ZipRecruiter

Log In

2

Remote Pfizer Medical Writer Jobs (NOW HIRING)

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Fully Remote (U.S.) Industry: Pharmaceutical / Biotechnology Employment Type: Full-Time Salary ... Medical Writer to support clinical development and regulatory documentation activities within a ...

Synterex

Senior Medical Writer

Boston, MA · On-site +1

... medical writing, submission publishing, and clinical science and operations support ... Synterex offers remote or on-site services, with a focus on providing clear, concise, accurate, and ...

Amiculum

Experienced medical writer - USA

Chicago, IL · On-site +1

Remote and hybrid working options as standard * Continuous learning and professional development ... Job code: CPT407 Career opportunities Medical writing Role Publications Locations USA (Remote ...

Synterex

Senior Medical Writer

Boston, MA · Remote

... medical writing, submission publishing, and clinical science and operations support ... Synterex offers remote or on-site services, with a focus on providing clear, concise, accurate, and ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

next page

Showing results 1-20

All JobsRemote Pfizer Medical Writer Jobs

Remote Pfizer Medical Writer information

See salary details

$14

$38

$57

How much do remote pfizer medical writer jobs pay per hour?

As of Jun 18, 2026, the average hourly pay for remote pfizer medical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

Is there a demand for medical writers?

There is strong demand for medical writers, especially those with expertise in regulatory, clinical, and scientific writing. The growth of the pharmaceutical and biotech industries, along with increasing regulatory requirements, drives the need for skilled medical writers who can produce accurate, compliant documentation using tools like Microsoft Word and referencing scientific data. Remote medical writing roles are also expanding, offering more opportunities for qualified professionals.

How much does a medical science liaison make at Pfizer?

A Medical Science Liaison (MSL) at Pfizer typically earns between $120,000 and $160,000 annually, depending on experience, location, and specialty. MSLs often have advanced degrees such as a PhD or PharmD and require strong scientific knowledge and communication skills.

What is the difference between Remote Pfizer Medical Writer vs Remote Medical Science Liaison?

AspectRemote Pfizer Medical WriterRemote Medical Science Liaison
Required CredentialsMedical degree or life sciences background, writing certificationsMedical or scientific degree, often with clinical or research experience
Work EnvironmentCollaborates with medical teams, writes regulatory and scientific documentsEngages with healthcare professionals, provides scientific education
Employer & Industry UsagePharmaceutical companies, biotech firms, regulatory agenciesPharmaceutical companies, medical organizations, biotech firms

Remote Pfizer Medical Writers focus on creating scientific and regulatory documents within pharmaceutical companies, while Remote Medical Science Liaisons primarily engage with healthcare professionals to communicate scientific information. Both roles require strong scientific credentials but differ in daily tasks and interactions.

Can you work from home as a medical writer?

Remote Pfizer medical writers can often work from home, as the role primarily involves writing and reviewing scientific documents, which can be done remotely with access to necessary software and data. Many companies in the industry offer flexible or fully remote positions, especially for experienced writers with strong communication and regulatory knowledge.

Does Pfizer offer remote work?

Pfizer offers remote work opportunities for many roles, including medical writers, depending on the position and team needs. Remote work arrangements may vary by department and location, and employees often use collaboration tools like virtual meetings and document sharing platforms. Candidates should review specific job postings for remote work options and requirements.
More about Remote Pfizer Medical Writer jobs
What cities are hiring for Remote Pfizer Medical Writer jobs? Cities with the most Remote Pfizer Medical Writer job openings:
What are the most commonly searched types of Pfizer Medical Writer jobs? The most popular types of Pfizer Medical Writer jobs are:
What states have the most Remote Pfizer Medical Writer jobs? States with the most job openings for Remote Pfizer Medical Writer jobs include:
What job categories do people searching Remote Pfizer Medical Writer jobs look for? The top searched job categories for Remote Pfizer Medical Writer jobs are:
Remote Pfizer Medical Writer jobs near you
Infographic showing various Remote Pfizer Medical Writer job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 42% Full Time, 54% Part Time, 2% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Senior Medical Writer

Ambition 24Hours Inc

The Lakes, NV • Remote

$142K - $195K/yr

Contractor

Posted 27 days ago

Job description

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.

───────────────────────────
Key Responsibilities
───────────────────────────
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

───────────────────────────
Requirements
───────────────────────────
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