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Medical Writing Fellowship Jobs (NOW HIRING)

Senior Medical Writer

Princeton, NJ ยท On-site

$110 - $160/hr

Synterexisseekingan organized, motivated, and collaborative individual for our medical writing team ... For more information, please visit www.synterex.com/fellowships-internships. #J-18808-Ljbffr

Senior Medical Writer

Princeton, NJ ยท On-site

$120K/yr

Synterex is seeking an organized, motivated, and collaborative individual for our medical writing ... For more information, please visit www.synterex.com/fellowships-internships.

Senior Principal Medical Writer

Billerica, MA ยท On-site

$126K - $215K/yr

Acting as the primary medical writing lead within cross-functional teams, you will define document ... Beyond your individual contributions, you will mentor and develop fellow writers, champion best ...

Synterex is seeking an organized, motivated, and collaborative individual for our medical writing ... For more information, please visit www.synterex.com/fellowships -internships.

Synterexisseekingan organized, motivated, and collaborative individual for our medical writing team ... For more information, please visit www.synterex.com/fellowships-internships.

Synterexisseekingan organized, motivated, and collaborative individual for our medical writing team ... For more information, please visit www.synterex.com/fellowships-internships.

The fellow's role includes formal didactics, oversight of study design and implementation, and mentorship in medical writing. 6. Serve as a research mentor to Masters level students from the School ...

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Medical Writing Fellowship information

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$11

$46

$78

How much do medical writing fellowship jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for medical writing fellowship 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 a medical writing fellowship?

A Medical Writing Fellowship is a structured training program designed to provide early-career professionals with hands-on experience in medical writing. Fellows typically work under the guidance of experienced writers and editors, learning to create regulatory documents, clinical study reports, manuscripts, and other scientific materials. These fellowships often last 1-2 years and offer mentorship, networking opportunities, and exposure to various therapeutic areas. The goal is to prepare participants for a successful career in medical writing within the pharmaceutical, biotechnology, or healthcare communication industries.

What types of projects can a medical writing fellow expect to work on during the fellowship, and how does this experience support future career growth?

As a Medical Writing Fellow, you can expect to engage in a variety of projects such as drafting clinical study reports, preparing regulatory submission documents, developing manuscripts for publication, and creating educational materials for healthcare professionals. These experiences provide hands-on exposure to different medical writing formats and therapeutic areas, helping you build a diverse portfolio. Collaborating closely with cross-functional teams like clinical researchers, regulatory affairs, and subject matter experts also hones your communication and project management skills. This multifaceted exposure is highly valued by employers and sets a strong foundation for advancement into senior medical writing or leadership roles.

What are the key skills and qualifications needed to thrive as a medical writing fellow, and why are they important?

To thrive as a Medical Writing Fellow, you need a strong background in life sciences or medicine, excellent writing skills, and a keen attention to detail, often supported by an advanced degree such as a PhD, PharmD, or MD. Familiarity with referencing software (like EndNote), document management systems, and knowledge of regulatory guidelines (such as ICH or GPP) are typically required. Outstanding communication, time management, and adaptability are crucial soft skills in this position. These skills ensure the accurate, clear, and timely delivery of complex scientific information for regulatory, educational, or publication purposes.

What is the difference between Medical Writing Fellowship vs Medical Writer?

AspectMedical Writing FellowshipMedical Writer
CredentialsTypically requires a degree in life sciences or related field; some fellowships may require prior writing experienceRequires a degree in life sciences, healthcare, or related field; certification is optional but beneficial
Work EnvironmentOften in academic, pharmaceutical, or biotech settings; focused on training and mentorshipIn-house or freelance; involved in producing clinical, regulatory, or marketing documents
Industry UsageUsed as a training program for aspiring medical writersProfessional role for experienced or entry-level writers in healthcare and pharma

In summary, a Medical Writing Fellowship is a training program designed to develop skills in aspiring medical writers, often within academic or industry settings. A Medical Writer is a professional who produces scientific and regulatory documents, with varying levels of experience. Fellowships serve as a stepping stone into the medical writing profession, whereas medical writers are actively engaged in document creation across healthcare sectors.

Do medical writers make good money?

Medical writers typically earn competitive salaries that vary based on experience, education, and location. Entry-level positions may start around $60,000 annually, while experienced professionals or those with specialized skills can earn over $100,000 per year. The role often requires strong writing skills, knowledge of medical terminology, and familiarity with regulatory guidelines.

