The Lakes, NV · Remote
$142K - $195K/yr
Fully Remote (U.S.) Industry: Pharmaceutical / Biotechnology Employment Type: Full-Time Salary Range: $142,100 - $195,360 annually Experience Level: Mid-Senior ───── Job Overview ...
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The Lakes, NV · Remote
$142K - $195K/yr
Fully Remote (U.S.) Industry: Pharmaceutical / Biotechnology Employment Type: Full-Time Salary Range: $142,100 - $195,360 annually Experience Level: Mid-Senior ───── Job Overview ...
Yardley, PA · Remote
The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... Remote
Yardley, PA · Remote
The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... Remote
Yardley, PA · Remote
The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... Remote Employment Type: OTHER
Yardley, PA · Remote
The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... Remote Employment Type: OTHER
Yardley, PA · On-site +1
The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... Remote
Yardley, PA · On-site +1
The Senior Medical Writer will ensure high-quality content is developed for a wide range of medical ... Remote
OR · On-site +1
Senior Medical Writer (Remote) Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a ...
OR · On-site +1
Senior Medical Writer (Remote) Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a ...
Mansfield, MA · On-site +1
Title: Sr. Medical Writer Duration: 2 years Location: Mansfield, MA 02048(100% possibility of ... Remote candidates are an option. Local candidate to Mansfield, MA preferred. Essential functions:
Mansfield, MA · On-site +1
Title: Sr. Medical Writer Duration: 2 years Location: Mansfield, MA 02048(100% possibility of ... Remote candidates are an option. Local candidate to Mansfield, MA preferred. Essential functions:
The Senior Medical Writer serves as an integral part of the Real Chemistry Medical Communications division in developing scientific content in support of a variety of omnichannel medical ...
The Senior Medical Writer serves as an integral part of the Real Chemistry Medical Communications division in developing scientific content in support of a variety of omnichannel medical ...
ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of ...
ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of ...
$88K - $115K/yr
Where science meets strategy-make an impact as a Senior Medical Writer! Work shouldn't just be something we do; it should have a purpose. At Envision, we believe in creating life-changing outcomes ...
$88K - $115K/yr
Where science meets strategy-make an impact as a Senior Medical Writer! Work shouldn't just be something we do; it should have a purpose. At Envision, we believe in creating life-changing outcomes ...
$128K - $176K/yr
For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory ...
$128K - $176K/yr
For the expansion of our team, argenx is looking for a Senior Medical Writer who will provide medical writing support for developing complex clinical, nonclinical, and safety documents for regulatory ...
Boston, MA · On-site +1
$160K - $175K/yr
About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
Boston, MA · On-site +1
$160K - $175K/yr
About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of ...
ROLE: The Senior Medical Writer applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of ...
San Francisco, CA · On-site +1
$160K - $175K/yr
About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
San Francisco, CA · On-site +1
$160K - $175K/yr
About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...
$100K - $151K/yr
The Senior Medical Writer (MW) will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning ...
$100K - $151K/yr
The Senior Medical Writer (MW) will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning ...
$100K - $151K/yr
The Senior Medical Writer (MW) will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning ...
$100K - $151K/yr
The Senior Medical Writer (MW) will be responsible for leading the development of high-quality and on-time clinical study documents. Specific responsibilities include clinical document planning ...
Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across ...
Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across ...
OR · Remote
Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across ...
OR · Remote
Sr. Medical Writer (Regulatory) Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across ...
OR · On-site +1
The Opportunity This role is responsible for medical writing activities for one or more clinical development programs at Praxis, as directed by the Associate Director, Medical Writing. The individual ...
OR · On-site +1
The Opportunity This role is responsible for medical writing activities for one or more clinical development programs at Praxis, as directed by the Associate Director, Medical Writing. The individual ...
$130K - $150K/yr
The Opportunity This role is responsible for medical writing activities for one or more clinical development programs at Praxis, as directed by the Associate Director, Medical Writing. The individual ...
$130K - $150K/yr
The Opportunity This role is responsible for medical writing activities for one or more clinical development programs at Praxis, as directed by the Associate Director, Medical Writing. The individual ...
Canton, MI · On-site +1
Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...
Canton, MI · On-site +1
Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...
$35K - $54.3K
17% of jobs
$54.3K - $73.6K
0% of jobs
$73.6K - $93K
4% of jobs
$99K is the 25th percentile. Wages below this are outliers.
