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Pharmacist Medical Writer Jobs (NOW HIRING)

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

... pharmaceuticals, medical products, and supply chain solutions to hospitals, pharmacies, and healthcare providers. The organization plays a critical role in helping healthcare systems improve ...

Up to 2 years as a medical writer in the pharmaceutical industry At least 5 years of medical or scientific writing experience as a primary job responsibility Clinical Studies Familiar with drug ...

A Medical Writer acts as a content expert, a face, and a voice for AdMed, Inc. The role involves ... Write outstanding, original scientific copy for a variety of target audiences (eg, pharmaceutical ...

Medical Writer

Manhattan, NY · On-site +1

$65K - $85K/yr

We partner with pharmaceutical, medical device, and biotech companies to drive enhanced clinical ... Writing/Content Development * Research, learn, and simplify complex scientific/medical information ...

Medical Writer

Manhattan, NY · Remote

$65K - $85K/yr

We partner with pharmaceutical, medical device, and biotech companies to drive enhanced clinical ... Writing/Content Development * Research, learn, and simplify complex scientific/medical information ...

Medical Writer

Princeton, NJ · On-site

$80K - $130K/yr

Master's degree in a life sciences discipline or at least 3 to 4 years of experience as a medical writer in the pharmaceutical industry PhD with at least 1 year experience as a medical writer in the ...

Medical Writer

Princeton, NJ · On-site

$80K - $130K/yr

Master's degree in a life sciences discipline or at least 3 to 4 years of experience as a medical writer in the pharmaceutical industry PhD with at least 1 year experience as a medical writer in the ...

Overview LabConnect improves lives by partnering with pharmaceutical and biotech companies, and ... The Medical Writer is responsible for authoring clinical trial and regulatory documents, through ...

Serves as lead Medical Writer for key programs. Coordinates medical writing support for programs ... pharmaceutical environment. Must have strong scientific and operational background. At least 3 ...

Medical Writer - Publications Nucleus Global is an international medical communications agency ... Working with leading international pharmaceutical clients, you will have the opportunity to ...

See Yourself at Telix The Medical Writer will contribute to the achievement of Telix's strategic goals by leading and driving the writing process. This role will be responsible for planning and ...

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Pharmaceutical / Biotechnology Employment Type: Full-Time Salary Range: $142,100 - $195,360 ... Medical Writer to support clinical development and regulatory documentation activities within a ...

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Pharmacist Medical Writer information

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How much do pharmacist medical writer jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for pharmacist 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.

What are the typical daily responsibilities of a pharmacist medical writer?

A Pharmacist Medical Writer is typically responsible for creating, reviewing, and editing a variety of scientific and clinical documents, such as research articles, regulatory submissions, continuing education materials, or drug monographs. Daily tasks often include analyzing clinical data, collaborating with healthcare professionals or clients, and ensuring all content aligns with current guidelines and best practices. You may also participate in team meetings, manage multiple projects simultaneously, and stay updated on the latest pharmaceutical research. This role combines research, writing, and cross-functional teamwork, providing variety and the opportunity to contribute to scientific advancement.

What are the key skills and qualifications needed to thrive as a pharmacist medical writer?

To thrive as a Pharmacist Medical Writer, you need a solid background in pharmacy or life sciences, excellent written communication skills, and experience in interpreting medical literature and clinical data. Familiarity with referencing software (such as EndNote), Microsoft Office Suite, and knowledge of regulatory writing guidelines or certifications like the Medical Writing Certification (MWC) is advantageous. Attention to detail, time management, and the ability to communicate complex information clearly are crucial soft skills for this role. These competencies ensure accuracy, compliance, and the effective communication of scientific information to varied audiences.

What is a pharmacist medical writer?

A Pharmacist Medical Writer combines expertise in pharmacy and medical communication to create scientific content for healthcare professionals, regulatory agencies, and the public. They write clinical documents, drug monographs, regulatory submissions, and educational materials, ensuring accuracy and compliance with medical guidelines. This role requires strong writing skills, attention to detail, and a solid understanding of pharmacology, therapeutic guidelines, and medical research. Pharmacist Medical Writers often work in pharmaceutical companies, medical communication agencies, or as freelancers.

