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Remote Science Writer Internship Jobs in California

The Borgen Project

Writer/Journalist Internship: The role is focused on content creation for BORGEN Magazine or The Borgen Project Blog. This is a part-time 12-hours per week, 12 week, unpaid remote internship. If your ...

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Remote Science Writer Internship information

What is the difference between Remote Science Writer Internship vs Remote Science Content Coordinator?

AspectRemote Science Writer InternshipRemote Science Content Coordinator
Required CredentialsRelevant science degree or coursework, writing samplesSimilar credentials, often with additional project management skills
Work EnvironmentRemote, internship setting, entry-levelRemote, coordinating content teams, more experienced
Employer & Industry UsageResearch institutions, science media, publishingScientific organizations, media outlets, educational platforms
Search & Comparison IntentEntry-level science writing roles, internshipsContent management, team coordination roles

The Remote Science Writer Internship focuses on developing writing skills in a remote setting for those starting their science communication careers. In contrast, the Remote Science Content Coordinator involves managing and coordinating content creation, requiring more experience. Both roles are remote and industry-specific, but they differ in responsibilities and career level.

What is a Remote Science Writer Internship?

A Remote Science Writer Internship is a position where interns work from home or another remote location to create, edit, and review science-related content. Interns may write articles, summaries, reports, or social media posts about scientific topics, often translating complex research into accessible language for a wider audience. This type of internship offers valuable experience in scientific communication, research, and writing, and is typically suited for students or recent graduates with a background in science and an interest in journalism or science communication.

What are the key skills and qualifications needed to thrive as a Remote Science Writer Intern, and why are they important?

To thrive as a Remote Science Writer Intern, you need strong writing, research, and analytical skills, often supported by a background in science or journalism. Familiarity with citation styles, scientific databases, and content management systems is typically required. Exceptional communication, attention to detail, and time management are crucial soft skills for standing out in this role. These skills ensure accurate, engaging, and timely science communication to a broad audience in a remote work environment.

What are some common challenges faced by remote science writer interns, and how can they be addressed?

Remote science writer interns often face challenges such as managing time effectively across different projects, staying motivated without in-person supervision, and ensuring clear communication with editors and team members. To overcome these, it's helpful to establish a structured daily routine, set clear deadlines, and utilize collaboration tools like Slack or Trello for regular updates. Additionally, proactively seeking feedback and participating in virtual meetings can foster connection and support professional growth.
What are popular job titles related to Remote Science Writer Internship jobs in California? For Remote Science Writer Internship jobs in California, the most frequently searched job titles are:
What job categories do people searching Remote Science Writer Internship jobs in California look for? The top searched job categories for Remote Science Writer Internship jobs in California are:
What cities in California are hiring for Remote Science Writer Internship jobs? Cities in California with the most Remote Science Writer Internship job openings:
Remote Science Writer Internship jobs near you

Associate Director, Medical Writer

MannKind Corporation

Westlake Village, CA • On-site, Remote

$148K - $222K/yr

Full-time

Posted 4 days ago

Job description

MannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions, developing and commercializing innovative inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases. The company applies deep expertise in formulation science and inhalation‑device engineering to reduce the treatment burden for conditions such as diabetes, congestive heart failure, pulmonary fibrosis, and pulmonary hypertension.

MannKind’s core technologies, including ultrafine dry‑powder formulations and advanced inhalation platforms, enable rapid, convenient delivery of medicines directly to the deep lung. This approach supports both local pulmonary targeting and systemic delivery for various medical indications. Through alternative drug formulations and delivery mechanisms, MannKind aims to bring forward differentiated, patient‑centric therapies that expand treatment options to improve outcomes across chronic and rare diseases.
At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Position Summary:
MannKind Corporation is seeking a detail-oriented and highly organized Medical Writer to join our team. The Medical Writer will provide advanced scientific writing expertise and ensure the successful preparation of high-quality documents including but not limited to study protocols, CSRs, DSURS, IB, safety narratives, publications and submission documents. This role involves providing medical writing support for multiple compounds and projects within multiple therapeutic areas, potentially interfacing with external groups, and serving as the scientific writing expert for the department.
Essential Duties and Job Functions:
  • Coordinate and lead the review, approval, and production of writing projects, arranging and driving review meetings with cross-functional teams.
  • Ensure effective communication among project team members and contributors, holding them accountable to agreed-upon project dates.
  • Leads strategic document preparation for INDs, NDAs and briefing documents
  • Establish best practices, workflow infrastructure/templates, and standards to enhance consistency and quality across all regulatory and scientific documents.
  • Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.
  • Stay abreast of global regulatory requirements and guidelines (FDA, EMA, PMDA, ICH, etc.), ensuring company compliance and best practices.
  • Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing.
  • Lead and oversee medical writing project timelines, ensuring alignment with broader corporate milestones.
  • Serve as the medical writer representative on project teams.
  • Write and edit scientific, clinical, or abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives.
  • Complete reviews, quality checks and approvals.
  • Summarize results presented in graphical, tabular, and/or listing format.
  • Interpret complex clinical data and convert it into clear, concise, and engaging scientific content for diverse audiences.
Knowledge, Experience and Skills:
  • BS/BA +12 / MS/MBA 8-10, PhD 5+
  • Degree in science or medical related field. Master’s or PhD preferred.
  • Minimum of 7 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R amp;D.
  • Knowledge of US and international regulations, requirements, and guidance associated with writing projects.
  • Excellent written and oral communication skills, attention to detail, and ability to correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy.
  • Extensive experience working with collaborative, cross-functional teams
  • Develop and/or update document templates, work instructions, style guides, and department-related processes (SOPs)
  • Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred.
  • Understanding of publication/scientific communication guidelines.
  • Ability to provide strategic oversight while managing multiple priorities in a fast-paced environment.
  • Deep understanding of ICH-GCP guidelines and other relevant regulatory requirements.
  • Strategic thinker with strong execution skills.
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