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Drug Information Medical Writer Jobs (NOW HIRING)

Medical Writer

Princeton, NJ · On-site

$80K - $130K/yr

Position Summary The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug ...

Medical Writer

Princeton, NJ · On-site

$80K - $130K/yr

It specializes in developing innovative cancer treatments using its established drug development ... The medical writer will be responsible for the management and oversight of assigned medical writing ...

Medical Writer

Princeton, NJ · On-site

$80K - $130K/yr

It specializes in developing innovative cancer treatments using its established drug development ... The medical writer will be responsible for the management and oversight of assigned medical writing ...

Medical Writer

Bethesda, MD · On-site

$180K - $350K/yr

Are you a skilled writer with a passion for healthcare and a knack for translating complex medical information into clear, engaging content? Bethesda Family Dentistry, located in Bethesda, MD, is ...

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Medical Writer

OR · On-site +1

This role will be responsible for planning and preparing a variety of clinical and regulatory documents necessary for all phases of clinical drug development. This role will provide medical writing ...

This role will provide medical writing support by organizing, analyzing, and interpreting ... Strong understanding of drug development, clinical study design, regulations (CFR, FDA, EMA, and ...

The Medical Writer is responsible for authoring clinical trial and regulatory documents, through ... Experience understanding and interpreting data/information and its practical application. Skills ...

... information. * Qualifications Job Qualifications Education * Ph.D/Pharm D plus 1 to 2 years of related medical device/drug industry experience (e.g. medical writing, regulatory affairs, clinical ...

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Location ... drug products. This will be achieved by applying analytical skills, functional literacy and ...

Medical Writer ApotheCom, an Inizio Medical company, is an exciting leader in the field of medical ... accurate medical information for assigned projects. * Participate in client meetings ...

Medical Writer At MJH Life Sciences our success is measured by your success! If you set your ... to gather information and validate content. * Ensure compliance: Follow AMA/AP style, brand ...

... medical information. What You Will Do: You will oversee medical writing workstreams, ensuring ... deliverables meet quality and timeline expectations. Key responsibilities include: * Leading the ...

... medical information. What You Will Do: You will oversee medical writing workstreams, ensuring ... deliverables meet quality and timeline expectations. Key responsibilities include: * Leading the ...

Evidence of medical writing career development desirable, eg, American Medical Writers Association certificate, Editor in Life Sciences certificate, or relevant training through Drug Information ...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of ... information in accordance with International Council for Harmonisation (ICH) and other regulatory ...

... drug development through post-approval. Synterex is seeking an organized, motivated, and ... For more information, please visit www.synterex.com/fellowships-internships.

... drug development through post-approval. Synterex is seeking an organized, motivated, and ... For more information, please visit www.synterex.com/fellowships -internships.

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Drug Information Medical Writer information

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How much do drug information medical writer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for drug information 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 popular job titles related to Drug Information Medical Writer jobs?

For Drug Information Medical Writer jobs, the most frequently searched job titles are:

Medical Writer

Princeton, NJ • On-site

Systimmune
Biotechnology Research and Development • 1 - 10 employees

$80K - $130K/yr

Other

Re-posted 22 days ago


Job description

Located in Redmond, WA, SystImmune, Inc. is a biopharmaceutical company focused on treating cancer through developing novel therapeutic multi‑specific antibodies and antibody‑drug conjugates (ADCs).

Position Summary

The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. They will be accountable for ensuring that all documents are written according to established templates and guidance, and that they are of the highest quality with respect to scientific content, organization, accuracy, regulatory guidelines, clarity of presentation, and structure.

Key Responsibilities
  1. Write, edit and/or manage the production of high‑quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.
  2. Act as a member of clinical trial teams.
  3. Follow and track clinical documentation milestones.
  4. Write/edit other strategic documents as required.
Required Qualifications
  • 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 pharmaceutical industry.
  • Excellent writing and effective communication skills.
  • Proven interpersonal, organizational and problem‑solving skills in a matrix management environment.
  • Knowledge of FDA and ICH guidelines.
  • Skilled in clinical data interpretation.
  • Proven experience writing/supporting major documents (e.g., protocols, CSRs, ISE, ISS, and Clinical Overview).
Preferred Qualifications
  • Knowledge of drug development and regulatory requirements to guide document organization.
  • Project management experience including the use of negotiation and influence to ensure document timelines are met while maintaining high quality.

The hiring pay range for this position is $80,000 – $130,000 per year based on skills, education, and experience relevant to the role.

SystImmune offers a comprehensive benefits package.

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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