing:
Quick apply
Marketing Coordinator
Boston, MA · On-site
$46K - $63K/yr
Proposal & Content Development: Assist in the creation of compelling custom proposals, SF330 forms and other uniquely branded marketing collateral in response to RFPs and RFQs. * Writing & Editing:
Marketing Coordinator
Boston, MA · On-site
$46K - $63K/yr
Proposal & Content Development: Assist in the creation of compelling custom proposals, SF330 forms and other uniquely branded marketing collateral in response to RFPs and RFQs. * Writing & Editing:
Marketing Coordinator
Boston, MA · On-site
$46K - $63K/yr
Proposal & Content Development: Assist in the creation of compelling custom proposals, SF330 forms and other uniquely branded marketing collateral in response to RFPs and RFQs. * Writing & Editing:
... agenda development, and preparation of meeting materials. * Serve as recorder for standing ... Coordinate the editing and publication of the CAS Faculty Manual, ensuring alignment with actions ...
... agenda development, and preparation of meeting materials. * Serve as recorder for standing ... Coordinate the editing and publication of the CAS Faculty Manual, ensuring alignment with actions ...
Assistant Development Editor information
See Boston, MA salary details
$25.5K - $29.6K
2% of jobs
$29.6K - $33.7K
2% of jobs
$33.7K - $37.8K
2% of jobs
$37.8K - $41.9K
13% of jobs
$43.7K is the 25th percentile. Wages below this are outliers.
$41.9K - $46K
15% of jobs
$46K - $50.1K
16% of jobs
The median wage is $50.6K / yr.
$50.1K - $54.2K
9% of jobs
$54.2K - $58.3K
9% of jobs
$61.5K is the 75th percentile. Wages above this are outliers.
$58.3K - $62.4K
9% of jobs
$62.4K - $66.5K
9% of jobs
$66.5K - $70.6K
14% of jobs
$25.5K
$55.6K
$70.6K
How much do assistant development editor jobs pay per year?
What is an assistant development editor?
How does an assistant development editor typically collaborate with authors and other editorial staff during the manuscript development process?
What are the key skills and qualifications needed to thrive as an assistant development editor, and why are they important?
What is the difference between Assistant Development Editor vs Development Editor?
| Aspect | Assistant Development Editor | Development Editor |
|---|---|---|
| Credentials | Bachelor's degree in English, Publishing, or related field; some experience in editing | Bachelor's or master's degree; extensive editing experience |
| Work Environment | Assists in editing, proofreading, and project coordination within publishing teams | Leads editing projects, makes content decisions, and manages editorial workflows |
| Responsibilities | Supports development tasks, reviews content, and assists senior editors | Oversees content development, edits manuscripts, and ensures quality standards |
The Assistant Development Editor typically supports the development process under supervision, focusing on editing and coordination. The Development Editor takes on more responsibility, leading content development and making editorial decisions. Both roles require strong editing skills and familiarity with publishing workflows, but the Development Editor has a higher level of responsibility and experience.
What are the most commonly searched types of Development Editor jobs in Boston, MA?
The most popular types of Development Editor jobs in Boston, MA are:
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For Assistant Development Editor jobs in Boston, MA, the most frequently searched job titles are:
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The top searched job categories for Assistant Development Editor jobs in Boston, MA are:

Senior Clinical Trial Manager
Cambridge, MA • On-site
Full-time
Re-posted 10 days ago
Job description
Arbor Biotechnologies, a clinical stage, next-generation gene editing company based in Cambridge, MA, is advancing a portfolio of first-in-class genomic medicines addressing serious diseases for which there are no existing functional cures, with a CNS pipeline initially prioritizing multiple ALS targets and a co-developed, clinical program, ABO-101, for the treatment of primary hyperoxaluria type 1. The company's unique breadth of gene editing technologies goes beyond the limitations of early editing approaches to unlock access to new gene targets and expand the therapeutic reach of genomic medicines. For more information, please visit: arbor.bio.
