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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EPS Corporation is currently seeking a Technical Publication Writer / Editor to join our Information Management Solutions group. Duties Include: Authoring and updating software manuals by collaborating with software developers and test engineers Proofreading/Quality Assurance (QA) of Content Development of content in using XML authoring tools and in S1000D or military specification compliant f...
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...
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...
--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...
UserEdge is pleased to be supporting our valued client on the following search for a VP of Technical Communications. This person will lead a diverse group (US, Canada, India) of technical writers, designers, and editors supporting financial services enterprise applications. The ideal candidate will have experience leading a global team and be well versed in best practices for documentation (incl...
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...
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...
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...
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...
Grammar and Eclectic Mix of Duties--Publishing Industry 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 proofreading skills are ...

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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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