Medical Writer Jobs in New Jersey

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48 New Jersey Medical Writer jobs found on Monster.

Jobs 1 to 20 of 48
Qualifications: · Excellent writing skills. · Must have at least 4 years of medical writing experience within the pharmaceutical industry and at least 2 years of this experience must have been spent authoring clinical documents for regulatory submission. (Phase I development document authoring is a significant plus.) · An understanding of clinical pharmacology, clinical research methodology and...
Company: Yoh Medical Writer needed for a contract opportunity with Yoh's client located in Woodcliff Lake, NJ. What You'll Be Doing: - Work directly with clinical study teams, the Oncology medical writing teams, regulatory affairs personnel, and the publishing group in the preparation of scientifically valid regulatory documents. - Responsibilities include prepare regulatory documents on behal...
Company Confidential Parsippany, NJ, 07054
Our client, a leading pharmaceutical marketing agency focusing in professional advertising, is seeking an experienced Medical Writer to join its team.​ The agency is privately held, highly entrepreneurial, and has an excellent culture. The Medical Writer will be a key member of the Scientific Services group and will support one of the biggest accounts in the company. The Medical Writer will play a...
TechData is hiring for Associate Director of Biostatistics (Prefer Bayesian adaptive designs),SAS/Statistical Programmer(Some positions can be telecommuting), Biostatistician(Some can be telecommuting), Medical Writer, Regulatory Documentation Specialist, Senior Publishing Specialist, Sr. Clinical Supply Manager, Sr. Clinical Data Manager for our pharmaceutical clients in Northern NJ. We also have...
Celgene Corporation Basking Ridge, NJ
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
R&D - Global Regulatory Sciences & Pharmacovigilance (GRS&P) Hopewell, NJ
Description Author and coordinate safety-risk related documents including strategic safety-risk related documents needed for regulatory submissions, ensuring the coordination and integration of information from cross functional team authors. Participate in relevant subteams of the MST and ensure effective planning and management of timelines for all components of assigned documents. Collaborate w...
Quintiles Communications develops and produces a broad range of communications programs and materials on behalf of the pharmaceutical industry. Working with our pharmaceutical clients, our activities include publication planning, market access, organizing international symposia, developing educational programs for physicians and patients, producing clinical trial investigator and participant suppo...
Bristol Myers Squibb Hopewell, NJ
Description Author and coordinate safety-risk related documents including strategic safety-risk related documents needed for regulatory submissions, ensuring the coordination and integration of information from cross functional team authors. Participate in relevant subteams of the MST and ensure effective planning and management of timelines for all components of assigned documents. Collaborate w...
The Global Medical Writing department is responsible for ensuring that work undertaken meets the requirements of government regulatory agencies locally and worldwide. This responsibility includes the preparation of a variety of clinical documents including clinical study reports for Phase II to IV clinical trials run by Covance globally, in collaboration with other Covance units as necessary. It i...
Abbott Laboratories Inc Princeton, NJ
SR MEDICAL WRITER-140000094E Description Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approxi...
Novartis Pharmaceuticals Corporation East Hanover, NJ
151951BR Expert Medical Writer, Regulatory Medical Writing Pharma Global Develop NPH USA East Hanover, NJ USA Novartis Pharmaceuticals Corporation, East Hanover, NJ Research & Development Full Time Regular Apply knowledge of diverse therapeutic areas to write, edit and manage the production of high quality clinical documentation for submission to regulatory authorities in support of mark...
Novartis Pharmaceuticals Corporation East Hanover, NJ
151958BR Senior Medical Writer, RMW, IIS Pharma Global Develop NPH USA East Hanover, NJ USA Novartis Pharmaceuticals Corporation, East Hanover, NJ Research & Development Full Time Regular As Senior Medical Writer, Regulatory Medical Writing (RMW) for Integrated Information Sciences (IIS) prepare and write submission dossiers for new drug applications to the FDA, including risk management...
Abbott Laboratories Princeton, NJ, 08544
Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 69,000 people. Abbott is an Equal O...
The Global Medical Writing department is responsible for ensuring that work undertaken meets the requirements of government regulatory agencies locally and worldwide. This responsibility includes the preparation of a variety of clinical documents including clinical study reports for Phase II to IV clinical trials run by Covance globally, in collaboration with other Covance units as necessary. It i...
Novartis Pharmaceuticals East Hanover, NJ, 07936
As Senior Medical Writer, Regulatory Medical Writing (RMW) for Integrated Information Sciences (IIS) prepare and write submission dossiers for new drug applications to the FDA, including risk management plans (RMPs) and clinical overviews. Write and edit regulatory documents including clinical study reports (CSRs), development safety update reports (DSURs), RMPs, and contribute to Common Technical...
Job Description: Duties and Responsibilities % of Time Provide medical writing support for development programs by hands-on writing of protocols, IBs, and CSRs. Participate in appropriate development teams and internal strategy and operations meetings. 60% Manage/Assist documents through the review process (coordinating document review meetings, collate and reconcile comments from various funct...
Novartis Pharmaceuticals East Hanover, NJ, 07936
Apply knowledge of diverse therapeutic areas to write, edit and manage the production of high quality clinical documentation for submission to regulatory authorities in support of marketing applications. Act as a member of clinical trial teams and submission teams to write/edit ICH (International Conference on Harmonization) compliant Common Technical Documents including clinical study reports (CS...
Responsibilities may include but are not limited to: Preparation of clinical study reports or other regulatory documents supporting ongoing clinical development programs and their supportive appendices (or sections of these) by the incorporation of text, graphs, charts, tables, statistical analyses, etc. in a clear and accurate manner consistent with the target audience and regulatory requirement...
Job Description: Full-time Medical Writer Promotional Medical Communications company in North Jersey offering excellent benefits and competitive salary is seeking a full-time onsite Medical Writer. Must have an advanced scientific degree: (PhD, PharmD or MS in life sciences) and prior experience working in a promotional medical communications agency to be considered for this opportunity. Candidat...
PDS Tech, Inc. is seeking Medical Writer for our client in Woodcliff Lake, NJ. Work directly with clinical study teams, the Oncology medical writing teams, regulatory affairs personnel, and the publishing group in the preparation of scientifically valid regulatory documents. Responsibilities include prepare regulatory documents on behalf of in accordance with the ICH guidelines, international re...

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Healthcare Career Tools

Medical Writer

Salaries

$33,000.00 - $176,800.00
Typical Salary for Medical Writer in New Jersey
(41 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Master's
33.3%
Bachelor's
29.2%
Doctorate
20.8%
Professional
8.3%
High School
4.2%
Associates
4.2%
(24 Respondents)
Source: Monster.com Careerbenchmarking Tool

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