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Remote Medical Writer Internship Jobs in California

Experience as lead writer for key documents included in major US and/or international regulatory ... San Carlos, CA or Remote Based Work Arrangement (may be adjusted based on business needs, job ...

Technical Writer Job Type: Contractor Location: Remote Job Overview We are seeking experienced ... medical devices, or regulated industries. * Strong ability to create precise, testable technical ...

Technical Writer Job Type: Contractor Location: Remote Job Overview We are seeking experienced ... medical devices, or regulated industries. * Strong ability to create precise, testable technical ...

Technical Writer Job Type: Contractor Location: Remote Job Overview We are seeking experienced ... medical devices, or regulated industries. * Strong ability to create precise, testable technical ...

Technical Writer Job Type: Contractor Location: Remote Job Overview We are seeking experienced ... medical devices, or regulated industries. * Strong ability to create precise, testable technical ...

Remote or Hybrid or Onsite Stryker is hiring a Senior Technical Writer to join our Technical ... Minimum of 2+ years of experience in technical writing within the medical device industry

Remote or Hybrid or Onsite Stryker is hiring a Senior Technical Writer to join our Technical ... Minimum of 2+ years of experience in technical writing within the medical device industry

Write clean, well-structured, and maintainable code with a strong emphasis on scalability and ... Remote-first role (US only) * ???? Medical, dental, and vision insurance * ???? 401(k) + retirement ...

Showing results 21-40

Remote Medical Writer Internship information

What is a remote medical writer internship?

A Remote Medical Writer Internship is a temporary position where interns gain experience writing and editing scientific and medical content from a remote location. Interns assist in preparing clinical documents, regulatory submissions, research articles, and educational materials under the guidance of experienced medical writers. This role helps interns develop skills in scientific communication, literature review, and understanding medical terminology. Remote internships offer flexibility, allowing interns to collaborate online with teams and clients from various locations.

What are the typical responsibilities and collaborative dynamics for a remote medical writer intern?

As a Remote Medical Writer Intern, you will typically be responsible for drafting, editing, and reviewing scientific documents such as clinical study reports, regulatory submissions, and educational materials under the guidance of senior writers. Collaboration is a key aspect, as you’ll work closely with cross-functional teams including researchers, clinicians, and regulatory specialists to ensure accuracy and compliance with industry standards. Communication is primarily conducted via digital platforms, requiring strong organizational and self-management skills. You may also participate in team meetings, receive feedback, and have opportunities for mentorship and skill development.

What are the key skills and qualifications needed to thrive as a remote medical writer intern, and why are they important?

A Remote Medical Writer Intern should have a solid background in life sciences or healthcare, strong research abilities, and excellent written communication skills, often supported by a relevant degree or coursework. Familiarity with referencing software (such as EndNote), medical databases (like PubMed), and proficiency in Microsoft Office are commonly required. Attention to detail, adaptability, and the ability to work independently are vital soft skills for excelling in remote settings. These competencies ensure accurate, clear, and compliant medical documents that effectively support healthcare communication and research objectives.

What is the difference between Remote Medical Writer Internship vs Remote Medical Writer?

AspectRemote Medical Writer InternshipRemote Medical Writer
Required CredentialsTypically pursuing or recently completed relevant degree (e.g., life sciences, healthcare)Advanced degree (e.g., Master’s, PhD) often preferred; professional experience valued
Work EnvironmentInternship setting, often part-time or temporary, with mentorshipFull-time or freelance, independent or team-based remote work
Employer & Industry UsagePharmaceutical companies, CROs, biotech firms, research institutionsPharmaceutical, biotech, medical communications agencies, CROs

The Remote Medical Writer Internship is an entry-level, temporary position designed for students or recent graduates gaining industry experience. In contrast, the Remote Medical Writer role requires more experience and often involves independent project work. Both roles are common in the pharmaceutical and biotech industries, but internships focus on training and skill development, while full-time writers handle complex documentation.

What are the most commonly searched types of Remote Medical Writer jobs in California?

The most popular types of Remote Medical Writer jobs in California are:

What cities in California are hiring for Remote Medical Writer Internship jobs?

Cities in California with the most Remote Medical Writer Internship job openings:

Infographic showing various Remote Medical Writer Internship job openings in California as of July 2026, with employment types broken down into 2% Internship, 74% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Clinical Document Author - Remote

YO AI Labs

Palo Alto, CA • Remote

$50 - $80/hr

Full-time

Posted 23 days ago


Job description

Job Title: Medical Writer / Clinical Document Author

Location: Remote
Job Type: Contractor
Pay: $50–$80/hour

Job Overview

We are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing.

Key Responsibilities
  • Author and review Clinical Study Reports (CSRs) and other regulatory documents.

  • Interpret clinical protocols and ensure compliance with ICH guidelines.

  • Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.

  • Review safety documentation, including DSURs and PSURs/PBRERs.

  • Provide structured feedback and collaborate with cross-functional teams.

  • Support AI-assisted documentation evaluation and quality improvement initiatives.

Required Skills
  • Regulatory Medical Writing

  • Clinical Study Report (CSR) Authoring

  • ICH E3 Guidelines

  • Scientific Accuracy Assessment

  • Source Data Verification

  • Clinical Protocol Interpretation

  • TFL Analysis

  • eCTD Knowledge

  • Strong Written Communication & Collaboration

Qualifications
  • 5+ years of regulatory medical writing experience in a Sponsor, CRO, or consulting environment.

  • Experience authoring Clinical Study Reports and regulatory documentation.

  • Strong knowledge of ICH E3, ICH E2F, ICH E2C, and eCTD requirements.

  • Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field (MD, PharmD, PhD, or MSc).

  • Experience in oncology and haematology is preferred.