UNKNOWN

FEED

At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. The role involves collaborating with internal and external clients, supporting and enabling effective and efficient communication that results in operational excellence.

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of nearly $11 billion, we have approximately 37,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries. We create value for our key stakeholders through two premier brands, Thermo Scientific and Fisher Scientific, which offer a unique combination of continuous technology development and the most convenient purchasing options. Our products and services help accelerate the pace of scientific discovery, and solve analytical challenges ranging from complex research to routine testing to field applications. All of our employees share a common set of values - Integrity, Intensity, Innovation and Involvement. Our ability to grow year after year is driven by our ability to attract, develop and retain world-class people who will thrive in our environment and share in our desire to improve mankind by enabling our customers to make the world healthier, cleaner and safer. If you share in our values and if you're looking for an employer who is strongly committed to developing talent and rewarding achievement, come grow with us at Thermo Fisher Scientific. Thermo Fisher Scientific is an Equal Employment Opportunity and Affirmative Action employer.

Thermo Fisher Scientific

Medical Writer - Medical Information

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Key responsibilities include: Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity. Collaborating closely with cross-functional teams, including clinical research, biostatistics, regulatory affairs, and medical affairs, to interpret and analyze clinical trial data, summarize scientific findings.

Senior Medical Writer

As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. The successful candidate will have a proven track record in authoring clinical regulatory documents; ideally they will also bring the versatility to author and support preclinical regulatory documents as part of a broader regulatory writing portfolio.

Thermo Fisher Scientific Inc

Senior Regulatory Medical Writer, Client-embedded, FSP

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With an emphasis on investigator-initiated, early phase clinical trials, the clinical research Protocol Writer works with clinical investigators to write, edit and complete clinical trial protocols and related documents necessary to accurately and timely submit clinical trial projects to the Scientific Review Committee (SRC). For select grants that include clinical trials, the position will work with Grant Administrators on the clinical research portion of the proposal, including developing the protocol and related documents outlined in the PHS Human Subjects and Clinical Trials Information Form as required for NIH defined clinical trials.

HOUR

H. Lee Moffitt Cancer Center & Research Institute Inc

PROTOCOL WRITER I

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.

YEAR

MJH Healthcare Holdings LLC

Medical Writer (Oncology)

H. Lee Moffitt Cancer Center and Research Institute

Protocol Writer I

Ataraxis has raised over $24 million in funding, including a $20 million Series A led by top venture capital funds such as Thiel Capital/Founders Fund (OpenAI, SpaceX, Palantir), Obvious Ventures (AMI Labs, Inceptive, Radical Numerics, Recursion), and AIX Ventures (Hugging Face, Perplexity). This is a rare opportunity that can grow into more scientific or more commercial roles long-term, and can provide significant upside, but will require people with more scientific background to handle commercial/sales-like conversations and focus on commercial outcomes.

Ataraxis AI

Scientific Engagement

The Scientific Affairs Manager is a key member of the content development team who utilizes their combined skills as a scientific medical writer, educational design innovator, and grant development specialist to conduct a turnkey process that includes educational grant development, followed by content development for awarded grants. Plan and develop well-written, scientifically accurate and current program content, including but not limited to presentation slide decks, interactive video program scripts, print monographs, and case studies, collaborating with internal clinical and editorial staff and external KOL experts.

Ziff Davis Inc

Scientific Affairs Manager - PRIME Education

PRIME Education, a property of Everyday Health Group, is looking for an Associate Director, who, with a high level of independence, will use their combined skills as a scientific medical writer, educational design innovator, and grant development specialist to conduct a turnkey process that includes educational grant development followed by content development for awarded grants. Contribute to grant planning and development, encompassing educational designs, formats, and execution plans, to meet department goals, generate robust outcomes, and address unmet educational and research needs to assist in strategic planning for future activities.

Associate Director, Scientific Affairs

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

Regardless of past practice, all resumes submitted by search firms to any employee of Nucleus Global and its affiliated companies via email, the Internet or in any form - without a current signed fee agreement for that position (as authorized by the Recruitment Manager) - will be deemed the sole property of Nucleus Global, and no fee will be paid in the event the candidate is hired as a result of the referral or through other means. You will be required to participate in client meetings / teleconferences and attend scientific meetings such as congress, symposia and advisory boards and participate in pre-meetings, onsite activities and post meeting work as required / appropriate.

Nucleus Global Ltd

Medical Writer

As part of Inizio Medical, our clients benefit from the synergies available within our global network of offices staffed by highly talented individuals who can deliver on a global scale or a local level and across a broad spectrum of therapy areas. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.

Lead Medical Writer

Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs. We consider compensation more than just a base salary - that's why we also offer an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work.

The Senior Manager, Scientific Communications & Publications plays a key role in the development and execution of scientific communication and publication activities supporting Serviers Neuromuscular Disease portfolio, including Duchenne Muscular Dystrophy (DMD), Becker Muscular Dystrophy (BMD), and emerging pipeline assets. Working closely with Medical Affairs, Clinical Development, HEOR, Global Publications, and external experts, this individual will support the planning, development, and execution of scientific publications and medical communication initiatives that facilitate the timely dissemination of clinical and scientific data to healthcare professionals and the broader scientific community.

Les Laboratoires Servier SAS

Senior Manager, Scientific Communications and Publication, Neurology

Experience Working in partnership with Client Services, you will help to establish a cohesive and dynamic relationship between the accounts and editorial teams and the client, leading discussions in client meetings/teleconferences (as required) to ensure client satisfaction is maintained at all levels. Drawn together from several backgrounds including the pharmaceutical industry, research, marketing, medical and regulatory writing, sales, publishing, digital media and design, we have the experience and all-round ability to conceive and deliver the best quality medical communications programs.

