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Pharmd Medical Writer Jobs (NOW HIRING)

MJH Life Sciences

Principal Medical Writer

Cranbury, NJ · On-site

$95K - $105K/yr

The Principal Medical Writer is responsible for the development and quality of medical content for ... Advanced degree (MD, DO, PharmD, PhD, MS) in a healthcare-related field (life sciences, biomedical ...

MJH Life Sciences

Principal Medical Writer

Cranbury, NJ · On-site

Advanced degree (MD, DO, PharmD, PhD, or MS) in a healthcare-related field including life sciences ... medical writing or scientific communications work. This includes: * Specific tools in active use ...

Real Chemistry

Senior Medical Writer

The Senior Medical Writer serves as an integral part of the Real Chemistry Medical Communications ... Advanced degree (eg, MD, PhD, PharmD, MPH, MS) in a healthcare-related field required * Minimum of ...

GlaxoSmithKline

Principal Medical Writer

Durham, NC · Remote

Advanced degree (e.g., PhD, PharmD, MPH, MS) in life sciences or a related field. * Experience ... Medical Writing, Pharmaceutical Industry, Presentation Techniques, Regulatory Submissions ...

BeiGene, Inc.

Principal Medical Writer

$119K - $159K/yr

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 ...

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How much do pharmd medical writer jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for pharmd 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 key skills and qualifications needed to thrive as a PharmD medical writer, and why are they important?

To thrive as a PharmD Medical Writer, you need a doctorate in pharmacy (PharmD), strong scientific writing skills, and deep knowledge of medical terminology and drug development. Familiarity with reference management software, publication guidelines (such as ICMJE, GPP), and regulatory documentation tools like Microsoft Word and EndNote is typically required. Exceptional attention to detail, time management, and effective communication skills help you stand out in this collaborative and fast-paced field. These skills are essential to ensure accuracy, compliance, and clarity in producing high-quality medical documents for various stakeholders.

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

As a PharmD Medical Writer, your typical day may involve drafting, editing, and reviewing a range of scientific documents, such as clinical study reports, regulatory submissions, and peer-reviewed manuscripts. You often collaborate with clinical teams, scientists, and regulatory affairs professionals to ensure scientific accuracy and clarity in all materials. Additionally, you may participate in literature reviews, data analysis, and respond to feedback from clients or subject matter experts. There is a strong emphasis on meeting deadlines and maintaining compliance with industry standards and guidelines throughout your writing projects.

What is a PharmD medical writer?

A PharmD Medical Writer is a professional with a Doctor of Pharmacy (PharmD) degree who specializes in creating scientific and medical content. They translate complex pharmaceutical and clinical information into clear and accurate documents for healthcare professionals, regulatory agencies, or the general public. Their work may include writing clinical study reports, regulatory submissions, drug monographs, medical education materials, and promotional content. Strong research skills, knowledge of medical terminology, and the ability to communicate complex information effectively are essential. These writers often work for pharmaceutical companies, medical communication agencies, or as freelancers.

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Pharmd Medical Writer jobs near you
Infographic showing various Pharmd Medical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

Principal Medical Writer

MJH Life Sciences

Cranbury, NJ • On-site

$95K - $105K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 29 days ago

Job description

At MJH Life Sciences our success is measured by your success! If you set your standards high and want to contribute to a winning team, we'll provide you with every opportunity to help grow our company and your career. Our associates come from all backgrounds, sharing one key quality: determination to succeed. We value being Service Focused, having a Passion for Winning, Innovation, Respect, Integrity, and Teamwork. Nothing means more to us than hiring people with these attributes. If you believe you're right for the job, this is the place to prove it!
Position Overview: The Principal Medical Writer is responsible for the development and quality of medical content for publication to meet the educational needs of audiences across a range of therapeutic fields. In addition to representing the Clinical Communications team as a content expert, the Principal Medical Writer interfaces with clients, promotional review teams, key opinion leaders, and a variety of internal professional services. Candidates must demonstrate superior communication skills as well as the ability to adapt quickly and multitask to meet deadlines, ensuring content produced meets high standards of quality, accuracy, and relevance for audiences.
Key Responsibilities:
  • Content Development:
    • Develop high-quality scientific content for print and event deliverables targeted toward healthcare professionals that is aligned with the strategic objectives of the activity.
    • Perform extensive literature reviews on various disease states, therapeutic advancements, and clinical data.
    • Adhere to appropriate reference and annotation standards and resolving fact-check queries, ensuring clinical accuracy of all content.
    • Review and edit content at multiple stages for consistency, accuracy, relevance, and adherence to style guidelines.
    • Independently address and incorporate feedback from clients, peer reviewers, and/or faculty authors throughout the content development process.

  • Collaboration and Communication:
    • Work closely with cross-functional teams, communicating effectively with cross-functional stakeholders, clients, and key opinion leaders.
    • Assign tasks to internal writers and freelancers, managing workflow and reassigning tasks as needed.
    • Collaborate with project management and creative services to ensure that revisions and appropriate changes are addressed within the scope of the project.

  • Compliance and Review Process:
    • Prepare materials for pharmaceutical promotional review processes, ensuring compliance with submission requirements.
    • Revise content as needed through its internal and external reviews during the project lifecycle, adhering to medical/legal/regulatory (MLR) review process requirements.

  • Medical Event Attendance:
    • Attend live events such as consensus meetings and professional conferences to capture key content for project deliverables.
    • Produce high-quality executive summaries and/or manuscripts based on event coverage.

  • Management and Mentorship:
    • Support and train direct reports to independently accomplish all essential roles and responsibilities described above. This will require supplying accurate precise directives for each assignment, review and guidance in best practices of writing/editing,
    • Provide training and mentorship to junior Medical Writers and Editors, offering guidance on best practices in medical writing and editing.
    • Assist writers/editors on the team in workload prioritization with deliverables and timelines of projects, prioritizing timely delivery of high-quality content.

Qualifications:
  • Advanced degree (MD, DO, PharmD, PhD, MS) in a healthcare-related field (life sciences, biomedical sciences) preferred.
  • Minimum of 3 years experience at a medical communications agency or company.
  • Superior verbal and written communication skills.
  • Ability to multitask, manage multiple timelines, and solve problems effectively.
  • Proficiency in AMA style and in-house editorial standards.
  • Travel: Ability to travel for events/meetings (1-3 days quarterly on average).

Compensation Range:
$95,000 - $105,000 per year, depending on qualifications. Eligible for annual company bonus program or commission incentive based on role. The compensation offered to the candidate selected for this position will depend on several factors, including the candidate's educational background, skills, and professional experience.
Benefits Overview:
We're proud to offer a comprehensive benefits package, including:
  • Hybrid work schedule
  • Health insurance through Cigna (medical & dental)
  • Vision coverage through VSP
  • Pharmacy benefits through OptumRx
  • FSA, HSA, Dependent Care FSA, and Limited Purpose FSA options
  • 401(k) and Roth 401(k) with company match
  • Pet discount program with PetAssure
  • Norton LifeLock identity theft protection
  • Employee Assistance Program (EAP) through NYLGBS
  • Fertility benefits through Progyny
  • Commuter benefits
  • Company-paid Short-Term and Long-Term Disability
  • Voluntary Term Life & AD&D Insurance, plus Universal Life Insurance options
  • Supplemental Aflac coverage: Accident, Critical Illness, and Hospital Indemnity
  • Discounts and rewards through BenefitHub

#LI-Remote
MJH Life Sciences provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. All employees of MJH Life Sciences are employed "At Will." This means that either the employee or the Company is free to end the employment relationship at any time, for any reason, with or without cause and with or without notice.

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