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Remote Science Curriculum Writer Jobs in Missouri

Jobgether

You will take ownership of complex regulatory documents while combining scientific expertise ... Fully remote work environment with flexibility within Europe. * Opportunity to contribute to ...

Varsity Tutors

AP Computer Science A Tutor

Saint Louis, MO · Remote

$18 - $40/hr

Familiar with AP Computer Science A curriculum across ten units and common challenges such as understanding polymorphism, implementing recursive solutions, and writing correct code in free-response ...

Varsity Tutors

AP Computer Science A Tutor

Kansas City, MO · Remote

$18 - $40/hr

Familiar with AP Computer Science A curriculum across ten units and common challenges such as understanding polymorphism, implementing recursive solutions, and writing correct code in free-response ...

Varsity Tutors

AP Computer Science A Tutor

Columbia, MO · Remote

$18 - $40/hr

Familiar with AP Computer Science A curriculum across ten units and common challenges such as understanding polymorphism, implementing recursive solutions, and writing correct code in free-response ...

Harris

Associate Technical Writer

Louisiana, MO · Remote

Bachelor's degree in English, Communications, Technical Writing, Computer Science, or a related ... Fully remote team with flexible working hours * Mentorship and growth opportunities within a ...

Varsity Tutors

Middle School Science Tutor

Kansas City, MO · Remote

$18 - $40/hr

... writing lab reports. Emphasizes hands-on investigation and critical thinking, connecting science to environmental awareness, health, and technology applications. * Curriculum Awareness & Adaptive ...

Varsity Tutors

Middle School Science Tutor

Columbia, MO · Remote

$18 - $40/hr

... writing lab reports. Emphasizes hands-on investigation and critical thinking, connecting science to environmental awareness, health, and technology applications. * Curriculum Awareness & Adaptive ...

micro1 AI

Medical Writing Manager

Saint Louis, MO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Kansas City, MO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Varsity Tutors

Middle School Science Tutor

Saint Louis, MO · Remote

$18 - $40/hr

... writing lab reports. Emphasizes hands-on investigation and critical thinking, connecting science to environmental awareness, health, and technology applications. * Curriculum Awareness & Adaptive ...

micro1 AI

Medical Writing Manager

Columbia, MO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Independence, MO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

micro1 AI

Medical Writing Manager

Springfield, MO · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

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Remote Science Curriculum Writer information

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$25

$32

How much do remote science curriculum writer jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for remote science curriculum writer in Missouri is $25.21, according to ZipRecruiter salary data. Most workers in this role earn between $20.96 and $31.11 per hour, depending on experience, location, and employer.

What is a remote science curriculum writer?

A Remote Science Curriculum Writer creates educational materials, lesson plans, and assessments for science subjects while working from a remote location. They align content with academic standards, ensure clarity and accuracy, and adapt materials for different grade levels or educational needs. This role often involves collaborating with educators, instructional designers, and subject matter experts to develop engaging and effective science curricula. Strong research, writing, and editing skills are essential, along with a solid understanding of scientific concepts.

What are the typical daily responsibilities of a remote science curriculum writer?

As a Remote Science Curriculum Writer, your daily tasks may include researching and developing lesson plans, creating assessments, and aligning materials to educational standards such as NGSS. You will likely collaborate virtually with subject matter experts, editors, and instructional designers to refine and review content. Regular communication via email, project management platforms, and video calls is common, and you may participate in feedback sessions to continuously improve curriculum materials. This role offers flexibility in work hours but requires strong time management to meet project deadlines and ensure high-quality deliverables.

What are the key skills and qualifications needed to thrive as a remote science curriculum writer?

A Remote Science Curriculum Writer should have a strong background in science education, experience in curriculum design, and relevant academic qualifications such as a degree in science or education. Familiarity with learning management systems (LMS), digital content creation tools, and educational standards like Next Generation Science Standards (NGSS) is often required. Excellent written communication, attention to detail, and the ability to collaborate remotely are valuable soft skills in this position. These attributes are essential for producing engaging, standards-aligned content that effectively supports diverse learners and instructional goals.

