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Clinical Medical Writer Jobs (NOW HIRING)

Merican

Medical Writer

We are seeking a skilled Medical Writer to develop high-quality clinical and regulatory documents in compliance with industry standards and regulatory guidelines. * The ideal candidate will ...

Pulse Biosciences

OR · On-site

This role works closely with Clinical Affairs, Regulatory Affairs, R&D, and Quality Engineering to ... medical writing experience in the medical device or pharmaceutical industry or 7+ years general ...

Galderma S.A.

Medical Writer

Fort Worth, TX · On-site

Job Summary The Medical Writer, Medical Information is responsible for developing accurate ... Conducts literature searches and evaluates scientific and clinical data to support accurate ...

Envision Pharma Group

Medical Writer

$78.80K - $102.40K/yr

Advance your medical writing career with purpose and impact. Work shouldn't just be something we do ... An advanced degree in a life sciences or clinical discipline. * Demonstrable experience in a ...

Galderma

Medical Writer

Fort Worth, TX

Job Summary The Medical Writer, Medical Information is responsible for developing accurate ... Conducts literature searches and evaluates scientific and clinical data to support accurate ...

IQVIA

Principal Medical Writer

Durham, NC

Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practices (GCP), along with developments and advances in drug development/medical and/or ...

Medasource

Lead Medical Writer

Dublin, OH · On-site

$80 - $90/hr

As a Lead Medical Writer on a 2-month remote contract, you will autonomously author and review a range of clinical regulatory documents, including CTD Module II summaries, Clinical Overviews ...

Pulse Biosciences

Medical Writer

This role works closely with Clinical Affairs, Regulatory Affairs, R&D, and Quality Engineering to ... medical writing experience in the medical device or pharmaceutical industry or 7+ years general ...

BioTalent

Medical Writer

Philadelphia, PA · On-site

Medical Writer / Content Specialist - Healthcare Communications (Promotional) Hybrid - Philadelphia ... Our focus is helping translate complex clinical and scientific information into clear, practical ...

Integrated Resources INC

Medical Writer

Groton, CT · On-site

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Location: Groton, CT Duration: 3 years+ Our client is looking to hire the Medical Writer Company is looking for ...

IQVIA

Principal Medical Writer

Durham, NC

Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practices (GCP), along with developments and advances in drug development/medical and/or ...

Costello Medical

Analyst/Medical Writer

Boston, MA · On-site

Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...

Prometrika LLC

Senior Medical Writer

Cambridge, MA · On-site

$134.75K - $162.89K/yr

PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We're ...

Sobi

Principal Medical Writer

San Diego, CA · Hybrid

... Medical Writer, you will provide communication expertise and lead a strategy-driven approach to ... Assume primary responsibility for preparation of key clinical and regulatory documents and ...

IQVIA, Inc.

Principal Medical Writer

Durham, NC · On-site

Keeps abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practices (GCP), along with developments and advances in drug development/medical and/or ...

MMS

Senior Medical Writer (Remote)

Canton, MI · On-site

Write and edit clinical development documents, including but not limited to, clinical protocols ... Mentor medical writers and other members of the project team who are involved in the writing ...

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Clinical Medical Writer information

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$46

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How much do clinical medical writer jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical medical writer 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 are the key skills and qualifications needed to thrive as a Clinical Medical Writer, and why are they important?

To thrive as a Clinical Medical Writer, you need strong scientific knowledge, excellent writing skills, and typically a degree in life sciences or a related field. Familiarity with regulatory submission standards, referencing software (like EndNote), and guidelines such as ICH and CONSORT is essential. Attention to detail, critical thinking, and the ability to communicate complex data clearly are standout soft skills in this position. These abilities are crucial for producing accurate, compliant documents that effectively communicate clinical research findings to regulatory agencies and healthcare stakeholders.

How does a Clinical Medical Writer typically collaborate with clinical research teams during the development of regulatory documents?

Clinical Medical Writers work closely with cross-functional teams, including clinical researchers, statisticians, and project managers, to gather and interpret study data for regulatory documents such as clinical study reports and protocols. Effective collaboration involves frequent meetings to clarify data points, understand study outcomes, and ensure compliance with regulatory requirements. Good communication skills and the ability to synthesize complex scientific information are essential, as writers often serve as the bridge between technical experts and regulatory reviewers.

What does a Clinical Medical Writer do?

A Clinical Medical Writer is responsible for creating scientific documents related to clinical research, such as clinical study protocols, regulatory submission documents, and clinical study reports. They translate complex scientific data into clear, accurate, and compliant materials for regulatory agencies, healthcare professionals, and sometimes the public. Their work is essential in ensuring that the results of clinical trials are communicated effectively and meet all legal and regulatory requirements.

What is the difference between Clinical Medical Writer vs Medical Writer?

AspectClinical Medical WriterMedical Writer
Required credentialsTypically advanced degrees in life sciences or healthcare, certifications like AMWA or EMWASimilar credentials, often with broader backgrounds in science, journalism, or communications
Work environmentPharmaceutical, biotech, or healthcare companies; regulatory agenciesPublishing, marketing, healthcare communication agencies, or freelance
Employer & industry usagePrimarily in clinical research, drug development, and regulatory submissionWide-ranging, including scientific publications, marketing materials, and educational content
Search & comparison intentUnderstanding specific roles in clinical and regulatory contextsGeneral overview of medical writing professions

Clinical Medical Writers focus on creating documents for clinical trials and regulatory submissions within healthcare and pharma industries. Medical Writers have a broader scope, including scientific publications and marketing content. Both roles require strong scientific knowledge and writing skills, but Clinical Medical Writers specialize in clinical and regulatory documentation.