How can I get into a medical writing fellowship with no experience?

Medical writing fellowships often accept candidates with strong scientific backgrounds, such as degrees in life sciences or related fields, even without prior experience. Gaining skills in scientific communication, familiarity with medical terminology, and proficiency in tools like Microsoft Word or reference management software can improve your chances; completing relevant courses or certifications can also be beneficial.

Is there a demand for medical writing fellows?

There is a growing demand for medical writing fellows as the healthcare and pharmaceutical industries require skilled professionals to create clinical, regulatory, and scientific documentation. These roles often require strong writing skills, knowledge of medical terminology, and familiarity with industry regulations, making them valuable in the healthcare communication field.
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The top searched job categories for Medical Writing Fellowship jobs are:

Infographic showing various Medical Writing Fellowship job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Senior Medical Writer

Synterex, Inc.

Princeton, NJ โ€ข On-site

$110 - $160/hr

Other

Posted 12 days ago


Job description

Job Description

Synterex, Inc. is aglobalconsortium of highly experienced clinical development professionals specializing in medical writing, submission publishing, and clinical science and operations support.Synterexoffers remote or on-site services, with a focus on providing clear, concise,accurate, and fully compliant documentation, from early drug development through post-approval.

Synterexisseekingan organized, motivated, and collaborative individual for our medical writing team.Theseniormedical writer will partner cross-functionallywith client teams inClinical Development, Clinical Operations,Biostatistics,Regulatory, and Program Management inleading theplanning and preparation of high-quality clinical regulatory documents. The medical writer may produceprotocols, publications, study reports, investigator brochures,narratives,and module documents, according to clientand agency guidelines,to support drug development underbrisktimelines.

Location: Fully remote, but must be able to attend key (e.g., roundtable or kickoff) meetings on site with clients asrequested.

Essential Duties & Responsibilities
  • Lead theexecution of documents, includingproject management tasks such ascreating,maintaining, and communicatingtimelines
  • Coordinate cross-functional client contributors and stakeholders as well as internal resources (e.g., quality control [QC], publishing)to ensuretimelycompletion ofdocuments
  • Ensuredocument developmentadherestoanyrelevantclient processes, templates, and instructionaldocuments
  • Serve as an expert on client document management system and related tools, templates, and procedures to ensure efficient documentdevelopment
  • Lead document message development in collaboration withclient
  • Interpret data and create shell documents to supportauthoring
  • Plan and lead kickoffmeetings
  • Facilitate resolution of review feedback including planningand leadingcomment resolution meetings(curate review comments to ensuremeetings areefficient)
  • Follow-up with individual team members asneeded to resolve outstanding reviewfeedback
  • Ensure consistency among client programs in terms of messaging, formatting, and presentation ofdocuments
  • Conduct literature searches asneeded
  • Perform peer QC review asneeded
  • Contribute to medical writing operational initiatives (e.g., templates, style guides, reference management), if needed
Requirements
  • Experience (5+ years) as a medical writer in the CRO/biotech/pharmaceutical field
  • Bachelorโ€™s degreeor higherin a relevant field
  • Oncology, InfectiousDisease, or Vaccineexperiencedesired
  • Experiencedesiredin writingclinical study reports, protocols, protocol amendments, investigator brochures, module 2, and module 5documents
  • Flexibility towork across multiple therapeutic areas, if needed
  • Experiencewriting documents according toestablished processes and documenttemplates
  • Familiarity with lean authoring approachesand structured content management
  • Familiarity with the requirements for preparation of key clinical and regulatory documents, including ICH and US regulatory requirements; working knowledge of ex-US regulatory requirements isdesired
  • Expertisewith Microsoft Word and other Microsoft applications
  • Experiencedeveloping documentsusingdocument management systems, collaborative authoringtools, and reviewtools
  • Comfortableadaptingto newtools andtechnologies, if needed
  • Ability to work both independently and collaboratively in the face of competingpriorities
  • Service-oriented and proactive approach to projectmanagement
  • Excellent conflict management and negotiation skills
  • Comfortable providing suggestions based onpreviousexperience
  • Strong written and verbal communication skills

Synterexprovides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal,stateor local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence,compensationand training.

Synterexparticipates in the Department of Defenseโ€™sSkillBridgeprogram. For more information, please visit www.synterex.com/fellowships-internships.

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