We are seeking a Scientific Writer with strong nonclinical regulatory experience to support the ... Manage multiple regulatory writing efforts in parallel, balancing priorities across programs and ...
We are seeking a Scientific Writer with strong nonclinical regulatory experience to support the ... Manage multiple regulatory writing efforts in parallel, balancing priorities across programs and ...
Our novel scientific approach targets upstream C1q to block the classical complement inflammatory ... The Senior Director, Medical and Scientific Writing plays a critical role within the organization.
Our novel scientific approach targets upstream C1q to block the classical complement inflammatory ... The Senior Director, Medical and Scientific Writing plays a critical role within the organization.
Grant Writer / Staff Scientist, Sanjana Lab
New York, NY ยท On-site
$62K - $78K/yr
Manages the scientific writing process, including proposal management, team-building and coordination; establishing timelines and deliverables; * Provides draft preparation, review and revision of ...
Grant Writer / Staff Scientist, Sanjana Lab
New York, NY ยท On-site
$62K - $78K/yr
Manages the scientific writing process, including proposal management, team-building and coordination; establishing timelines and deliverables; * Provides draft preparation, review and revision of ...
Our novel scientific approach targets upstream C1q to block the classical complement inflammatory ... The Senior Director, Medical and Scientific Writing plays a critical role within the organization.
Our novel scientific approach targets upstream C1q to block the classical complement inflammatory ... The Senior Director, Medical and Scientific Writing plays a critical role within the organization.
Scientific Director (Oncology)
Cranbury, NJ ยท On-site
$130K - $140K/yr
Mentor and develop Medical Writers and Editors, providing clear direction and guidance on scientific writing best practices, workload prioritization, and quality standards. * Attend live events ...
Scientific Director (Oncology)
Cranbury, NJ ยท On-site
$130K - $140K/yr
Mentor and develop Medical Writers and Editors, providing clear direction and guidance on scientific writing best practices, workload prioritization, and quality standards. * Attend live events ...
Staff Scientist / Grant Writer, Sanjana Lab
Manhattan, NY ยท On-site
$62K - $78K/yr
Manages the scientific writing process, including proposal management, team-building and coordination; establishing timelines and deliverables; * Provides draft preparation, review and revision of ...
Staff Scientist / Grant Writer, Sanjana Lab
Manhattan, NY ยท On-site
$62K - $78K/yr
Manages the scientific writing process, including proposal management, team-building and coordination; establishing timelines and deliverables; * Provides draft preparation, review and revision of ...
Program Manager, Scientific Outreach and Communications
Worcester, MA ยท On-site
$80K - $90K/yr
Collaborate with scientific writers, faculty, and trainees to support preparation of fellowship applications, including: * Edit application components (e.g., research statements, training plans ...
Program Manager, Scientific Outreach and Communications
Worcester, MA ยท On-site
$80K - $90K/yr
Collaborate with scientific writers, faculty, and trainees to support preparation of fellowship applications, including: * Edit application components (e.g., research statements, training plans ...
Director, Medical Writing
Cambridge, MA ยท On-site
Director, Medical Writing At Merida Biosciences, we are pioneering true precision medicines for ... Maintain high standards of scientific accuracy, quality, consistency, and clarity. * Drive ...
New
Quick apply
Director, Medical Writing
Cambridge, MA ยท On-site
Director, Medical Writing At Merida Biosciences, we are pioneering true precision medicines for ... Maintain high standards of scientific accuracy, quality, consistency, and clarity. * Drive ...
New
We are seeking a Scientific Writer with strong nonclinical regulatory experience to support the ... Manage multiple regulatory writing efforts in parallel, balancing priorities across programs and ...
We are seeking a Scientific Writer with strong nonclinical regulatory experience to support the ... Manage multiple regulatory writing efforts in parallel, balancing priorities across programs and ...
Medical Writer III
Maple Grove, MN ยท On-site
Bachelor's degree in biomedical sciences, medicine, or related field] * 6-8 years of experience in medical or scientific writing (preferably in medical devices or pharma) * Hands-on experience ...
Quick apply
Medical Writer III
Maple Grove, MN ยท On-site
Bachelor's degree in biomedical sciences, medicine, or related field] * 6-8 years of experience in medical or scientific writing (preferably in medical devices or pharma) * Hands-on experience ...
... and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior ...
... and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior ...
... and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior ...