More about Clinical Medical Writer jobs
What cities are hiring for Clinical Medical Writer jobs? Cities with the most Clinical Medical Writer job openings:
What states have the most Clinical Medical Writer jobs? States with the most job openings for Clinical Medical Writer jobs include:
What job categories do people searching Clinical Medical Writer jobs look for? The top searched job categories for Clinical Medical Writer jobs are:
Clinical Medical Writer jobs near you
Infographic showing various Clinical Medical Writer job openings in the United States as of May 2026, with employment types broken down into 2% As Needed, 55% Full Time, 38% Part Time, 1% Temporary, and 4% Contract. Highlights an 100% Physical job distribution, with an average salary of $96,235 per year, or $46.3 per hour.
Medical Writer

Medical Writer

Merican

Remote

Other

This job post has expired today. Applications are no longer accepted.

Job description

Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.
Job Title: Medical Writer
Location: Paramus, NJ, 07652
Job Type: Temporary Assignment
Duration: 5 Months
Work Type: Remote
Shift: Mon-Fri 9.00 AM-5.00 PM
Job Description:
  • We are seeking a skilled Medical Writer to develop high-quality clinical and regulatory documents in compliance with industry standards and regulatory guidelines.
  • The ideal candidate will collaborate with cross-functional teams, including Clinical, Regulatory, Biostatistics, and Medical Affairs, to create well-structured, scientifically accurate, and regulatory-compliant documents.

DUTIES AND RESPONSIBILITIES
Regulatory Document Writing:
  • Prepare and author clinical and regulatory documents, including but not limited to:
  • Clinical Study Protocols (CSPs) and Protocol Amendments
  • Clinical Study Reports (CSRs)
  • Investigator's Brochures (IBs)
  • Informed Consent Forms (ICFs)
  • Common Technical Document (CTD) Modules (e.g., Module 2.5 Clinical Overview, Module 2.7 Clinical Summary)
  • Briefing Documents for Regulatory Authorities (e.g., FDA, EMA)
  • Periodic Safety Reports
  • Risk Management Plans (RMPs) and Pediatric Investigation Plans (PIPs)
  • New Drug Applications (NDAs), Biologics License Applications (BLAs), and Marketing Authorization Applications (MAAs)
  • Responses to regulatory queries

Clinical Development Support:
  • Develop and maintain clinical development plans, clinical trial protocols, and statistical analysis plans
  • Collaborate with clinical teams to ensure alignment of clinical documents with study objectives and regulatory requirements
  • Interpret complex scientific and clinical data and communicate findings clearly and concisely
  • Regulatory Compliance & Standards:
  • Ensure documents comply with ICH, GCP, FDA, EMA, and other applicable regulatory agency guidelines
  • Maintain up-to-date knowledge of regulatory writing best practices, industry trends, and evolving guideline

Collaboration & Review:
  • Work closely with cross-functional teams, including medical, clinical, regulatory, statistical, and quality assurance teams
  • Review and edit documents prepared by internal teams or external vendors to ensure scientific accuracy, clarity, and compliance
  • Participate in team meetings, regulatory interactions, and strategy discussions
  • Drive document production timelines according to established plans
  • Plan and manage multiple simultaneous document development projects with shifting priorities

EDUCATION PREFERRED :
  • Advanced degree (PhD, PharmD, MD, or MSc) in Life Sciences, Medicine, Pharmacy, or a related field

WORK EXPERIENCE:
  • Minimum 3-5 years of medical writing experience in the pharmaceutical, biotech, or CRO industry
  • Strong background in writing regulatory documents for clinical trials and submissions
  • Epilepsy or Neurology experience is a plus
  • Experience with drug development across different phases (Phase I-IV) is a plus
  • Strong understanding of the drug development process, clinical research concepts, clinical study conduct, clinical study data collection, regulatory requirements, and biostatistical concepts
  • Familiarity with medical terminology and ability to interpret complex clinical data
  • Strong understanding of the concepts of coding dictionaries (MedDRA, WHODrug, etc.)
  • Excellent scientific writing, editing, and document structuring skills
  • Ability to simplify complex scientific concepts for diverse audiences
  • Proficiency in ICH guidelines, GCP, and regulatory submission requirements (FDA, EMA, etc.)
  • Strong attention to detail, ability to manage multiple projects, and meet deadlines
  • Ability to work independently and collaboratively in a fast-paced environment
  • High level of Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
  • Experience with document management systems and publishing tools (e.g., EndNote, Adobe Acrobat, regulatory submission platforms)
  • Veeva experience

PHYSICAL AND MENTAL REQUIREMENTS
  • Ability to multitask
  • Maintain composure under pressure
  • Ability to follow verbal or written instructions and use of effective verbal communications
  • Adapts and adjusts to change and grasps information quickly
  • Detail-oriented

OTHER:
  • Must have excellent, concise, and clear written and oral communication skills; possess strong analytical and interpersonal skills, ability to work independently.
  • Highly motivated self-starter witha a positive attitude, possessing the initiative required to achieve desired goals both independently and within a team structure.
  • Demonstrated project management ability.
  • Excellent interpersonal, oral and written communication skills.
  • Strong relationship-building skills.
  • Team-oriented, with the ability to work effectively with others

TekWissen® Group is an equal opportunity employer supporting workforce diversity.
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About Merican

Sourced by ZipRecruiter

Merican is a IT Service consulting firm, specialized in Digital adoption and Business automation. With our diverse collection of skilled and committed consultants, technology companies, businesses and digital experts, we provide our subject expertise and our unique client service approach, a best-in-class global model of delivery suited to the business demands of our clients. We ensure that we implement future-oriented solutions for our clients via investments in people, solutions, technologies, competencies and infrastructure.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Columbia , MD, US

Year founded

2020

Social media

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