$116K - $137K/yr
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical ...
$116K - $137K/yr
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical ...
$116K - $137K/yr
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical ...
Princeton, NJ · On-site
$116K - $137K/yr
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical ...
Princeton, NJ · On-site
$116K - $137K/yr
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical ...
$234K - $322K/yr
As the Head of Medical Writing, West Coast Hub (WCH), you will helm the functional oversight of complex development programs within Biogen's emerging nephrology and immune-mediated disease portfolio.
$234K - $322K/yr
As the Head of Medical Writing, West Coast Hub (WCH), you will helm the functional oversight of complex development programs within Biogen's emerging nephrology and immune-mediated disease portfolio.
Medical Writing Specialist Division: Strategic Medical Affairs Reports To: Medical Safety Project Manager Job Function Summary The Medical Writer Specialist is responsible for preparation of ...
Medical Writing Specialist Division: Strategic Medical Affairs Reports To: Medical Safety Project Manager Job Function Summary The Medical Writer Specialist is responsible for preparation of ...
Position: The Senior Director, Medical and Scientific Writing plays a critical role within the organization. Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in ...
Position: The Senior Director, Medical and Scientific Writing plays a critical role within the organization. Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in ...
Western Springs, IL · On-site
Strives to complete medical writing deliverables on time and within budget. * With minimal supervision, manages client expectations and interacts and communicates directly with clients, leads team ...
Western Springs, IL · On-site
Strives to complete medical writing deliverables on time and within budget. * With minimal supervision, manages client expectations and interacts and communicates directly with clients, leads team ...
Princeton, NJ · Remote
$116K - $137K/yr
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical ...
Princeton, NJ · Remote
$116K - $137K/yr
This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical ...
$128K - $176K/yr
This individual will execute the overall strategy for all medical writing processes according to argenx medical writing standards and corporate objectives. Key Accountabilities/Responsibilities:
$128K - $176K/yr
This individual will execute the overall strategy for all medical writing processes according to argenx medical writing standards and corporate objectives. Key Accountabilities/Responsibilities:
This role will provide medical writing support by organizing, analyzing, and interpreting scientific and statistical data. Such documents include all types of regulatory documents, including eCTD ...
This role will provide medical writing support by organizing, analyzing, and interpreting scientific and statistical data. Such documents include all types of regulatory documents, including eCTD ...
Position: The Senior Director, Medical and Scientific Writing plays a critical role within the organization. Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in ...
New
Position: The Senior Director, Medical and Scientific Writing plays a critical role within the organization. Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in ...
New
Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams). * Builds effective partnerships with cross-functional groups to ensure customer ...
Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams). * Builds effective partnerships with cross-functional groups to ensure customer ...
Maple Grove, MN · On-site
CER (Clinical Evaluation Review/Report) Writing * MDR (Medical Device Regulations) * EU (European Union) * Literature Review (e.g., PubMed) Responsibilities: * Write and review scientific manuscripts ...
Maple Grove, MN · On-site
CER (Clinical Evaluation Review/Report) Writing * MDR (Medical Device Regulations) * EU (European Union) * Literature Review (e.g., PubMed) Responsibilities: * Write and review scientific manuscripts ...
Education & Experience: • Minimum of a Bachelor's Degree required. • Experience in a relevant Medical Device Industry required • Minimum of 2-3 years writing experience within the Medical ...
Education & Experience: • Minimum of a Bachelor's Degree required. • Experience in a relevant Medical Device Industry required • Minimum of 2-3 years writing experience within the Medical ...
Boston, MA · On-site +1
Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead on assigned documents or identifying when external writers are necessary for ...
Boston, MA · On-site +1
Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead on assigned documents or identifying when external writers are necessary for ...
Denver, CO · Remote
$106K - $149K/yr
Develop routine, sustaining medical writing documents/deliverables; propose approaches to developing moderately complex documents/deliverables. Review and provide thoughtful feedback on moderately ...
Denver, CO · Remote
$106K - $149K/yr
Develop routine, sustaining medical writing documents/deliverables; propose approaches to developing moderately complex documents/deliverables. Review and provide thoughtful feedback on moderately ...
Irvine, CA · On-site +1
$106K - $149K/yr
Develop routine, sustaining medical writing documents/deliverables; propose approaches to developing moderately complex documents/deliverables * Review and provide thoughtful feedback on moderately ...
Irvine, CA · On-site +1
$106K - $149K/yr
Develop routine, sustaining medical writing documents/deliverables; propose approaches to developing moderately complex documents/deliverables * Review and provide thoughtful feedback on moderately ...
OR · Remote
Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments ...
OR · Remote
Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Leads the resolution of comments ...
$90K - $105K/yr
Medical Writing & Analysis * Is experienced in reviewing and developing publications for primary research results from studies involving real-world evidence, patient-reported outcomes, and health ...
New
$90K - $105K/yr
Medical Writing & Analysis * Is experienced in reviewing and developing publications for primary research results from studies involving real-world evidence, patient-reported outcomes, and health ...
New
North Billerica, MA · On-site +1
$126K - $215K/yr
Acting as the primary medical writing lead within cross-functional teams, you will define document strategy, shape submission timelines, and align stakeholders across clinical, regulatory affairs ...
