UNKNOWN

ADAPTED_NOW

HOUR

Collaborate with department team members and with cross-functional team Subject Matter Experts (SMEs) to learn their internal processes to write, edit, and maintain process documentation. Resolve complex issues in creative and effective ways, using skills as an experienced technical communication professional with understanding of industry best practices and company objectives.

For over 20 years, TalentBurst Inc. has been an award-winning provider of cutting-edge Workforce Management Solutions. With a strong commitment to staying ahead in the tech landscape, we pioneer innovative approaches to talent acquisition. Our expertise spans Life Sciences, and Healthcare Staffing, Banking, Financial, IT, and Engineering, as well as Global Employer of Record (EOR), Agent of Record (AOR), State, Local Government and Education (SLED), and IC validation/compliance services. Additionally, our division, TalentProcure, leads the industry with offerings such as High Hazard Payroll, Managed Services, and Vendor on Premise (VOP) solutions.
Due to our prioritization of excellent standards, we are Joint Commission Certified and are a certified Minority Business Enterprise (MBE) in the USA and Canada. Supporting over 130 Fortune 500 companies globally, we excel in navigating the landscape of talent acquisition. In a world of constant change, we embrace developing people-centric solutions that address the unique demands of our clients. Stay connected by visiting our website and following us on social media!

TalentBurst, Inc.

Technical Writer 3 - Contract

Based on the clinical study protocol and statistical analysis plan, translate clinical results data tables, listings, and figures into a report of study outcomes, complete final checks for data consistency, and ensure compliance with applicable regulatory requirements. This role will be responsible for producing high-quality clinical and clinical regulatory documentation that requires a strong understanding of medical and regulatory concepts and terminology, as well as the ability to translate complex information into clear and concise documentation.

Medical Writer Contract - Contract

TEMPORARY

FULL_TIME

CONTRACTOR

POSTING_API

Responsibilities: Provide accurate, balanced, evidence-based, and timely responses to unsolicited medical and scientific inquiries from healthcare professionals, patients or caregivers, and internal colleagues, using approved response documents, current literature, and appropriate data on file. A key focus of the role will be supporting Medical Information readiness for the upcoming multiple myeloma launch, including development of scientific response resources, management of anticipated inquiry topics, and preparation of internal and external support teams.

Genesis10 is a professional technology services firm that operates under the brand names Genesis10, Dev10 and New Journey.  
 
<ul>
<li style="margin: 0; vertical-align: baseline; overflow-wrap: break-word; font-kerning: none">Genesis10 focuses on IT and business roles at Fortune 500 companies throughout the U.S. </li>
<li style="margin: 0; vertical-align: baseline">Dev10 provides entry-level professionals paid programming instruction to work on compelling projects at great companies as a Software Developer or Data Professional. </li>
<li style="margin: 0; vertical-align: baseline">New Journey focuses on placing individuals in non-IT roles.    </li>
</ul>
Our team of experienced recruiters can help you find the ideal job to help your build your career.  We care about people.  We care about you.

Genesis10

Associate Director*

FEED

Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. Join Pharmaron's Preclinical Research team as a Scientific Writer II / III, where you'll play a critical role in preparing high-quality nonclinical study protocols, reports, and scientific documentation supporting pharmaceutical and medical device research.

YEAR

Pharmaron

Scientific Writer II / III, Preclinical Research

Talent Acquisition

Experience with NIH or DOD research grant writing (R01 level, not post-doctoral fellowships), involvement with human observational or therapeutic studies, protocol design/writing for human sample, observational/retrospective or therapeutic studies. We are looking for a Scientific Writer / Project Development Scientist who will help lead clinical, translational, and basic research activities in partnership with Dr. Christine Lovly, Chief of the Thoracic Oncology Division at City of Hope.