$93K - $112.3K
13% of jobs
$112.3K - $131.6K
13% of jobs
The median wage is $135.6K / yr.
$131.6K - $150.9K
18% of jobs
$161.3K is the 75th percentile. Wages above this are outliers.
$150.9K - $170.2K
20% of jobs
$170.2K - $189.5K
6% of jobs
$189.5K - $208.9K
5% of jobs
$208.9K - $228.2K
3% of jobs
$228.2K - $247.5K
1% of jobs
$35K
$137.3K
$247.5K
| Aspect | Remote Senior Medical Writer | Remote Medical Writer |
|---|---|---|
| Credentials | Typically requires advanced degrees (MD, PhD, PharmD) and experience | Often requires a relevant degree, such as life sciences or healthcare, with less experience needed |
| Work Environment | Works independently or leads projects, often in a collaborative team setting | Supports medical writing tasks under supervision, often in a team |
| Employer & Industry Usage | Used by pharmaceutical, biotech, and healthcare companies for complex documentation | Used across similar industries for standard medical content creation |
The main difference between a Remote Senior Medical Writer and a Remote Medical Writer lies in experience, responsibilities, and credentials. Senior Medical Writers typically have advanced degrees and more experience, handling complex projects and leading teams. Medical Writers are often earlier in their careers, focusing on supporting documentation tasks under supervision. Both roles are vital in the healthcare and pharmaceutical industries, but the senior position involves greater expertise and leadership responsibilities.
$142K - $195K/yr
Contractor
Posted 21 days ago
Senior Medical Writer – Full-Time Remote Opportunity
───────────────────────────
Location: Fully Remote (U.S.)
Industry: Pharmaceutical / Biotechnology
Employment Type: Full-Time
Salary Range: $142,100 – $195,360 annually
Experience Level: Mid-Senior
───────────────────────────
Job Overview
───────────────────────────
We are seeking an experienced Senior Medical Writer to support clinical development and regulatory documentation activities within a leading biotechnology environment. This fully remote opportunity is ideal for a highly skilled clinical science writer with extensive experience authoring Clinical Study Reports (CSRs), protocols, and regulatory submission documents across Phase I–III studies.
The ideal candidate is a hands-on writer who spends the majority of their time authoring and developing scientific and regulatory documents rather than primarily editing or managing teams. Strong expertise in clinical development, regulatory writing standards, and cross-functional collaboration is essential.
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Key Responsibilities
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Author and edit clinical study documents including protocols, protocol amendments, informed consent forms, and Clinical Study Reports (CSRs)
Prepare regulatory submission documents including briefing books and eCTD summaries/modules
Draft aggregate safety and efficacy documents including DSURs, PBRERs, and Investigator Brochures
Manage document timelines, review cycles, and comment adjudication processes
Lead and facilitate document-related meetings with cross-functional study teams
Collaborate with clinical, biostatistics, regulatory, pharmacovigilance, and data management teams
Interpret and present complex clinical data in clear scientific narratives, tables, and graphics
Ensure all documentation complies with regulatory guidelines, industry standards, and internal style guides
Support process improvements, templates, and standard operating procedures within Medical Writing
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Requirements
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Bachelor’s degree or higher in a scientific discipline required
7–10+ years of medical writing experience within biotech, pharmaceutical, or CRO environments
Extensive experience authoring Clinical Study Reports (CSRs) and protocol amendments required
Experience with INDs, NDAs, BLAs, DSURs, PBRERs, and regulatory briefing books strongly preferred
Strong understanding of clinical development processes and regulatory requirements
Experience with eCTD submissions and Modules 2–5 preferred
Ability to interpret complex clinical and statistical data
Excellent scientific writing, communication, and organizational skills
Proficiency with Microsoft Office Suite, Adobe Acrobat, Veeva, SharePoint, or similar document management systems
Ability to manage multiple projects and work independently in a remote environment
───────────────────────────
Ideal Candidate Profile
───────────────────────────
Highly experienced clinical medical writer with strong Phase I–III study expertise
Focused primarily on authoring scientific and regulatory content rather than editing or project management
Demonstrated excellence in CSR development and clinical science documentation
Biotech or pharmaceutical industry background strongly preferred
CRO experience considered
Strong attention to detail with the ability to meet strict timelines and regulatory standards
