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Medical Writing Jobs in Edison, NJ (NOW HIRING)

Synterex

SeniorMedical Writer

Princeton, NJ · On-site +1

Synterex, Inc. is aglobalconsortium of highly experienced clinical development professionals specializing in medical writing, submission publishing, and clinical science and operations support.

MJH Life Sciences

Medical Writer

Cranbury, NJ · On-site

$85K - $100K/yr

The Medical Writer plays a critical role in creating accurate, engaging, and compliant scientific ... This is more than writing - it's about shaping content that informs, educates, and drives ...

MMS

Senior Medical Writer (Remote)

Jersey City, NJ · On-site

Complete writing assignments in a timely manner * Maintain timelines and workflow of writing ... Mentor medical writers and other members of the project team who are involved in the writing ...

MJH Life Sciences

Associate Medical Writer

Cranbury, NJ · On-site

$65K - $75K/yr

The Associate Medical Writer at Pharmacy Times Continuing Education™ (PTCE) plays a vital role in ... Strong research, writing, and communication skills with the ability to translate complex scientific ...

Integrated Resources INC

Medical Writer

Madison, NJ · On-site

An advanced degree preferred and at least 3 years medical writing experience and /or experience in pharmaceutical development. Strong functional literacy is desirable: for example a track record of ...

Costello Medical

Senior Medical Writer

New York, NY · On-site

$90K - $100K/yr

You will have the unique opportunity to continue to develop your scientific writing expertise ... About Costello Medical Costello Medical is a rapidly growing global healthcare agency specializing ...

Costello Medical

Senior Medical Writer

New York, NY · On-site

$90K - $100K/yr

You will take a leading role across a variety of medical communication projects, working alongside ... You will have the unique opportunity to continue to develop your scientific writing expertise ...

Costello Medical

Senior Medical Writer

New York, NY · Hybrid

$90K - $100K/yr

You will have the unique opportunity to continue to develop your scientific writing expertise ... About Costello Medical Costello Medical is a rapidly growing global healthcare agency specializing ...

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All JobsMedical Writing JobsMedical Writing Jobs in Edison, NJ

Medical Writing information

See Edison, NJ salary details

$11

$47

$81

How much do medical writing jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for medical writing in Edison, NJ is $47.90, according to ZipRecruiter salary data. Most workers in this role earn between $34.86 and $57.98 per hour, depending on experience, location, and employer.

What is medical writing?

Medical writing is the process of creating scientific documents by specialized writers in the healthcare, pharmaceutical, or biotechnology industries. These documents can include clinical trial reports, regulatory submissions, research manuscripts, patient education materials, and more. Medical writers must accurately present complex medical information in a clear, concise, and compliant manner, often working closely with researchers, doctors, and regulatory professionals. The role requires a strong understanding of medical terminology, scientific research, and regulatory guidelines.

What are medical writing jobs?

Medical writing jobs work in health care and science communities to compose documents and articles. Those who have medical writing jobs may draft many different kinds of papers, such as educational or promotional literature, medical abstracts for textbooks, or research documents. Other medical writing jobs include ghost-writing for prominent scientists or physicians, journalistic writing for scientific magazines, or creating content for marketing materials. Regardless of what field you are in, to obtain medical writing jobs, you must be able to decipher and interpret complicated information and write in a manner that your audience understands. For example, you may use medical jargon in scientific journals, but medical writers typically use simpler language when writing for the general public.

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

To thrive as a Medical Writer, you need strong scientific knowledge, excellent written communication skills, and typically a background in life sciences or healthcare. Familiarity with referencing software, regulatory guidelines, and document management systems is often required. Attention to detail, adaptability, and the ability to explain complex concepts clearly are valuable soft skills in this role. These abilities ensure the accurate and effective communication of medical information for regulatory, clinical, or educational purposes.

How does a medical writer typically collaborate with subject matter experts and regulatory teams during a project?

Medical writers regularly interact with subject matter experts (such as clinicians and researchers) to ensure scientific accuracy and clarity in documents like clinical study reports, publications, or regulatory submissions. They also work closely with regulatory teams to align content with current guidelines and submission requirements. This collaboration often involves attending meetings, managing document reviews, and incorporating diverse feedback to produce high-quality, compliant deliverables. Effective communication and project management skills are essential to coordinate these multi-disciplinary efforts and meet strict deadlines.

What is the difference between Medical Writing vs Medical Editing?

AspectMedical WritingMedical Editing
Required CredentialsTypically requires a background in life sciences, healthcare, or related fields; often a degree or certification in medical writingRequires strong knowledge of medical terminology and writing; often a background in healthcare, editing, or related fields
Work EnvironmentOften works independently or in teams, creating clinical documents, regulatory submissions, and educational materialsUsually works alongside writers, reviewing and refining medical documents for clarity, accuracy, and consistency
Employer & Industry UsageUsed in pharmaceutical, biotech, healthcare, and medical device industriesCommon in publishing, healthcare communications, and regulatory agencies

Medical Writing involves creating original medical content such as clinical study reports, regulatory documents, and educational materials. Medical Editing focuses on reviewing and refining these documents to ensure clarity, accuracy, and compliance. Both roles require strong medical knowledge, but Medical Writers produce content, while Medical Editors improve existing content.

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. Many medical writers also have opportunities for freelance work or consulting, which can impact income levels.

How do I become a medical writer?

To become a medical writer, typically a bachelor's degree in life sciences, healthcare, or a related field is required, often complemented by advanced degrees or certifications in medical writing or regulatory writing. Developing strong writing skills, understanding scientific and medical terminology, and gaining experience through internships or entry-level positions are important steps; familiarity with tools like Microsoft Word and reference management software can also be beneficial.

Is there a demand for medical writers?

Yes, there is a strong demand for medical writers due to the growth of the healthcare and pharmaceutical industries, regulatory requirements, and the need for clear scientific communication. Medical writers often work in pharmaceutical companies, medical communications agencies, or as freelancers, and proficiency in scientific terminology and regulatory guidelines enhances job prospects.

What does the medical writer do?

A medical writer creates clear, accurate, and scientifically supported documents such as research articles, regulatory submissions, clinical study reports, and patient education materials. They interpret complex medical data for diverse audiences and often work with subject matter experts, adhering to industry guidelines and using tools like reference management software. Strong writing skills and knowledge of medical terminology are essential for this role.
More about Medical Writing jobs

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For Medical Writing jobs in Edison, NJ, the most frequently searched job titles are:

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Medical Writing jobs near you
Infographic showing various Medical Writing job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 17% Part Time, 3% Temporary, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $99,628 per year, or $47.9 per hour.

SeniorMedical Writer

Synterex

Princeton, NJ • On-site, Remote

Full-time

Posted 12 days ago

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
  • Bachelor'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

For further information or to apply, please reach out tocareers@synterex.com.

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 Defense'sSkillBridgeprogram. For more information, please visit www.synterex.com/fellowships-internships.

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