City of Hope

Scientific Writer / Project Development Scientist

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Radial is seeking a Scientific Writer to shape and sharpen the scientific content our teams publish — editing research outputs for argument and clarity, drafting blog posts from interviews and raw results, and helping our scientists release work in formats better suited to it than a static PDF. Judgment about audience: you can tell the difference between documentation for a method's likely users, a post for a general scientific reader, and a proposal for a funder, and you write differently for each.

Astera Institute

Scientific Writer, Life Science (Radial)

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As a successful candidate, you will: Write, edit (content, style and grammar/spelling), and proofread¬ R01 and R01-like grant proposals, scientific manuscripts for peer review, INDs, clinical and IRB protocols, or other scientific documents for faculty, research fellows, and students. Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we''re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.

Scientific Writer - Orange County

Writer must have a basic understanding of modern biology and chemistry and advanced knowledge (e.g., a graduate degree) in one or more of the following subject areas: biochemistry, molecular biology, cellular biology, biophysics, genetics, immunology, neuroscience, organic chemistry, chemical kinetics, pharmacology, animal physiology, medicine, public health. Calibr-Skaggs' drug development portfolio spans a broad range of human diseases, including cancer, autoimmunity and inflammatory diseases, metabolic and cardiovascular diseases, infectious and neglected tropical diseases, as well as age-related and degenerative diseases.

The Scripps Research Institute

Science Writer II

This role will be responsible for producing high-quality clinical and clinical regulatory documentation that requires a strong understanding of medical and regulatory concepts and terminology, as well as the ability to translate complex information into clear and concise documentation. Based on the clinical study protocol and statistical analysis plan, translate clinical results data tables, listings, and figures into a report of study outcomes, complete final checks for data consistency, and ensure compliance with applicable regulatory requirements.

Medical Writer 2

jobdiva

Collaborate with department team members and with cross-functional team Subject Matter Experts (SMEs) to learn their internal processes to write, edit, and maintain process documentation. " Resolve complex issues in creative and effective ways, using skills as an experienced technical communication professional with understanding of industry best practices and company objectives.

Technical Writer 3

Looking for a great job? Join eTeam. We’re looking for talented staffing professionals to join our staff. We also provide contract assignments and full-time jobs at Fortune 2000 Companies. We’ve been named one of the best companies to work for by Staffing Industry Analysts and New Jersey Business.

eTeam Inc.

This role conducts systematic literature searches, appraises scientific evidence, and collaborates cross-functionally across Scientific Affairs, Clinical Research, Regulatory Affairs, Engineering, and Marketing to support product portfolio compliance and clinical communications. · Prepare literature review reports, evidence summaries, state-of-the-art analyses, clinical data appraisals, and benefit-risk assessments, · Monitor emerging scientific literature and technological developments relevant to Masimo products, therapeutic areas, and competitive technologies.

Danaher is a global science & technology innovator committed to helping our customers solve complex challenges and improve quality of life worldwide. Our world class brands are leaders in some of the most demanding and attractive industries, including life sciences, medical diagnostics, dental, environmental and applied solutions. Our globally diverse team of 71,000 associates is united by a common culture and operating system, the Danaher Business System, which serves as our competitive advantage. We generated $19.9B in revenue last year. We are ranked #162 on the Fortune 500 and our stock has outperformed the S&P 500 by more than 5,200% over 25 years.
At Danaher, you can build a career in a way no other company can duplicate. Our brands allow us to offer dynamic careers across multiple industries. We're innovative, fast-paced, results-oriented, and we win. We need talented people to keep winning. Here you'll learn how DBS is used to shape strategy, focus execution, align our people, and create value for customers and shareholders. Come join our winning team.
Danaher is committed to competitive compensation that typically has key components including base salary, variable annual incentive compensation based on personal and company performance, and long-term incentive.

Danaher

Senior Medical Writer

Reporting directly to the Chief Medical Officer, this individual will lead the writing of clinical study reports, regulatory submissions, and scientific communications in support of the company's Phase II and Phase III clinical trial programs. The Role: The Medical Writer will serve as an important contributor to Sagimet Biosciences' Clinical and Regulatory Affairs teams, responsible for the creation, coordination, and delivery of high-quality clinical and regulatory documents.