Who are you?
Passionate, determined, and accountable. Curious, resourceful, innovative, forward thinking, and resilient. Authentic, humble, open-minded and puts team above self. At Arbor, our people embrace these qualities, so if this sounds like you then please read on!
About the Role:
The Senior Clinical Trial Manager will be at the forefront of our early phase studies. The role will report into the Senior Director of Clinical Operations and will be in a highly visible role for a novel class of gene editing therapeutics in rare genetic diseases. The role will be a key contributor to implementing and executing clinical trials from start-up to close-out. The role will be accountable for clinical trial management, trial master file, site monitoring, study start-up activities, and CRO management.
What You Can Expect:
- Overall responsibility for the management of clinical study sites and external vendors while adhering to budget, scope and schedule requirements in accordance with GCP and ICH guidelines
- Develop and effectively manage budgets and timelines for assigned clinical studies
- Participate in the development clinical operations study plans, study templates and SOP/WI
- Participate in creation and review of study protocols, Informed Consent Forms (ICFs), Case Report Forms (CRFs), Statistical Analysis Plans (SAPs), Clinical Study Reports (CSRs), and other clinical documents to ensure seamless integration between clinical objectives and study performance
- Assist in management of cross functional study teams and establishing/maintaining key internal and external stakeholder relationships to ensure study milestones are met
- Track and oversee lab sample transfers from patients to sites to clinical lab vendors
- Proactively identify and resolve issues and manage escalation as appropriate
- Manage timelines for Safety Review Boards, Data Monitoring Committee and Data Cuts
- Oversee maintenance of trial documentation and master file, data validation, and completion guidelines
- Participate in vendor review, selection, and negotiations
- Assist in planning and execution of Investigator Meetings as required. Establish working relationships with clinical and internal and external medical experts to optimize and implement clinical studies
- Represent the company externally and travel to investigative sites as needed
What You Bring:
- Bachelor's degree and 6+ years or relevant and progressive clinical operations experience working in the pharmaceutical and/or biotech industry, preferably a mix of both
- Experience managing early-phase clinical studies in rare diseases
- Solid well-grounded experience in setup, execution and operational management of US and global clinical trials (delivered on time, within budget, and with high quality)
- Experience in ethics and regulatory dossier submissions (e.g., pre-IND, IND, Scientific Advice, CTA)
- Strong knowledge of GCP/ICH, drug development process, and other relevant guidelines for clinical research activities
- Proven track record of experience working with CROs, functional service providers and third-party vendors; strong contract negotiation abilities and thorough understanding of all financial aspects of contracts
- Proficient project management skills (e.g., Smartsheet, MS office or equivalent)
- Scientifically adept and great communication and interpersonal skills
- Knowledge of mRNA, RNAi, gene therapy or gene editing therapeutics and familiarity with LNP or AAV-based drug development
- Ability to work independently and collaboratively in a fast-paced, matrixed, team environment consisting of internal and external team members
- Excellent planning, organization, and time management skills
- Motivated individuals who want to roll up their sleeves and apply drug development knowledge and experience to develop gene-editing therapies in a startup environment
- Flexibility to travel domestically and internationally as required
Our Values:
Our values govern the work we do at Arbor, and we're hoping that they resonate as strongly with you as they do with us!
- Purposeful Action: Driven by outcomes, guided by purpose
- Bold Resilience: Speak boldly, embrace change, grow forward
- Humble Authenticity: Be real, value the uniqueness of others, elevate all
The anticipated salary range for candidates for this role will be $145,000 - $170,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, industry knowledge, technical skills, and other factors that may prove relevant during the interview process.
We promote diversity and inclusion not just in our recruitment processes, but in everything we do. We're an equal opportunity employer and we will continue to ensure our recruitment process is free of bias and our workplace is inclusive, positive, and free of discrimination and respecting of all backgrounds and beliefs.
About Arbor Biotechnologies
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
11 - 50 Employees
Headquarters location
Cambridge, MA, US
Year founded
2016