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Study Guide Writer Jobs (NOW HIRING)

BeiGene, Inc.

Principal Medical Writer

$119K - $159K/yr

Document Writing: * Manages the assigned writing tasks and ensures that the documents adhere to ... Understands the global MW scope and works to guide study team(s) and program team(s) within the ...

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

... III studies. The ideal candidate is a hands-on writer who spends the majority of their time ... and internal style guides Support process improvements, templates, and standard operating ...

Telix Pharmaceuticals (AMER)

OR

... study protocol synopses and protocols, Investigator Brochures, patient safety narratives, and ... Develop and update pertinent SOPs, processes, templates, style guides, and manuals, as needed.

Boulder Crest

Instructor (PATHH Guide)

Sonoita, AZ · On-site

Boulder Crest is the global leader in the development, delivery, study, and scale of Posttraumatic ... Good Communicator in both written and oral forms. Must be able to communicate (in the English ...

MMS

Senior Medical Writer (Remote)

Canton, MI · On-site

... study design, statistical significance, scientific rigor and absence of bias * Write and edit ... Expert proficiency with client templates & style guides * Interact directly and independently with ...

MMS

Senior Medical Writer (Remote)

Phoenix, AZ · On-site

... study design, statistical significance, scientific rigor and absence of bias * Write and edit ... Expert proficiency with client templates & style guides * Interact directly and independently with ...

Kforce Technology Staffing

IT Tech Writer

Miramar, FL

... guides, and other materials for our IT products and services. They will work closely with our ... Bachelor's degree in appropriate field of study or equivalent work experience required * 1-3 years ...

Huck Adventures

Legal Consultant & Writer

Boulder, CO · On-site

Created by Outfits and guides in Colorado. Otter Waiver's powerful features were built to save you ... We are wanting to have two articles written each month in those topics including case studies to ...

Huck Adventures

Legal Consultant & Writer

Boulder, CO · On-site

Created by Outfits and guides in Colorado. Otter Waiver's powerful features were built to save you ... We are wanting to have two articles written each month in those topics including case studies to ...

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Study Guide Writer information

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$42K

$78.9K

$136K

How much do study guide writer jobs pay per year?

As of Jun 8, 2026, the average yearly pay for study guide writer in the United States is $78,865.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $102,000.00 per year, depending on experience, location, and employer.

What does a typical day look like for a Study Guide Writer?

As a Study Guide Writer, your day often involves researching educational topics, drafting new content, editing existing material for clarity and accuracy, and collaborating with subject matter experts or editorial teams. You may also review feedback from users or educators to continuously improve your guides. The role requires balancing independent writing with regular communication and collaboration to ensure the material aligns with curriculum standards and learning objectives. Depending on the employer, work can be remote, in-office, or a mix, and deadlines are common due to publishing schedules.

What are the key skills and qualifications needed to thrive in the Study Guide Writer position, and why are they important?

To thrive as a Study Guide Writer, strong research abilities, clear and concise writing skills, subject matter expertise, and a background in education or publishing are essential. Familiarity with digital editing tools, style guides (such as APA or MLA), and content management systems is typically expected. Creativity, attention to detail, and the ability to simplify complex information are valuable soft skills in this role. These competencies ensure that study guides are accurate, engaging, and accessible to learners, meeting the needs of both students and educational institutions.

What is a Study Guide Writer job?

A Study Guide Writer creates summaries, analyses, and educational content to help students or readers understand complex subjects. They break down key concepts, themes, and important details in a clear and structured format. These guides are often used for academic study, exam preparation, or book analysis. Writers may work for educational publishers, online learning platforms, or freelance. The goal is to enhance comprehension and retention of the material.

More about Study Guide Writer jobs
What cities are hiring for Study Guide Writer jobs? Cities with the most Study Guide Writer job openings:
What states have the most Study Guide Writer jobs? States with the most job openings for Study Guide Writer jobs include:
What job categories do people searching Study Guide Writer jobs look for? The top searched job categories for Study Guide Writer jobs are:
Study Guide Writer jobs near you
Infographic showing various Study Guide Writer job openings in the United States as of May 2026, with employment types broken down into 81% Full Time, and 19% Part Time. Highlights an 100% In-person job distribution, with an average salary of $78,865 per year, or $37.9 per hour.
Principal Medical Writer

Principal Medical Writer

BeiGene, Inc.

Remote

$119K - $159K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
This position is responsible for providing expertise to support the development of high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and life-cycle management of products in BeiGene pipeline. The clinical and regulatory documents include, but are not limited to, clinical study protocols, investigator brochures, clinical study reports, regulatory briefing documents, and clinical modules of INDs, NDAs, BLAs, MAAs and other regulatory submissions. This position is also responsible for mentoring junior MWs (full-time employees and/or contractors/vendors) as needed.
Essential Functions of the Job:
Document Writing:
  • Manages the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as BeiGene SOP/WI(s), template(s), and style guide.

  • Be able to manage multiple documents at the same time, including the complex documents (eg, those with complex content, urgent timeline, or external collaboration). Leads direction and strategy setting (including critically analyzing, synthesizing, and presenting complex information) for document development in collaboration with study team(s), and be able to help other MWs as requested.

  • Contributes to the creation of document writing template/guidance for the document types listed in the General Description part. Leads part of the maintenance of document writing template/guidance for the document types listed in the General Description part.

Project /Program Management:
  • Navigates through uncertainties to develop and manage timeline of individual documents and multiple documents (supported by different MWs in one project, eg, works as the MW filing lead for an NDA/BLA/MAA submission). Be able to help other MWs as requested.

  • Be able to identify the questions/issues that require departmental discussion or team discussion. Be able to identify the potential risks, make a mitigation plan, and work to resolve problems. Be able to help other MWs in these areas as requested.

  • Builds relationship with study team(s) and program team(s) (eg, works as the MW program lead).

  • Understands the role of own documents within the larger dossier and voices out any impact on upstream and downstream processes. Be able to help other MWs as requested.

Process/Tool Establishment and Optimization:
  • Proactively identifies needs for process/tool optimization and establishment, and proposes solutions.

  • Leads part of departmental process/tool optimization. Contributes to departmental process/tool establishment.

  • Contributes to cross-functional and cross-company process/tool optimization.

Training and Mentoring:
  • Leads (part of) the development of new training programs. Provides instructions/trainings (content-wise/process-wise) to junior MWs.

  • Provides technical and operational mentorship to junior MWs (full-time employees and/or contractors/vendors).

Influence:
  • Understands the global MW scope and works to guide study team(s) and program team(s) within the defined scope and responsibility following established processes.

  • Provides topic sharing on regulatory writing and related knowledge within the department (and to cross-functional stakeholders with guidance from line manager/mentor).

  • Provides topic sharing on regulatory writing and related knowledge across companies (eg, meetings of DIA and medical writing communities) with guidance from line manager/mentor.

Supervisory Responsibilities:
  • None.

Education Required:
An advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science is preferred.
Bachelor's with 5+, MS with a minimum of 4+ years of regulatory document writing (or equivalent) experience, or PhD/PharmD/MD with a minimum of 2+ years of regulatory document writing (or equivalent) experience.
Computer Skills:
Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems; proficiency in Microsoft Outlook, Excel, and PowerPoint, etc.
Travel:
On occasion, as needed.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $119,300.00 - $159,300.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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