Sagimet Biosciences Inc

The purpose of this job is to support clinical evaluation reports (CERs) per Medical Device Regulation (MDR), to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, recertification and proposed indication/labeling changes, as well as CER updates to maintain EU product conformance. Competency Requirements: (Competency is based on: education, training, skills and experience.)In order to adequately perform the responsibilities of this position the individual must: " Previous experience in the application of therapeutic and device knowledge to support the development of clinical evaluation reports.

However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. This position partners closely with Regulatory Affairs, Research and Development, Clinical, Marketing, and Quality teams to ensure clinical evidence is effectively evaluated, communicated, and applied throughout the product lifecycle.

Stryker

Senior Staff Medical Writer (Remote)

Collaborate with department team members and with cross-functional team Subject Matter Experts (SMEs) to learn their internal processes to write, edit, and maintain process documentation. • Resolve complex issues in creative and effective ways, using skills as an experienced technical communication professional with understanding of industry best practices and company objectives.

Integrated Resources, Inc

Prior experience using AI for medical writing is not required, but candidates should be able to learn quickly how to use these tools in drafting, summarizing, comparing documents and quality control, while checking all AI-generated content against source documents to maintain accuracy, traceability and compliance. You will collaborate with cross-functional teams, including clinical researchers, regulatory professionals, and subject matter experts, to produce materials that support the advancement of clinical trials, product development, and regulatory submissions.

Rezolute

Medical Writer II, Clinical/Regulatory

Develop accurate, high-quality written content for digital, video, and event deliverables; ensure all content and supporting artwork are factually accurate, properly annotated, and referenced in accordance with in-house style guidelines and the AMA Manual of Style (11th edition). Working closely with an internal team of writers, editors, and project managers, you will independently develop peer-reviewed manuscripts, slide decks, video-based learning, and other content across the oncology landscape.

MJH Healthcare Holdings LLC

Medical Writer (Oncology)

Filling this need with a regular full-time employee will enable BioMarin to reduce writing-related CRO and contractor costs, increase Clinical Medical Writing productivity to meet development needs, and realize efficiencies and consistent documentation quality across programs through repeatable processes and continuity of knowledge of programs, investigational products, and indications. Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets.

BioMarin Pharmaceutical Inc

Principal Clinical Medical Writer

The Associate Director, Scientific Communications will play a key role within the Medical and Patient Affairs team, supporting the development and delivery of high-quality scientific and patient-friendly content that communicates the value and impact of Encoded’s programs. Support alignment with Research, Clinical Development, Corporate Communications, Regulatory Affairs, Patient Advocacy, and Commercial teams to ensure consistency of medical messaging across programs and audiences.

Scientific Writer Jobs in California

Technical Writer 3 - Contract TalentBurst, Inc.

Medical Writer Contract - Contract TalentBurst, Inc.

Associate Director* Genesis10

Scientific Writer II / III, Preclinical Research Pharmaron

Scientific Writer / Project Development Scientist City of Hope

Scientific Writer, Life Science (Radial) Astera Institute

Scientific Writer - Orange County City of Hope

Science Writer II The Scripps Research Institute

Medical Writer 2 TalentBurst, Inc.

Technical Writer 3 TalentBurst, Inc.

Technical Writer 3 eTeam Inc.

Senior Medical Writer Danaher

Senior Medical Writer Sagimet Biosciences Inc

Medical Writer 2 eTeam Inc.

Senior Staff Medical Writer (Remote) Stryker

Technical Writer 3 Integrated Resources, Inc

Medical Writer II, Clinical/Regulatory Rezolute

Medical Writer (Oncology) MJH Healthcare Holdings LLC

Principal Clinical Medical Writer BioMarin Pharmaceutical Inc

Associate Director, Scientific Communications Encoded Therapeutics

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