Writer and Author Jobs in New Jersey

Currently, there are no Writer and Author jobs available in New Jersey which match this search. You may wish to explore similar job titles on the Editorial jobs in New Jersey page or view related jobs below.
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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...
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...
Our Client – a global company with around 2,000 people in 14 locations worldwide is looking for a Technical Writerat their NJ headquarters location. Excellent Salary Job Posting # 1554 Job Title:Technical Writer Location: Mahwah, NJ Relocation: No - Prefer local only Compensation:Salary $55K-$65K Benefits: Full package including medical, dental, vision, etc. Job Description Create, manage an...
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...
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...
Alpha Consulting Corp Hopewell, NJ
Job Description JUNIOR LEVEL MEDICAL WRITER REQUIREMENT #14-01012 RECRUITER: MICHELLE ASHEN JOB LOCATION: HOPEWELL, NJ SEPTEMBER 19, 2014 Project Description: PhD / MD / PharmD in a relevant scientific discipline or MS / BS with a minimum of 3 years (MS) to 5 years (BS) in pharmaceutical regulatory documentation, or equivalent, and good understanding of requirements for regulatory submissio...
--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...
Bristol Myers Squibb Princeton, NJ
Description 1. Coordinate and author documents needed for regulatory submissions (e.g., Phase 1/2 CSRs, briefing documents, CTD summary documents, pharmacometrics reports, responses to Health Authorities), ensuring the coordination and integration of the scientific, medical, and regulatory input from development team members. 2. Participate in relevant document sub team(s) and ensure effective p...
Bristol Myers Squibb Princeton, NJ
Description 1. Coordinate and author regulatory documents (e.g. Phase 1/2 CSRs, immunogenicity reports, pharmacometrics reports, summary of ECG findings, etc), ensuring the coordination and integration of the scientific, medical, and regulatory input from development team members. 2. Participate in relevant filing subteam(s) and ensure effective planning and management of timelines for all compo...
Public Service Enterprise Group Hancocks Bridge, NJ
Responsible for creating, revising and reviewing Operations Department procedures for the Hope Creek Generating Station to ensure safe, efficient and cost effective operations. Developing procedures, including drafting, editing and revising, performing comment resolution for the Hope Creek Generating Station. Ensure technical accuracy and compliance with all nuclear standards, processes, and proce...
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...
Clinical Solutions Group Hopewell, NJ
•PhD/MD/PharmD in a relevant scientific discipline or MS / BS with a minimum of 3 years (MS) to 5 years (BS) in pharmaceutical regulatory documentation, or equivalent, and good understanding of requirements for regulatory submission documents. •Demonstrated strong writing skills as evidenced by good quality writing in pharmaceutical regulatory documentation and/or publications in peer-reviewe...
Responsible for creating, revising and reviewing Operations Department procedures for the Hope Creek Generating Station to ensure safe, efficient and cost effective operations. Developing procedures, including drafting, editing and revising, performing comment resolution for the Hope Creek Generating Station. Ensure technical accuracy and compliance with all nuclear standards, processes, and proce...
Express Scripts Franklin Lakes, NJ
Advance your career with the company that makes it easier for people to choose better health. Express Scripts is a leading healthcare company serving tens of millions of consumers. We are looking for individuals who are passionate, creative and committed to creating systems and service solutions that promote better health outcomes. Join the company that Fortune magazine ranked as one of the "Most...
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...
Summary: This position will support the Vice President of Corporate Strategy and assist the Federal Sales Group with identification and analysis of upcoming requirements marked within the corporate pipeline. You will lead the corporate proposal center and be responsible for content management, proposal volume management and production throughout the proposal lifecycle. Provide initial proposal po...
Novartis Pharmaceuticals East Hanover, NJ, 07936
This role will provide strategic and operational support, which includes coordinating and compiling quality control feedback to the clinical authors on Key Clinical Submission Documents included as part of New Drug Applications (NDA) and Marketing Authorization Application (MAA) global submissions. Major Accountabilities: 1. Primary contact for coordinating QC timing among Oncology Submission Ma...
NEW JERSEY Director of Scientific Affairs/Pharmacy CE Pharmacy Times Office of CPE As Scientific Director, your responsibilities will include content development of CE activities; work with freelancers, authors and faculty on development of scientific content; integration of comments and changes; timely and optimal execution of CE activities; and gather necessary medical and scientific informat...
Daiichi Sankyo Edison, NJ, 08817
Job Summary: Position is responsible for the preparation of protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), clinical sections of the CTD (2.5, 2.7.3, 2.7.4), integrated summaries of efficacy and safety (ISE and ISS), briefing books, and regulatory responses. The position will be responsible for hands-on writing as well as supervision of work performed by CRO/consultant writ...
Clerk, Publishing Industry - Grammar Geeks and Language Lovers Wanted - Administrative Assistant (Bergen County, NJ) Strong writing/proofing skills. Extremely VARIED tasks. Job Description: Entry-level admin position, with preference given to candidates who have strong writing and the drive to do varied tasks. Serious candidates must: -have meticulous grammar and writing skills; good proofrea...

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Editorial Career Tools

Writer

Salaries

$20,800.00 - $114,400.00
Typical Salary for Writer in New Jersey
(89 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Bachelor's
57.1%
Master's
19.4%
Some College Coursework Completed
14.3%
Associates
4.1%
Certification
2%
(98 Respondents)
Source: Monster.com Careerbenchmarking Tool

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