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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.

HOUR

Nucleus Global Ltd

Lead Medical Writer

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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.

Senior Medical Writer

The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.

YEAR

SystImmune, Inc.

Medical Writer

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Position Summary: The medical writer will be responsible for the management and oversight of assigned medical writing projects, including clinical study protocols and reports, investigational new drug applications (INDs), investigator brochures, reviewing informed consent forms and regulatory briefing materials. Key Responsibilities: Write, edit and/or manage the production of high-quality clinical documentation including clinical study protocols, synopses, and clinical study reports for submission to regulatory authorities in support of marketing applications and BLAs.

Systimmune Inc

Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. American Medical Writers Association (AMWA) Board of Editors in the Life Science University of Chicago Medical Writing & Editing Program certification preferred.

Memorial Sloan-Kettering Cancer Center

Editor/Grant Writer, Department Of Surgery

Memorial Sloan Kettering Cancer Center

Editor/Grant Writer, Department of Surgery

FULL_TIME

Systimmune

partner JazzHR

Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Cross-Functional Collaboration, Healthcare Trends, Leverages Information, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Product Strategies, Scientific Communications, Strategic Thinking, Tactical Planning, Technical Credibility The anticipated base pay range for this position is: The Associate Medical Director acts, in collaboration with CAPLYTA Medical Affairs leadership, to connect therapeutic strategy with the clinical, scientific, and operational implementation of U.S.-focused company-sponsored or investigator-initiated studies supporting CAPLYTA.

6120-Janssen Scientific Affairs Legal Entity

Associate Medical Director

The senior medical writer will partner cross-functionally with client teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management in leading the planning and preparation of high-quality clinical regulatory documents. The medical writer may produce protocols, publications, study reports, investigator brochures, narratives, and module documents, according to client and agency guidelines, to support drug development under brisk timelines.

TransPerfect

Senior Medical Writer | US

The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Ability to successfully manage and prioritize writing projects with competing deadlines, to foster collaborative cross-functional relationships, and to drive high-quality regulatory writing projects to successful submission.

Revolution Medicines Inc

Principal Medical Writer

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.

The Associate Medical Writer at Pharmacy Times Continuing Education (PTCE) plays a vital role in supporting the Scientific Affairs and Business Development teams by contributing to the development of accredited continuing education (CE) content. This is an entry-level to early-career position, ideal for a strong writer with a working knowledge of life sciences, pharmacy, medicine, or a related field.

MJH Life Sciences

Associate Medical Writer

Health Interactions

Evaluate the following and take prompt and appropriate action where inadequacies are identified: datapackage, updates to medical literature, own work and effective and efficient management of projectresources (project box, scheduling, background information, databases, document tracking, and division of work within project team). Produce a range of written communications items in accordance with the needs of the client, target audience, target publication medium and level of design/creativity.

IPG MediaBrands

Mediabrands Worldwide Inc

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. 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.

Senior Medical Writer (Remote)

An advanced degree in a medical or science-related specialty (MD, PharmD, RN, NP, PA, PhD) is preferred; minimum of a Bachelor of Science degree (life sciences, public health, or clinical sciences) or similar with several years' relevant work experience required. Maintain up-to-date knowledge of key clinical issues within the therapeutic areas of interest; remain current with relevant literature; clinical practice guidelines; approved therapeutic drugs, regimens, and devices; and therapeutic pipelines.

WebMD Health Corp

Senior Medical Writer (Remote - US)

Comprehend and apply relevant evidence-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 a Medical Writer with the Clinical Communications team at MJH Life Sciences, you will play a vital role in developing educational publication content for healthcare professional audiences.

MJH Healthcare Holdings LLC

Medical Writer, Publications

The Center on Causal Data Science for Child and Adolescent Maltreatment Prevention (The CHAMP Center) seeks a data analyst to support its work determining predictive and causal models for child maltreatment exposures (e.g., physical abuse, sexual abuse, neglect) and outcomes (e.g., PTSD, depression, aggression). Perform statistical analysis of medical and research data using SPSS, Python, Excel, SQL, or other relevant tools; generate data listings, tables, figures, and reports from clinical or operational datasets.

Clinical Scientist Jobs in New Brunswick, NJ

Lead Medical Writer Nucleus Global Ltd

Senior Medical Writer Nucleus Global Ltd

Medical Writer SystImmune, Inc.

Medical Writer Systimmune Inc

Editor/Grant Writer, Department Of Surgery Memorial Sloan-Kettering Cancer Center

Editor/Grant Writer, Department of Surgery Memorial Sloan Kettering Cancer Center

Medical Writer Systimmune

Associate Medical Director 6120-Janssen Scientific Affairs Legal Entity

Senior Medical Writer | US TransPerfect

Principal Medical Writer Revolution Medicines Inc

Medical Writer Nucleus Global Ltd

Associate Medical Writer MJH Life Sciences

Senior Medical Writer Health Interactions

Medical Writer IPG MediaBrands

Medical Writer Mediabrands Worldwide Inc

Senior Medical Writer (Remote) MMS

Medical Writer WebMD Health Corp

Senior Medical Writer (Remote - US) MMS

Medical Writer, Publications MJH Healthcare Holdings LLC

Data Analyst New York University School of Medicine

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