Medical Writer Jobs in New Jersey

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63 New Jersey Medical Writer jobs found on Monster.

Jobs 1 to 20 of 63
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 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...
Medhealth Recruiting Bridgewater, NJ
Description JOB SUMMARY The purpose of this job is to support the medical writing team with the creation of clinical documentation according to company guidelines and international governmental regulations and to present clinical data objectively in a clear, concise format. This is a position for an experienced medical writer who also has an interest and capacity to develop new and innovative pr...
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...
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...
Location: Bridgewater, NJ Job Category: Laboratory\Process\Device Development Jobs Requisition Number: 70069828-37450 Medical Writer Developer-70069828-37450 Description Job Summary: The purpose of this job is to support the medical writing team with the creation of clinical documentation according to company guidelines and international governmental regulations and to present clinical data ...
Medhealth Recruiting Bridgewater, NJ
Description JOB SUMMARY The purpose of this job is to create, without supervision, any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present clinical data objectively in a clear, concise format. This position is for an independent, proactive, experienced medical ...
Location: Bridgewater, NJ Job Category: Laboratory\Process\Device Development Jobs Requisition Number: 70069827-37449 Principal Medical Writer-70069827-37449 Description Job Summary: The purpose of this job is to create, without supervision, any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international...
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...
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...
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...
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...
Start a new search >> Save it Upload Resume See all jobs at this company Printer-Friendly Version Save this job Email this job Medical Writer The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, genetic information or any other characteristic protected by law. If yo...
Marten Transport Bridgewater, NJ
Company DescriptionNamed Crain's Largest Executive Recruiting Firm in New York City Green Key Resources is a premier executive recruitment firm specializing in permanent placement, contract consulting, temp-to-hire and temporary staffing within the following specialty areas: accounting-finance, healthcare nursing & allied health, pharmaceutical, financial service operations, alternative asset mana...
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...
--The primary responsibility of this role, as Senior Scientific Medical Writer, is: Act as the medical writing expert responsible for the research, writing and editing of study level and submission level documents. The incumbent will provide full lifecycle support from clinical study protocols through regulatory dossier preparation and submission. Responsibilities will include assuring quality and...

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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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