... and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. The Senior ...
Associate Director, Medical Writing
San Diego, CA ยท On-site +1
We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients . Position Summary: The Associate Director, Medical Writing is ...
Associate Director, Medical Writing
San Diego, CA ยท On-site +1
We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients . Position Summary: The Associate Director, Medical Writing is ...
Scientific Director (Oncology)
Charleston, WV ยท Remote
$130K - $140K/yr
Mentor and develop Medical Writers and Editors, providing clear direction and guidance on scientific writing best practices, workload prioritization, and quality standards. * Attend live events ...
Scientific Director (Oncology)
Charleston, WV ยท Remote
$130K - $140K/yr
Mentor and develop Medical Writers and Editors, providing clear direction and guidance on scientific writing best practices, workload prioritization, and quality standards. * Attend live events ...
Performs scientific writing (e.g. abstracts, manuscripts, presentations). Organizes and incorporates information for documents, such as references, graphics, tables, and data listings. Ensures ...
Performs scientific writing (e.g. abstracts, manuscripts, presentations). Organizes and incorporates information for documents, such as references, graphics, tables, and data listings. Ensures ...
Scientific Research Analyst
Philadelphia, PA ยท On-site
Ensure all written content meets the highest standards of scientific accuracy and integrity. * Perform other relevant duties as assigned. Qualifications * PhD or equivalent doctoral degree in ...
Scientific Research Analyst
Philadelphia, PA ยท On-site
Ensure all written content meets the highest standards of scientific accuracy and integrity. * Perform other relevant duties as assigned. Qualifications * PhD or equivalent doctoral degree in ...
Performs scientific writing (e.g. abstracts, manuscripts, presentations). * Organizes and incorporates information for documents, such as references, graphics, tables, and data listings. * Ensures ...
Performs scientific writing (e.g. abstracts, manuscripts, presentations). * Organizes and incorporates information for documents, such as references, graphics, tables, and data listings. * Ensures ...
Minimum of 10 years of scientific writing/communications/clinical or related experience in Pharma/Biotech industry or Medical Communications (3 years for doctorate candidate) * Scientific ...
Minimum of 10 years of scientific writing/communications/clinical or related experience in Pharma/Biotech industry or Medical Communications (3 years for doctorate candidate) * Scientific ...
OR ยท On-site
Design, write, and present scientific posters and podium presentations for key conferences (ASM Microbe, ESCMID Global, IDSA IDWeek, ADLM, and others) * Lead the writing and submission of peer ...
OR ยท On-site
Design, write, and present scientific posters and podium presentations for key conferences (ASM Microbe, ESCMID Global, IDSA IDWeek, ADLM, and others) * Lead the writing and submission of peer ...
Scientific Research Analyst
Philadelphia, PA ยท On-site +1
Ensure all written content meets the highest standards of scientific accuracy and integrity. * Perform other relevant duties as assigned. * PhD or equivalent doctoral degree in biological sciences or ...
Scientific Research Analyst
Philadelphia, PA ยท On-site +1
Ensure all written content meets the highest standards of scientific accuracy and integrity. * Perform other relevant duties as assigned. * PhD or equivalent doctoral degree in biological sciences or ...
Scientific Writing information
See salary details
$11K - $17.2K
0% of jobs
$17.2K - $23.5K
0% of jobs
$23.5K - $29.7K
0% of jobs
$29.7K - $35.9K
0% of jobs
$35.9K - $42.1K
0% of jobs
$42.1K - $48.4K
0% of jobs
$48.4K - $54.6K
0% of jobs
$54.6K - $60.8K
0% of jobs
$60.8K - $67K
12% of jobs
$68.3K is the 25th percentile. Wages below this are outliers.
$67K - $73.3K
62% of jobs
$73.4K is the 75th percentile. Wages above this are outliers.
$73.3K - $79.5K
26% of jobs
$11K
$70.5K
$79.5K
How much do scientific writing jobs pay per year?
What are the key skills and qualifications needed to thrive as a Scientific Writer, and why are they important?
How can I become a scientific writer?
How does a scientific writer typically collaborate with researchers and subject matter experts during the publication process?
How much do scientific writers get paid?
What is a scientific writer?
What is scientific writing?
Is scientific writing a good career?
