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Remote Medical Writer Intern Jobs (NOW HIRING)

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 ...

New

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 ...

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 ...

... 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 ...

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 ...

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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Remote Medical Writer Intern information

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$46

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

As of Jun 12, 2026, the average hourly pay for remote medical writer intern in the United States is $46.27, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $56.01 per hour, depending on experience, location, and employer.

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

AspectRemote Medical Writer InternRemote Medical Writer
CredentialsTypically pursuing or recently completed relevant degree (e.g., life sciences, medicine)Usually holds advanced degrees (e.g., PhD, MD) or equivalent experience
Work EnvironmentInternship setting, often part-time or temporary, with mentorshipFull-time, professional role with independent responsibilities
Industry UsageEntry-level position for training and skill developmentEstablished role for creating scientific and medical content
Search & Comparison IntentUnderstanding entry-level opportunities and training rolesLooking for professional medical writing positions

The main difference between a Remote Medical Writer Intern and a Remote Medical Writer is experience and responsibility. Interns are typically students or recent graduates gaining initial exposure, while medical writers are experienced professionals producing scientific content independently.

What are common challenges faced by Remote Medical Writer Interns and how can they be addressed?

Remote Medical Writer Interns often face challenges such as managing time effectively, communicating clearly with cross-functional teams, and adapting to complex medical terminology. To address these, interns should establish a structured daily routine, proactively seek feedback from mentors, and utilize available reference materials to deepen their subject knowledge. Regular virtual check-ins with supervisors and team members also help maintain alignment and foster collaboration, even when working remotely.

What does a Remote Medical Writer Intern do?

A Remote Medical Writer Intern assists in creating scientific documents, articles, and reports related to medical and healthcare topics, often under the supervision of experienced writers or editors. Their tasks may include conducting literature reviews, summarizing clinical data, editing manuscripts, and ensuring content accuracy and compliance with industry standards. Working remotely, they collaborate with team members via digital platforms, gaining hands-on experience with real-world medical writing projects. This role is ideal for students or recent graduates interested in medical communications or healthcare publishing.

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

To thrive as a Remote Medical Writer Intern, you need strong writing skills, a solid understanding of medical terminology, and typically a background or coursework in life sciences or healthcare. Familiarity with reference management software, Microsoft Office Suite, and sometimes basic knowledge of regulatory guidelines is important. Attention to detail, time management, and the ability to communicate complex information clearly are essential soft skills. These qualities ensure the intern can produce accurate, high-quality medical documents that meet industry standards and deadlines while working independently.
More about Remote Medical Writer Intern jobs
What cities are hiring for Remote Medical Writer Intern jobs? Cities with the most Remote Medical Writer Intern job openings:
What are the most commonly searched types of Remote Medical Writer jobs? The most popular types of Remote Medical Writer jobs are:
What states have the most Remote Medical Writer Intern jobs? States with the most job openings for Remote Medical Writer Intern jobs include:
Infographic showing various Remote Medical Writer Intern job openings in the United States as of June 2026, with employment types broken down into 93% Full Time, and 7% Part Time. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.
Medical Writer - India (56829)

Medical Writer - India (56829)

Praxis Precision Medicines, Inc

Boston, MA • On-site, Remote

Contractor

Posted 11 days ago


Job description

Praxis is seeing a Medical Writer who will work under the guidance of the Associate Director, Medical Writing and will help support the needs of one or more clinical development programs at Praxis. You will be responsible for completing accurate, high quality, and regulatory compliant documents in support of clinical trials and regulatory submissions. This requires the knowledge and expertise to collaboratively author required documents with support and input from the Associate Director, Medical Writing while also helping other teams follow medical writing processes and style requirements. This position will be remote and located in India.
Primary Responsibilities
  • Implements all activities related to the preparation of defined medical and regulatory documents, serving as writing lead on assigned documents or identifying when external writers are necessary for support
  • Supports documents for regulatory submissions to US and global health authorities, including Investigational New Drug (IND) applications, New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), protocols, investigator brochures, clinical study reports, briefing documents, regulatory responses to health authority questions, and scheduled reports.
  • Collaborates with cross-functional team members, eg, Clinical Pharmacology, Toxicology, Research, Clinical Development, Regulatory Affairs, Biostats, Data Management, Quality, CMC, QC, etc., to ensure accurate and timely completion and delivery of high-quality, scientifically-sound documents, slide decks, and publications
  • Supports clinical trial transparency and disclosures, including clinical trials registration and results posting on clinicaltrials.gov, EudraCT, and similar databases worldwide
  • Contributes to departmental development through editorial and review support for document templates, style standards, reviewer guidelines, and standard operating procedures to ensure consistent and high-quality deliverables
  • Ensures adherence to relevant SOPs and internal best practices

Qualifications and Key Success Factors
  • Bachelor's degree required within a scientific discipline. Advanced degree, CNS, and Rare Disease experience a plus.
  • A minimum of 3 years of medical writing experience in Sponsor or CRO setting
  • AMWA certification preferred
  • Experience using medical writing systems and technologies including Veeva RIM
  • Knowledge of drug development, study conduct processes, ICH guidelines, and FDA/EU guidance or demonstrated success within a regulated industry environment
  • Represents the core Praxis values of Trust, Ownership, Curiosity, and Results
  • Ability to think critically in a fast-paced environment with a keen sense of urgency and demonstrated ability in creating solutions
  • Self-motivated, able to work autonomously, and able to be a key contributor to one or more high-functioning and collaborative teams
  • Highly organized and detail-oriented with a passion to deliver quality results quickly
  • Strong verbal and written communication skills with an ability to build relationships internally and externally
  • Highest levels of professionalism, confidence, personal values, and ethical standards

Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
Attention: Job Scam Alert
Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to careers@praxismedicines.com.
Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.