What cities are hiring for Pharmacist Medical Writer jobs? Cities with the most Pharmacist Medical Writer job openings:
What are the most commonly searched types of Pharmacist Medical Writer jobs? The most popular types of Pharmacist Medical Writer jobs are:
What states have the most Pharmacist Medical Writer jobs? States with the most job openings for Pharmacist Medical Writer jobs include:
Infographic showing various Pharmacist Medical Writer job openings in the United States as of August 2026, with employment types broken down into 55% Full Time, and 45% Contract. Highlights an 55% In-person, 9% Hybrid, and 36% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Lead Medical Writer

Medasource

Dublin, OH • On-site

$80 - $90/hr

Contractor

Re-posted 17 days ago


Job description

Lead Medical Writer
Remote (must be based in EST)
Compensation: $80-$90 per hour
Contract Length: 2 month Contract to Hire (40 hours/week)
Start Date: 7/1/26
ABOUT THE ROLE
Our client is a global healthcare services and products company providing pharmaceuticals, medical products, and supply chain solutions to hospitals, pharmacies, and healthcare providers. The organization plays a critical role in helping healthcare systems improve efficiency, reduce costs, and enhance patient care through integrated distribution and data-driven solutions. As a Lead Medical Writer on a 2-month remote contract, you will autonomously author and review a range of clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and responses to health authority queries. You will contribute scientifically and strategically to submission teams, plan data analyses, review statistical analysis plans, and collaborate with cross-functional stakeholders such as Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs. This role requires advanced medical writing skills, deep knowledge of regulatory requirements, the ability to mentor junior writers, and strong interpersonal and presentation abilities. Candidates must be available to work in the Eastern Standard Time zone.
WHAT YOU'LL DO
  • Autonomously write and review clinical regulatory documents, including CTD Module II summaries, Clinical Overviews, Clinical Study Reports (CSRs), and other regulatory submissions such as responses to health authority questions, briefing books, 120-day safety updates, pediatric investigational plans, and investigator brochures
  • Contribute scientifically and strategically to submission teams at the project and/or study team level, providing input on pooling strategy, content expertise, and guidance on regulatory requirements
  • Plan and review data analyses and presentations for CSRs; review statistical analysis plans and related documents
  • Collaborate effectively with cross-functional stakeholders, including Clinical Sciences, Clinical Pharmacology, Biometry, Drug Safety, Clinical Operations, CMC, and Regulatory Affairs
  • Work with in-house Documentation Specialists to produce high-quality final documents and ensure timely delivery
  • Mentor and develop junior medical writers, providing guidance and support as needed
  • Demonstrate advanced medical writing skills and maintain up-to-date knowledge of regulatory document requirements and guidelines
  • Work independently and as part of a team, managing multiple priorities and meeting challenging deadlines
  • Exhibit excellent interpersonal and presentation skills in all interactions
  • Maintain advanced proficiency in English for all written and verbal communications
WHAT YOU BRING
  • Advanced degree in life sciences (PhD, PharmD, MD, or MS preferred)
  • 5+ years of regulatory/medical writing experience in the pharmaceutical industry across several therapeutic areas
  • Proven ability to autonomously write and review clinical regulatory documents (e.g., CTD Module II summaries, CSRs, Clinical Overviews, Investigator brochures, and other regulatory submissions)
  • Strong knowledge of regulatory document requirements and guidelines
  • Experience contributing scientifically and strategically to submission teams
  • Ability to plan data analyses and review statistical analysis plans for CSRs
  • Excellent collaboration skills with cross-functional stakeholders
  • Well-developed medical writing skills with attention to quality and deadlines
  • Ability to mentor and develop junior medical writers
  • Ability to work independently and as part of a team
  • Strong interpersonal and presentation skills
  • Advanced level of English proficiency
  • Ability to work under pressure and meet challenging deadlines
  • Remote work capability with availability in Eastern Standard Time (EST)