North Billerica, MA · On-site +1
$126K - $215K/yr
Acting as the primary medical writing lead within cross-functional teams, you will define document strategy, shape submission timelines, and align stakeholders across clinical, regulatory affairs ...
Fort Worth, TX · On-site
Licensed healthcare professional (e.g., PharmD, PhD, RN, NP, PA) preferred but not required. * 2-5 years of experience in medical writing, Medical Information, Medical Affairs, clinical development ...
Fort Worth, TX · On-site
Licensed healthcare professional (e.g., PharmD, PhD, RN, NP, PA) preferred but not required. * 2-5 years of experience in medical writing, Medical Information, Medical Affairs, clinical development ...
$11.54 - $17.66
0% of jobs
$17.66 - $23.78
8% of jobs
$23.78 - $29.90
12% of jobs
$32.80 is the 25th percentile. Wages below this are outliers.
$29.90 - $36.01
11% of jobs
$36.01 - $42.13
11% of jobs
The median wage is $44.87 / hr.
$42.13 - $48.25
20% of jobs
$54.04 is the 75th percentile. Wages above this are outliers.
$48.25 - $54.37
15% of jobs
$54.37 - $60.49
13% of jobs
$60.49 - $66.61
7% of jobs
$66.61 - $72.73
2% of jobs
$72.73 - $78.85
2% of jobs
$11
$46
$78
| Aspect | Medical Writing | Medical Editing |
|---|---|---|
| Required Credentials | Typically requires a background in life sciences, healthcare, or related fields; often a degree or certification in medical writing | Requires strong knowledge of medical terminology and writing; often a background in healthcare, editing, or related fields |
| Work Environment | Often works independently or in teams, creating clinical documents, regulatory submissions, and educational materials | Usually works alongside writers, reviewing and refining medical documents for clarity, accuracy, and consistency |
| Employer & Industry Usage | Used in pharmaceutical, biotech, healthcare, and medical device industries | Common in publishing, healthcare communications, and regulatory agencies |
Medical Writing involves creating original medical content such as clinical study reports, regulatory documents, and educational materials. Medical Editing focuses on reviewing and refining these documents to ensure clarity, accuracy, and compliance. Both roles require strong medical knowledge, but Medical Writers produce content, while Medical Editors improve existing content.
Medical writing jobs work in health care and science communities to compose documents and articles. Those who have medical writing jobs may draft many different kinds of papers, such as educational or promotional literature, medical abstracts for textbooks, or research documents. Other medical writing jobs include ghost-writing for prominent scientists or physicians, journalistic writing for scientific magazines, or creating content for marketing materials. Regardless of what field you are in, to obtain medical writing jobs, you must be able to decipher and interpret complicated information and write in a manner that your audience understands. For example, you may use medical jargon in scientific journals, but medical writers typically use simpler language when writing for the general public.

Taiho's success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.
Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It's our work, our passion, and our legacy. We invite you to join us.
Remote Employee Value Proposition: At Taiho Oncology, the compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most. This is an exciting opportunity to experience multiple facets of medical writing in a dynamic, collaborative, and cross functional environment. Position Summary: The Senior Medical Writer, Medical Writing is accountable for the timely delivery of high quality, regulatory-compliant documents including but not limited to protocols, IBs, clinical study reports, for assigned program and ensures documents are delivered per corporate objectives, from planning through internal approval.
Performance Objectives: Responsible for the development of high-quality clinical documents submitted to Regulatory Authorities (e.g. FDA and EMA) including but not limited to Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments,. Collaborate with Global Development Teams and Clinical Development to ensure alignment with program objectives.
Participates in Global Medical Writing initiatives on clinical development cross-functional teams. Assists with development and implementation of Medical Writing processes improvement in line with SOPs. Owns and updates assigned Medical Writing SOPs, as necessary.
Education/Certification Requirements: Bachelor's Degree in life science, health-related or pharmaceutical field, or the equivalent in experience. Knowledge, Skills, and Abilities: Minimum of 3 years combined experience in academic/clinical and/or industry setting writing clinical protocols, CSRs and/or medical and/or scientific documents. Previous experience in Medical Writing in clinical drug development, preferably some experience in oncology.
Working knowledge of Medical Writing requirements and document components. Experience with templates and template development, and document management systems. Excellent writing skills.
Good interpersonal skills that involve working well in a team environment and the ability to lead others. Good organizational and planning skills; drive for results. Ability to read, analyze and interpret scientific and technical information.
Effective analytical/problem solving skills. Ability to write procedures. Ability to follow instructions and synthesize information from multiple sources.
Strong PC skills including intermediate/advanced proficiency with MS Word, and basic proficiency with other MS Office products. Adept in learning additional software utilized at Taiho. The pay range for this position at commencement of employment is expected to be between $116,450 - $137,000 annually.
This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered.
Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. #LI-Remote Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please email People@taihooncology.com . Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law.
Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records. The incumbent in this position may be required to perform other duties, as assigned. Salary: .
Date posted: 01/07/2026
Sourced by ZipRecruiter
Pharmaceutical and medicine manufacturing
201 - 500 Employees
Princeton, NJ, US
2002