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Clinical Publishing Jobs (NOW HIRING)

Icon plc

Senior Non-Clinical Editor

Blue Bell, PA

Senior Clinical Editor ICON is a global healthcare intelligence and clinical research organisation ... Perform publishing of PDF documents to client submission-ready standards. May involve multiple ...

ICON

Senior Non-Clinical Editor

Blue Bell, PA · On-site +1

Senior Clinical Editor ICON is a global healthcare intelligence and clinical research organisation ... Perform publishing of PDF documents to client submission-ready standards. May involve multiple ...

System One

Clinical Lab Scientist I

Oro Valley, AZ · On-site

$30 - $32/hr

Analyze clinical trial data and publish findings * Ensure compliance with medical research regulations * Collaborate with healthcare professionals and research teams * Support drug and therapy ...

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Clinical Publishing information

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$22K

$125.3K

$206K

How much do clinical publishing jobs pay per year?

As of Jul 13, 2026, the average yearly pay for clinical publishing in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Clinical Publishing, and why are they important?

Excelling in Clinical Publishing requires a strong background in life sciences, medical writing, and regulatory guidelines, typically backed by a degree in a relevant field and experience with scientific documentation. Familiarity with document management systems, regulatory submission platforms (such as eCTD), and knowledge of ICH and GCP standards are commonly needed. Attention to detail, excellent organizational skills, and effective communication are vital soft skills for managing complex documentation and collaborating with cross-functional teams. These competencies ensure the accuracy, compliance, and timely delivery of clinical documents crucial for regulatory approval and successful clinical trials.

What are some common challenges faced in a Clinical Publishing role, and how can they be managed?

A common challenge in Clinical Publishing is coordinating document reviews and managing tight deadlines among cross-functional teams, such as medical writers, regulatory affairs, and clinical researchers. Navigating complex regulatory requirements and ensuring all documents meet compliance standards can also be demanding. Effective communication, strong project management skills, and familiarity with regulatory guidelines help professionals overcome these hurdles and deliver high-quality submissions on time.

What is the difference between Clinical Publishing vs Medical Writing?

AspectClinical PublishingMedical Writing
Required CredentialsTypically requires life sciences or healthcare-related degrees, with some roles needing advanced degrees or certificationsOften requires degrees in life sciences, healthcare, or related fields; certifications like AMWA are common
Work EnvironmentPublishing houses, pharmaceutical companies, or medical communication agenciesPharmaceutical companies, medical communication firms, or freelance
Industry UsageUsed in the context of preparing and publishing clinical trial data, regulatory documents, and scientific articlesFocused on creating clear, accurate scientific content for various audiences, including regulatory and educational materials

Clinical Publishing and Medical Writing share overlapping skills and credentials, but Clinical Publishing emphasizes the publication process of clinical data and scientific articles, often within publishing or regulatory contexts. Medical Writing is broader, covering the creation of scientific documents for regulatory submissions, educational materials, and more. Both roles require strong scientific knowledge and communication skills, but their primary focus and work environments differ slightly.

What is clinical publishing?

Clinical publishing refers to the process of preparing, reviewing, and disseminating clinical research documents, such as study protocols, clinical study reports, and regulatory submissions, to regulatory agencies, journals, and other stakeholders. Professionals in this field ensure that clinical trial data is accurately reported and complies with regulatory standards. They play a crucial role in bringing new medical treatments and products to market by ensuring transparency, accuracy, and ethical reporting of clinical research.
More about Clinical Publishing jobs
What cities are hiring for Clinical Publishing jobs? Cities with the most Clinical Publishing job openings:
What states have the most Clinical Publishing jobs? States with the most job openings for Clinical Publishing jobs include:
What job categories do people searching Clinical Publishing jobs look for? The top searched job categories for Clinical Publishing jobs are:
Clinical Publishing jobs near you
Clinical Manager

Clinical Manager

Integrated Resources INC

East Hanover, NJ

Contractor

Posted 14 days ago

Job description

Job Description

Responsible for all operational aspects of 1 or more OGD clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific aspects of clinical trial(s) as assigned. Responsible for program level activities as assigned.Ensure all operational trial deliverables are met according to timelines, budget, operational procedures and quality standards.

Provide input and contribute to the development of protocols and related documents, in the ongoing scientific review of clinical data, and in trial data analysis, reporting and publishing.

Prepare training materials and presentations related to the planning and conduct of the trial.

Prepare clinical outsourcing specifications. Responsible for management of Contract Research Organizations (CROs) and ensure adherence to scope of work within timelines and budget.

Manage interactions with Oncology Development Operations and other relevant functions including Drug Supply Management and client local medical organizations.

Accountable for accuracy of trial information in all trial databases and tracking systems.

Support the development, management and tracking of trial budget working closely with the appropriate partners in OGD..

Participate in the organization and logistics of various oversight and Advisory boards; attend meetings.

Point of contact for managing/answering questions related to trial procedures and patients' eligibility.

Write CTT meeting minutes. May occasionally deputize for the CTH at Clinical Trial Team meetings. May participate in International Clinical Team meetings.

Contribute to program level activities (e.g., tracking of OGD program-related publications, development of clinical sections of regulatory documents like Investigators' Brochures, briefing books, safety updates, IND/NDA submission documents, responses to Health Authorities questions).

Responsible for implementation of best practices and standards for trial management within the TA, including sharing lessons learned.

Contribute to talent and career development of OGD staff through active participation in on-boarding, training and mentoring activities. May serve as faculty member for OGD training programs.


Qualifications

Involvement in cross-functional, multicultural and international clinical trial teams; demonstrated capabilities in leading specific trial related activities like planning, executing, reporting and publishing activities.

Excellent communication, organization and tracking skills. Strong operational skills and demonstrated ability to meet timelines.

Proven networking skills and ability to train colleagues.

Proven ability to work both independently or in a team setting, including a matrix environment

Knowledge of Good Clinical Practice; thorough knowledge of clinical trial design; understanding of the overall drug development process.

Knowledge of principles for trial budgeting.

Basic knowledge of oncology and/or hematology preferable


Additional Information


Best Regards,

Anuj Mehta

9739673402

Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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