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Remote Teen Medical Writer Jobs (NOW HIRING)

ViiV Healthcare

Principal Medical Writer

Durham, NC · On-site +1

ViiV Healthcare is seeking a Principal Medical Writer who will lead and deliver high-quality ... Experience working in multicultural or remote team settings. * Proven ability to independently ...

Olema Oncology

Lead Senior Medical Writer

Boston, MA · On-site +1

$160K - $175K/yr

About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

Olema Oncology

Lead Senior Medical Writer

San Francisco, CA · On-site +1

$160K - $175K/yr

About the Role >>> Lead Senior Medical Writer As the Lead Senior Medical Writer, reporting to the ... Experience working in hybrid/remote environments Attributes: * Teamwork and collaboration; balances ...

Brightside Health

Teen Therapist - Telehealth

$83 - $95/hr

Remote Teen Therapist (LCSW, LPC, LMFT)-1099 Contractor | Telehealth Join Brightside Health as a ... Enjoy our easy-to-use electronic medical record (EMR) integrated with treatment software ...

Trilogy

Senior/Principal Medical Writer - USA

Durham, NC · On-site +1

$120K - $159K/yr

... remote) from our Durham, NC, USA office. You willbe responsible for: * Preparinga variety of ... As a Senior/Principal Medical Writer, you will: * Function as a lead writer to prepare a variety of ...

Jj

Medical Writer II, Oncology

Titusville, NJ · On-site +1

Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose: * Develops within the medical writing role within the pharmaceutical industry. * Works in a team ...

Jj

Medical Writer II, Oncology

Spring House, PA · On-site +1

Remote work options may be considered on a case-by-case basis and if approved by the Company. Purpose: * Develops within the medical writing role within the pharmaceutical industry. * Works in a team ...

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How much do remote teen medical writer jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for remote teen 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.
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Remote Teen Medical Writer jobs near you

Associate Director, Medical Writer

MannKind Corporation

Westlake Village, CA • On-site, Remote

$148K - $222K/yr

Full-time

Posted yesterday

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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