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Medical Writer Informed Consent Forms Jobs (NOW HIRING)

MMS

Senior Medical Writer (Remote)

Phoenix, AZ · On-site

... consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 ... Mentor medical writers and other members of the project team who are involved in the writing ...

BioFire Diagnostics

Medical Writer

Salt Lake City, UT

$95K - $124K/yr

By ensuring that evidence is robust, relevant, and strategically presented, the Medical Writer supports informed decision making and upholds the scientific credibility of the organization. The ...

bioMérieux

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

By ensuring that evidence is robust, relevant, and strategically presented, the Medical Writer supports informed decision making and upholds the scientific credibility of the organization. The ...

bioMerieux

Medical Writer

Salt Lake City, UT

$95K - $124K/yr

By ensuring that evidence is robust, relevant, and strategically presented, the Medical Writer supports informed decision making and upholds the scientific credibility of the organization. The ...

bioMerieux Inc.

Medical Writer

Salt Lake City, UT

$95K - $124K/yr

By ensuring that evidence is robust, relevant, and strategically presented, the Medical Writer supports informed decision making and upholds the scientific credibility of the organization. The ...

Biomerieux

Medical Writer

Salt Lake City, UT · On-site

$95K - $124K/yr

By ensuring that evidence is robust, relevant, and strategically presented, the Medical Writer supports informed decision making and upholds the scientific credibility of the organization. The ...

Integrated Resources INC

Medical Writer

Cambridge, MA · On-site

Serves as lead Medical Writer for key programs. Coordinates medical writing support for programs ... Informed Consents, Model Privacy Consents, Investigator Brochures, Clinical Study Reports, and ...

Castle Biosciences

Medical Writer

Friendswood, TX · On-site

Company Stock Grant Upon Hire A DAY IN THE LIFE OF a R&D Medical Writer As a Medical Writer, you ... We believe that disease management and treatment decisions can be better informed through a person ...

Real Chemistry

Medical Writer

$75K - $85K/yr

Our drive to transform healthcare is informed by our blend of deep scientific expertise, human ... Real Chemistry is looking for a Medical Writer to join our growing team! This is a hybrid role ...

Bioclinica

Associate Medical Writer

Princeton, NJ · On-site

The Medical Writer is also expected to provide guidance and support to the Clinical Project ... Creating, modifying and finalizing Site Manuals, associated fillable forms, Quick Reference Guides ...

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Medical Writer Informed Consent Forms information

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How much do medical writer informed consent forms jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for medical writer informed consent forms 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 some common challenges faced by Medical Writers specializing in Informed Consent Forms, and how can they be addressed?

Medical Writers focusing on Informed Consent Forms (ICFs) often encounter the challenge of translating complex medical and regulatory information into clear, patient-friendly language while ensuring compliance with ethical and legal standards. Balancing scientific accuracy with readability for a lay audience can be demanding, especially when dealing with intricate clinical trial protocols. Collaborating closely with clinical teams, ethics committees, and regulatory experts is key to ensuring all stakeholder requirements are met. Staying updated on evolving regulatory guidelines and participating in peer reviews can also help maintain high-quality, compliant documents.

What is the difference between Medical Writer Informed Consent Forms vs Medical Writer Clinical Study Protocols?

AspectMedical Writer Informed Consent FormsMedical Writer Clinical Study Protocols
PurposeTo explain study details to participants and obtain consentTo outline study design, procedures, and methodology for regulatory approval
Content FocusParticipant rights, risks, benefits, and confidentialityStudy objectives, methodology, endpoints, and regulatory compliance
Work EnvironmentCollaborates with clinical teams, IRBs, and regulatory bodiesWorks with clinical researchers, regulatory agencies, and sponsors
Required SkillsClear communication, understanding of ethics, regulatory knowledgeScientific writing, regulatory guidelines, detailed technical knowledge

Medical Writer Informed Consent Forms focus on creating documents that inform participants about the study, while Medical Writer Clinical Study Protocols develop comprehensive plans for conducting the study. Both roles require strong scientific writing skills and regulatory understanding but serve different purposes within clinical research.

What are Medical Writer Informed Consent Forms?

Medical Writer Informed Consent Forms are documents created by specialized medical writers to ensure that participants in clinical trials are fully informed about the study, its risks, benefits, and their rights before agreeing to participate. These writers use their expertise to translate complex medical and legal information into clear, understandable language for potential participants. Their work is crucial to ensure ethical standards and regulatory compliance in clinical research. Informed consent forms must be accurate, comprehensive, and tailored to the target audience’s level of understanding.

What are the key skills and qualifications needed to thrive as a Medical Writer specializing in Informed Consent Forms, and why are they important?

To thrive as a Medical Writer specializing in Informed Consent Forms, you need expertise in medical terminology, clinical research processes, and regulatory requirements, often supported by a degree in life sciences or a related field. Familiarity with document management systems, regulatory databases (such as IRB portals), and guidelines like ICH-GCP is crucial. Exceptional attention to detail, clear communication, and the ability to translate complex medical information into lay language are key soft skills. These competencies ensure the creation of accurate, compliant, and easily understood consent documents that protect patient rights and facilitate ethical clinical research.
Infographic showing various Medical Writer Informed Consent Forms job openings in the United States as of June 2026, with employment types broken down into 78% Full Time, 11% Part Time, and 11% Contract. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $96,235 per year, or $46.3 per hour.

Senior Medical Writer (Remote)

MMS

Phoenix, AZ • On-site

Full-time

Posted 14 hours ago

Job description

About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
  • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
  • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
  • Complete writing assignments in a timely manner
  • Maintain timelines and workflow of writing assignments
  • Practice good internal and external customer service
  • Highly proficient with styles of writing for various regulatory documents
  • Expert proficiency with client templates & style guides
  • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
  • Contribute substantially to, or manages, production of interpretive guides
  • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
  • Mentor medical writers and other members of the project team who are involved in the writing process
Requirements
  • At least 3 years of previous experience in the pharmaceutical industry
  • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
  • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
  • Understanding of clinical data
  • Exceptional writing skills are a must
  • Excellent organizational skills and the ability to multi-task are essential prerequisites
  • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
  • Experience being a project lead, or managing a project team
  • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
  • Not required, but experience with orphan drug designations and PSP/PIPs a plus

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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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