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Internship Pharmd Medical Writer Jobs (NOW HIRING)

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Internship Pharmd Medical Writer information

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$38

$57

How much do internship pharmd medical writer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for internship 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 is the difference between Internship Pharmd Medical Writer vs Medical Writer?

AspectInternship Pharmd Medical WriterMedical Writer
Required CredentialsPharmD, relevant coursework, internship experienceDegree in life sciences, communications, or related field; often advanced degrees
Work EnvironmentPharmaceutical companies, biotech firms, or healthcare organizations; training-focusedMedical communication agencies, pharma companies, or publishing; more independent
Employer & Industry UsageEntry-level, training position within pharmaceutical/healthcare industryProfessional role for creating scientific content across industries

In summary, an Internship Pharmd Medical Writer is an entry-level, training-focused role for PharmD students gaining experience in medical writing within healthcare settings. A Medical Writer is a more experienced professional responsible for producing scientific content across various industries, often requiring advanced degrees and extensive experience.

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What cities are hiring for Internship Pharmd Medical Writer jobs? Cities with the most Internship Pharmd Medical Writer job openings:
What are the most commonly searched types of Pharmd Medical Writer jobs? The most popular types of Pharmd Medical Writer jobs are:
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Infographic showing various Internship 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.

Medical Writer / Clinical Document Author

micro1 AI

Bridgeport, CT • Remote

$50 - $80/hr

Part-time

Posted 4 days ago


Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.