Scientific Director - Commercial

This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at myHR@precisionmedicinegrp.com.

Precision AQ

Associate Scientific Director, Medical Communications

FULL_TIME

You will serve as a key contributor to manuscript development, congress activities, publication project management, and scientific communications initiatives, partnering closely with Medical Affairs North America, Global Scientific Communications, Value & Evidence and other cross-functional partners, as well as external authors. As a Senior Medical Communications Writer on the Medical Affairs, North America team, you will be responsible for researching, writing, and editing scientific publications and communications materials that advance the understanding of rare MC4R pathway diseases and support Rhythm’s medical communications objectives.

Rhythm Pharmaceuticals

Senior Medical Communications Writer - Medical Affairs, North America

partner JazzHR

Operating across a network of CDMO sites, GMP analytical testing laboratories, and manufacturing support centers, we partner with clients to efficiently advance programs from early development through commercialization. Bachelor’s degree in a Life Sciences field, Quality Assurance, Technical Communication, or a related scientific discipline; AND three (3) or more years of experience in a pharmaceutical, medical device, cGMP, or other regulated environment.

Three divisions. Two countries. 1800 employees. Twenty-eight environmental labs. Two Life Sciences labs. Twenty-four service centers. Hundreds of certifications. 38 years of industry experience. Financial stability. Dynamic thought leadership and strategic management planning with one shared vision: work together to protect our environment and improve our health.
 
Pace began on a much smaller scale in 1978, serving Minneapolis and the surrounding areas with founder and CEO Steve Vanderboom at the helm. A commitment to safety and high ethical standards, respect for both clients and employees, and a drive for excellence inspired us as we expanded - and these values are at the core of everything we do today. Still under Vanderboom's directorship, we are proud to be industry leaders, offering an unparalleled range of services delivered by the most experienced scientific professionals. No matter the scope of work or special requirements, we have the people, knowledge and technology to tackle them. Partnering with us, clients are guaranteed to experience the Pace Analytical difference.
 
Pace Analytical Services, LLC. provides analytical services including environmental testing and sampling. Laboratories utilize EPA, ASTM Standard Methods, NIOSH and other accepted test procedures and methods in accordance with both federal and state regulations. Pace also provides specialty analytical support for air toxics, aquatic toxicity, bioassay, biota, dioxin/furans, low-level mercury, radiochemistry, vapor intrusion, environmental forensics, industrial hygiene, etc. 
 
Pace Analytical Life Sciences provides analytical testing services to the pharmaceutical/medical device industries. Services include chemical and microbiology, method development/validation, physical testing, raw material testing, stability testing and storage, and product release testing. Pace operates two FDA-registered, DEA-registered (Class I - V), cGMP-compliant facilities: one located in Oakdale, MN and the other located in San German, PR. The Oakdale, MN facility is ISO/IEC 17025:2005 accredited.
 
Pace Analytical Lab Ops Division provides professional scientific staffing - to accommodate full outsourcing or augmentation of staff at a client's on-site location - to various industries as well as research and development organizations. The ISO 9001:2008 certified Lab Ops Division also provides instrumentation sales, repair and qualification services, product and materials testing support and regulatory compliance services.

Pace Analytical Services

PLS Technical Writer

You will partner on a diverse portfolio of projects spanning multiple therapeutic areas (e.g., oncology, cardiology, neurology, etc.) and collaborate with interdisciplinary teams—including research scientists, medical professionals, medical science or scientific affairs liaisons, and commercial partners—to communicate research insights. Working knowledge in one of these areas: real-world data/evidence (RWD/RWE), human genomics, clinical research concepts, computational biology (machine learning, statistics, algorithms, bioinformatics), and/or oncology.

Tempus AI

Science Writer

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The QC Investigation Writer partners closely with QC analysts, laboratory management, Quality Assurance, Microbiology, Manufacturing, and other cross-functional teams to investigate atypical laboratory events, identify root causes, assess product impact, and develop effective corrective and preventive actions. Collect, review, and analyze laboratory data, test methods, chromatograms, worksheets, instrument records, environmental monitoring data, and supporting documentation to determine probable root cause and product impact.

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc). 
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

Scientific Writer Jobs in the United States

Medical Writer - Medical Information Thermo Fisher Scientific

Senior Medical Writer IRE

Senior Regulatory Medical Writer, Client-embedded, FSP Thermo Fisher Scientific Inc

PROTOCOL WRITER I H. Lee Moffitt Cancer Center & Research Institute Inc

Medical Writer (Oncology) MJH Healthcare Holdings LLC

Protocol Writer I H. Lee Moffitt Cancer Center and Research Institute

Scientific Engagement Ataraxis AI

Scientific Affairs Manager - PRIME Education Ziff Davis Inc

Associate Director, Scientific Affairs Ziff Davis Inc

Science Writer II The Scripps Research Institute

Medical Writer Nucleus Global Ltd

Lead Medical Writer Nucleus Global Ltd

Senior Medical Writer Nucleus Global Ltd

Senior Manager, Scientific Communications and Publication, Neurology Les Laboratoires Servier SAS

Scientific Director - Commercial Nucleus Global Ltd

Associate Scientific Director, Medical Communications Precision AQ

Senior Medical Communications Writer - Medical Affairs, North America Rhythm Pharmaceuticals

PLS Technical Writer Pace Analytical Services

Science Writer Tempus AI

Business Professional - Technical Writer Lancesoft

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