FULL_TIME

FEED

OTHER

The Medical Writer provides support for all Investigator Initiated Trials (IIT) at the Perlmutter Cancer Center (PCC) across all campuses and report into the Protocol Development Monitoring Unit (PDMU) at the Clinical Trials Office (CTO) with a reporting line to the PCC Molecular Oncology program. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care.

NYU Langone Health

Medical Writer - Perlmutter Cancer Center Clinical Trials Office

silkroad ATS feed

UNKNOWN

HOUR

Other functions of the role include (but are not limited to) change planning, meeting facilitation and management, change proposal review, developing communications and leveraging employee feedback and data for improvement Partner with SMEs in the Supply Chain team in creating or revising various GMP documents, including (but not limited to) SOPs, forms, work instructions, specifications, Change Controls, etc.

Artech LLC

Technical Writer II

jobdiva

You will draw on your clinical expertise, leadership skills, and strategic insight to turn complex clinical data into clear, compelling educational projects, guiding them from concept to completion to meet educational needs of oncology audiences. Serve as a subject matter expert in support of business development initiatives, collaborating with sales teams to identify and present opportunities for funded projects and programs, and participate in project management activities as needed.

YEAR

MJH Life Sciences

Scientific Director

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As a global strategic partner that brings together strategy, evidence, engagement, and technology, we were designed to engineer breakthrough value to tackle our clients’ toughest challenges by revolutionizing how value is generated, demonstrated, and communicated. The Scientific Director/Associate Scientific Director will also direct the editorial component of projects, lead a team of medical writers, and ensure the accuracy, quality, and content of all written material.

Lumanity

Associate Scientific Director

[AW]-iCims

This position falls within our wider Medical Strategy and Communications division, which serves our clients by mobilizing our scientific knowledge to interpret data and create compelling narratives to guide their medical communications strategy in the context of the current therapeutic landscape and through regulatory challenges. As a global strategic partner that brings together strategy, evidence, engagement, and technology, we were designed to engineer breakthrough value to tackle our clients’ toughest challenges by revolutionizing how value is generated, demonstrated, and communicated.

Comprehend and apply relevant evidenced-based medical literature, clinical practice guidelines, and disease-state information for the development of content across various therapeutic areas (eg, identify levels of evidence, clinical trial data, clinical utility of therapeutic choices and unmet needs in treatment landscapes, product-specific education). As an Associate Scientific Director with Clinical Communications, you will be working closely with a Scientific Director (SD) and an internal team dedicated to producing content for live meeting and video projects that will educate and inform healthcare providers with the goal of improving outcomes of care.

sourcestack_via_bold

A minimum of 3 years of experience in a medical communications or agency setting required; 5+ years preferred for candidates expected to independently manage client relationships and lead junior staff from day one. Contribute to business development efforts as a scientific subject matter expert, working alongside client services to help identify program opportunities and inform proposals, scopes of work, and project planning.

Scientific Director (Oncology)

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.

ICON Plc

Senior Medical Writer

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Ecology employees may be eligible for the following: Medical/Dental/Vision for employee & dependent(s), Public Employees Retirement System (PERS), Vacation, Sick, and other Leave , 11 Paid Holidays per year , Public Service Loan Forgiveness, Tuition Waiver, Long Term Disability & Life Insurance, Deferred Compensation Programs, Dependent Care Assistance Program (DCAP), Flexible Spending Arrangement (FSA), Employee Assistance Program, Commute Trip Reduction Incentive, Combined Fund Drive, SmartHealth *Click here for more information. Required Qualifications: Nine years of combined education and/or experience performing related to the duties of the position, that includes the following: Experience collecting, researching, and analyzing complex hydrologic or hydrogeologic data to support technical evaluations and regulatory decisions.

State of Washington

Permit Writer (Environmental Specialist 4)

About the Department of Alumni Affairs and Development: The Office of Alumni Affairs and Development (AAD) at Harvard Medical School advances the School's mission by inspiring philanthropy, fostering lifelong engagement, and building enduring partnerships with alumni, donors, volunteers, and friends around the world. The Writer/Editor manages a portfolio of approximately 50 narrative stewardship reports annually, provides editorial support on an additional 50 reports, and contributes to other key writing projects and digital stewardship initiatives.

Harvard University

Writer/Editor, Donor Relations

Serve as the Medical Writing representative on assigned project teams and demonstrate document leadership: communicate content requirements, coordinate and conduct interdepartmental team review of draft and final documents, schedule and lead/facilitate authoring team meetings to agree on expectations, evaluate progress on tasks, identify issues and facilitate resolutions, manage/drive the timeline, and advance document development to approval, according to Parexel or client guidelines/SOPs. Gather, review, analyze, and evaluate pertinent resources to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and integrated summaries of safety and efficacy.

The expertise and passion for excellence shared by our people around the world unites us in our mission and drives our success. As a premier service provider to the global biopharmaceutical industry, we give you the opportunity to work with industry-leading clients in an exciting, collaborative environment where career choices and development paths are abundant, and projects are challenging. In fact, PAREXEL works with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. With over 30 years of experience, we have supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. We offer our employees the ability to make a difference globally, while we support them locally in environments full of challenge, collaboration, flexibility and industry-leading growth potential. Discover a career at PAREXEL, where exciting challenges and opportunities await you.