What is the difference between Scientific Writing vs Scientific Editing?
| Aspect | Scientific Writing | Scientific Editing |
|---|---|---|
| Primary Focus | Creating original scientific content, such as research papers and reports | Reviewing and improving existing scientific documents for clarity and accuracy |
| Skills Required | Strong writing, research, and communication skills | Attention to detail, editing, and knowledge of scientific terminology |
| Work Environment | Research institutions, academic journals, biotech companies | Publishing houses, academic journals, research organizations |
| Common Certifications | Science degrees, writing certifications | Editing certifications, scientific editing training |
Scientific Writing involves creating original scientific documents, while Scientific Editing focuses on refining and improving existing content. Both roles require a solid understanding of science and strong communication skills, but they serve different stages of the publication process.

Other
Posted 20 days ago
Job description
The Opportunity:
We are seeking a Scientific Writer with strong nonclinical regulatory experience to support the authoring and integration of nonclinical content for U.S. and global regulatory submissions. This role focuses on developing and integrating nonclinical content beyond INDs and NDAs, including briefing documents, Investigator Brochures, responses to health authority questions, and other submission-related materials across the U.S., Europe, and Asia.
As a strategic scientific integrator, this individual will translate complex RAS biology and translational pharmacology into clear, compelling regulatory narratives that reflect RevMed's deep mechanistic understanding of RAS signaling and frontier targets. The role partners closely with nonclinical subject matter experts (SMEs) in pharmacology, toxicology, and DMPK, as well as Regulatory Affairs, Regulatory Operations, and Medical Writers, to ensure nonclinical strategy and content are scientifically rigorous, aligned, and submission-ready.
The Scientific Writer will leverage structured source documents, document management systems, and emerging AI-enabled tools to improve efficiency, consistency, and scalability of nonclinical regulatory writing. This role requires strong organizational skills and the ability to manage multiple programs and cross-functional inputs simultaneously in a fast-paced, scientifically rigorous environment.
Key Responsibilities
Author, integrate, and edit nonclinical sections of regulatory documents across multiple submission types, including INDs, NDAs, briefing documents, amendments, and response to health authority requests.
Safeguard and articulate the scientific rationale underlying RevMed's RAS(ON) and companion inhibitor programs across regulatory communications.
Develop clear, hypothesis-driven regulatory narratives that integrate pharmacology, toxicology, and DMPK data, and engage as a critical scientific thought partner to these functions to strengthen mechanistic coherence, regulatory positioning, and alignment with global regulatory expectations (FDA, EMA, and select Asian agencies).
Collaborate closely with project Medical Writers to ensure nonclinical sections are delivered in alignment with overall timelines and coordinated with related document sections.
Ensure scientific consistency across programs to preserve and extend RevMed's reputation for rigor and mechanistic depth.
Manage multiple regulatory writing efforts in parallel, balancing priorities across programs and functions in a fast-paced environment.
Utilize Regulatory information management systems (e.g., Veeva) and AI-enabled writing tools to support authoring, review, and lifecycle management of regulatory documents.
Contribute to templates, guidance, and best practices for global nonclinical regulatory documentation.
Drive continuous improvement of nonclinical authoring standards, templates, and knowledge management systems.
Capture and institutionalize lessons learned from prior submissions to improve quality, consistency, and efficiency across programs and regions.
Required Skills, Experience and Education:
Advanced degree (PhD preferred; MS considered) in a relevant nonclinical scientific discipline.
Demonstrated experience authoring or substantially contributing to nonclinical sections of regulatory submissions across multiple document types.
Strong working knowledge of pharmacology, toxicology, and DMPK and their integration into regulatory narratives.
Demonstrated ability to synthesize complex mechanistic datasets into coherent, hypothesis-driven regulatory narratives.
Comfortable engaging deeply in data discussions with subject matter experts and operating in a culture of scientific debate and rigorous review.
Familiarity with range of regulatory expectations including those beyond the U.S. such as European and/or Asian health authorities.
Proven ability to manage multiple projects concurrently and work effectively across functions.
Excellent written communication skills, attention to detail, and a collaborative, solutions-oriented mindset.
Preferred Skills:
Industry experience as a Scientific or Medical Writer.
Experience supporting global regulatory submissions (FDA, EMA, etc.).
Proficiency with Veeva or similar Regulatory information management systems platforms.
Experience leveraging AI-enabled tools for scientific or regulatory writing.
Comfortable operating in a dynamic, evolving research and development environment. #LI-Hybrid ย #LI-LN1