What are popular job titles related to Remote Science Curriculum Writer jobs in Missouri? For Remote Science Curriculum Writer jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Remote Science Curriculum Writer jobs in Missouri look for? The top searched job categories for Remote Science Curriculum Writer jobs in Missouri are:
What cities in Missouri are hiring for Remote Science Curriculum Writer jobs? Cities in Missouri with the most Remote Science Curriculum Writer job openings:
Remote Science Curriculum Writer jobs near you
Infographic showing various Remote Science Curriculum Writer job openings in Missouri as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 79% Full Time, 16% Part Time, and 3% Contract. Highlights an 77% Physical, 4% Hybrid, and 19% Remote job distribution, with an average salary of $52,441 per year, or $25.2 per hour.

Senior/Principal Medical Writer

Jobgether

On-site, Remote

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior/Principal Medical Writer based in Netherlands.

Join a specialized medical writing team supporting the development of high-quality regulatory documentation for the global pharmaceutical industry. In this role, you will contribute to clinical development programs across multiple therapeutic areas, partnering with scientific teams and industry stakeholders. You will take ownership of complex regulatory documents while combining scientific expertise, writing excellence, and project coordination skills. This position offers the opportunity to make a meaningful impact on healthcare innovation while working in a collaborative, remote environment. You will have the autonomy to lead projects, share expertise, and grow within a team focused on quality, precision, and scientific communication.

Accountabilities
  • Lead the preparation of complex clinical and regulatory documents, including Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in CTD format, Investigator Brochures, IMPDs/INDs, and scientific publications.
  • Collaborate with clinical development teams, subject matter experts, and stakeholders to produce accurate, compliant, and scientifically robust documentation.
  • Provide document-specific guidance and strategic writing support to clients and project teams.
  • Manage document timelines, review cycles, and project deliverables while ensuring quality standards and regulatory requirements are met.
  • Coordinate and oversee contributions from other medical writers, quality control specialists, and supporting team members.
  • Monitor project budgets, follow internal procedures, and ensure successful delivery within agreed timelines.
  • Work effectively within client regulatory document management systems and maintain high standards of documentation practices.
  • Act as a trusted partner throughout the clinical development process by providing expertise beyond technical writing.
Requirements
  • Several years of professional experience writing clinical regulatory documents within the pharmaceutical, biotechnology, or healthcare industry.
  • Proven experience as a lead writer for multiple regulatory document types, including at least three of the following: Clinical Study Protocols, Clinical Study Reports, CTD Clinical Summaries, Investigator Brochures, IMPDs/INDs, or scientific publications.
  • Senior-level candidates should have experience leading more than three regulatory writing projects, while Principal-level candidates should have experience leading more than five projects.
  • Principal-level experience with multiple CTD dossier types, such as new chemical entity applications, variations, generic dossiers, orphan drug dossiers, or literature-based submissions, is highly desirable.
  • Experience working directly with clients, authors, and cross-functional teams while managing review processes, meetings, and project timelines.
  • Strong understanding of regulatory documentation standards and experience using document management and review tools.
  • Bachelor's, Master's, or equivalent degree in a scientific or pharmacy-related discipline; a Ph.D. is not required.
  • Excellent written and spoken English skills with strong attention to detail and commitment to producing high-quality scientific content.
  • Strong interpersonal and communication skills, with the ability to collaborate effectively with diverse teams.
  • Ability to manage multiple priorities, remain focused under tight deadlines, and work independently in a remote environment.
Benefits
  • Fully remote work environment with flexibility within Europe.
  • Opportunity to contribute to meaningful clinical development programs in the pharmaceutical industry.
  • Competitive compensation package aligned with experience level.
  • Standard benefits package and professional development opportunities.
  • Opportunity to work with experienced medical writing professionals and international teams.
  • High level of ownership and responsibility across impactful regulatory projects.
  • Supportive environment focused on collaboration, quality, and continuous growth.
How Jobgether works:
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
 Why Apply Through Jobgether? 
 
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
 
 
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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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