Parexel International Corp

Senior Medical Writer - FSP

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 Medicine Group LLC

Senior Medical Writer - Promotional Medical Writing

Essential Functions of the job: Works effectively with cross-functional groups to produce high-quality, scientifically accurate documents under strict timelines, and ensures consistency between related documents. Education Required: Senior Medical Writer -- at a minimum 4 years' relevant industry experience as a regulatory medical writer, plus a BA/BS degree; PhD/PharmD in life sciences preferre.

BeOne Medicines AG

Medical Writer, Market Access

Associate Medical Writer, Market Access

The Medical Writer is responsible for interpreting complex clinical study protocols and other medical/scientific documentation to prepare and coordinate laboratory specification and study‑specific medical/technical documents for ACM Global Laboratories. Maintain a general working knowledge of Food & Drug Administration (FDA), Medical & Healthcare Regulatory Agency (MHRA), New York State Department of Health (NYSDOH), Good Clinical Practice (GCP), ICH and other pertinent regulations.

Rochester Regional Health

Clinical Trials Medical Writer

Responsibilities include but are not limited to: Interacting with stakeholders including the federal government unit representatives, governance, and ECS service desk, operations, and engineering teams to understand the needs of end users and the enterprise. ECS is seeking a highly skilled and motivated Business Analyst/Tech Writer to help define and steer solutions and process improvements for our customers and teams.

ECS was founded in 2001 by experienced IT professionals with a commitment to quality processes, people and performance. Led by our Chairman, Roy Kapani, and an experienced executive leadership team, ECS provides our customers with solutions and services that support their critical needs and further mission objectives. This commitment has paved the way for expansive growth, year over year.
 
ECS gained market share in 2011 in the Department of Defense and Federal spaces through both organic and acquisition growth. In May, ECS completed its first strategic acquisition with the purchase of OAK Management, Inc., a leading provider of marine environmental services, ship systems engineering, maritime consulting and platform acquisition management. The OAK acquisition kicked off ECS’ intention to add tactical acquisitions as a part of its long term strategy to supplement and expand upon organic growth and to build enterprise value. ECS closed out 2011 with the acquisition of Paradigm Technologies, Inc. The Paradigm transaction added approximately 200 employees to ECS’ existing 900+ employees. Paradigm also added new Defense clients for ECS, including the Missile Defense Agency, the Navy’s Program Executive Officer for Integrated Warfare Systems, the United States Marine Corps, and the U.S. Marshals Service.
 
In 2012, ECS completed the acquisition of iLuMinA Solutions, Inc. iLuMinA brings large-scale Enterprise Resource Planning (ERP) software implementation and infrastructure design and development to ECS’ expanding capabilities.
 
ECS will continue to invest in corporate infrastructure and quality processes as we grow and enhance our ability to offer professional excellence to both our customers and our employees.

ECS Federal LLC

Business AnalystTechnical Writer

APL provides eligible staff with a comprehensive benefits package including retirement plans, paid time off, medical, dental, vision, life insurance, short-term disability, long-term disability, flexible spending accounts, education assistance, and training and development. You'll work closely with a hardworking team of engineers to compile highly technical information into easy-to-understand technical manuals, assessment reports, training materials and other Navy integrated logistics support products.

Johns Hopkins University Applied Physics Laboratory LLC

Technical Writer

At Jacobs, we're challenging today to reinvent tomorrow by solving the world's most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good. We are looking for someone who is comfortable working on large-scale, technically complex, multi-phase projects, specifying both interiors and exteriors, with exceptional communication skills and writing abilities, and a desire to be an effective collaborator and contributor to multiple project teams.

Jacobs Solutions Inc

Architectural Specifications Writer - Remote (LSNA-PA/OH/IN/NC)

The work will span regulated clinical AI and adjacent biomedical AI product development, including SaMD clinical support tools, autonomous patient-facing and clinical workflow agents with post-deployment oversight and safety monitoring, computer-vision image analysis systems, and AI-enabled medical devices (including edge AI and/or surgical robotics), with additional exposure to computational AI for drug discovery. Draft All Proposal Sections Draft all major proposal sections (not just outlines or edits), including technical narrative, significance/impact, innovation, work plan, milestones, evaluation/validation strategy, risk/mitigation, and related supporting sections as applicable.

Scientific Writer Jobs in the United States

Medical Writer - Perlmutter Cancer Center Clinical Trials Office NYU Langone Health

Technical Writer II Artech LLC

Scientific Director MJH Life Sciences

Associate Scientific Director Lumanity

Scientific Director Lumanity

Associate Scientific Director MJH Life Sciences

Scientific Director (Oncology) MJH Life Sciences

Senior Medical Writer ICON Plc

Permit Writer (Environmental Specialist 4) State of Washington

Writer/Editor, Donor Relations Harvard University

Senior Medical Writer - FSP Parexel International Corp

Senior Medical Writer - Promotional Medical Writing Precision Medicine Group LLC

Senior Medical Writer BeOne Medicines AG

Medical Writer, Market Access Precision Medicine Group LLC

Associate Medical Writer, Market Access Precision Medicine Group LLC

Clinical Trials Medical Writer Rochester Regional Health

Business AnalystTechnical Writer ECS Federal LLC

Technical Writer Johns Hopkins University Applied Physics Laboratory LLC

Architectural Specifications Writer - Remote (LSNA-PA/OH/IN/NC) Jacobs Solutions Inc

Lead Technical Writer, Clinical AI/ML & SaMD Grant Engine Jobs

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