Blog writer Jobs in Raleigh, NC
Create a job alert for this search
Blog writer • raleigh nc
Last updated: 22 hours ago
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical resea...Show moreLast updated: 30+ days ago
Millions of people across the country are navigating mental health conditions, substance use disorders, and eating disorders, but too often, they're met with barriers to care.From limited local...Show moreLast updated: 30+ days ago
At Nutrient, we equip developers and innovators with cutting-edge tools to simplify workflows and accelerate impactful software creation.
We’re on a mission to redefine how documents are created, sh...Show moreLast updated: 30+ days ago
We want to be recognized as an international group focused on research, able to develop and commercialize innovative therapeutic solutions to improve the quality of people's lives.We intend to main...Show moreLast updated: 30+ days ago
We are committed to excellence and recognize the dedication it takes to do a great job.Join Our Team as a Mechanical Service Writer!.
Snider Fleet Solutions is seeking a Mechanical Service Writer wh...Show moreLast updated: 30+ days ago
Raleigh, NC The IT Trainer / Technical Writer is tasked with documentation of training materials in support of the DIT transition to ServiceNow and the procedural documentation of Standard Pre-Appro...Show moreLast updated: 30+ days ago
Primary Location : Raleigh, North Carolina.V-Soft Consulting is currently hiring for a.Prior experience developing APDs or related documents (e.
Working knowledge of government regulations as they pe...Show moreLast updated: 30+ days ago
Now Hiring : A Certified Rock Star (Service Advisor).Autohaus Import Service – Raleigh, NC.Are You the Headliner We've Been Waiting For? ??.
Hey there, I’m Doug Rogers.My wife and I o...Show moreLast updated: 11 days ago
Remote - must reside in one of the following states : CO, CT, DE, FL, GA, IL, MA, MD, MO, NC, NE, NJ, NY, NV, PA, SC, TN, TX, VA, or WV.
Must be eligible to work in the U.No C2C or 3rd-party submissi...Show moreLast updated: 30+ days ago
Join a global community of talented professionals to shape the future of AI.Earn up to $15 USD / hr and additional rewards based on quality of submission.
Outlier is committed to improving the intelli...Show moreLast updated: 22 hours ago
A company is looking for a Medical Writer.Key Responsibilities Produce quality scientific / medical writing across multiple business units and projects Develop coherent and logical content based o...Show moreLast updated: 30+ days ago
Parexel FSP is looking for a Principal Medical Writer! This is a remote role anywhere in the United States or Canada.The Medical Writer, Medical Writing, is responsible for writing and overseeing t...Show moreLast updated: 13 days ago
Earn up to $16 USD / hourly and work remotely and flexibly.Outlier, a platform owned and operated by Scale AI, is looking for.
If you're passionate about improving models and excited by the future of ...Show moreLast updated: 12 days ago
Tech can help you avoid the daunting task of writing and posting job offers, shifting through resumes and laboring through the lengthy interview process.
Our Staffing solutions will allow you to elu...Show moreLast updated: 2 days ago
Specifications Writer – Design Workshop Base pay range : $85,000 – $100,000 per year.Overview We seek licensed Landscape Architects with specifications expertise.
We believe that when environment, ec...Show moreLast updated: 19 days ago
Our mission : to eliminate every barrier to mental health.At Spring Health, we're on a mission to revolutionize mental healthcare by removing every barrier that prevents people from getting the help...Show moreLast updated: 24 days ago
Help make the American dream come true for immigrants! This is an exciting opportunity to grow your career with one of the largest law firms in the United States.
Ogletree Deakins is an internationa...Show moreLast updated: 6 days ago
Sr Medical Writer - Narrative Writer.Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical ...Show moreLast updated: 4 days ago
The Advanced Planning Writer develops Advanced Planning Documents, Medicaid Detail Budget Tables and other documentation required for the planning, implementation, and operations activities in supp...Show moreLast updated: 7 days ago
- Promoted
Nonclinical Writer
MMSRaleigh, NC, USFull-time
- Promoted
Curriculum Writer
Charlie HealthRaleigh, NC, USFull-time
Technical Writer
NutrientRaleigh, North Carolina, United States, 27601Full-time
Medical Safety Writer
CHIESI USACary, NCFull-time
- Promoted
Mechanical Service Writer
Snider Fleet SolutionsRaleigh, NC, USFull-time
Technical Writer
omega solutions incraleigh, North Carolina, United StatesFull-time
DHB / NC HIEA APD Writer
V-Soft ConsultingRaleigh, NC, United StatesFull-time
- Promoted
Automotive Service Writer / Advisor
NC AutohausRaleigh, NC, USFull-time
Technical Writer
AlphanumericRaleigh, NC, USFull-time
- Promoted
- New!
Blog Writing Intern (Remote)
Scale AIWest Raleigh, North Carolina, United StatesRemote
Full-time
Medical Writer
VirtualVocationsRaleigh, North Carolina, United StatesFull-time
Principal Medical Writer- FSP
PAREXELRaleigh, NC, United StatesFull-time
- Promoted
Freelance Writer
OutlierCary, NC, United StatesRemote
Full-time
Technical Writer
vTech Solution, Inc.Raleigh, NC, United StatesFull-time
Specifications Writer
Design WorkshopRaleigh, NC, United StatesFull-time
- Promoted
RFP Manager & Proposal Writer
Spring HealthRaleigh, NC, USFull-time
Immigration Legal Writer
Ogletree DeakinsRaleigh, NC, United StatesPermanent
Sr Medical Writer - Narrative Writer
Syneos Health / inVentiv Health Commercial LLCRaleigh, NC, United StatesFull-time
Advanced Planning Document Writer
STIRaleigh, NC, United StatesFull-time
- retail management (from $ 45,044 to $ 412,500 year)
- dentist (from $ 50,000 to $ 250,000 year)
- general dentist (from $ 180,000 to $ 250,000 year)
- product director (from $ 140,000 to $ 242,500 year)
- medical director (from $ 146,743 to $ 240,000 year)
- event planning (from $ 42,900 to $ 233,025 year)
- physician (from $ 84,928 to $ 227,750 year)
- associate dentist (from $ 162,500 to $ 224,500 year)
- software engineering manager (from $ 137,100 to $ 222,200 year)
- owner operator (from $ 88,650 to $ 221,000 year)
The average salary range is between $ 33,638 and $ 102,781 year , with the average salary hovering around $ 43,875 year .
Nonclinical Writer
MMSRaleigh, NC, US30+ days ago
Job type
- Full-time
Job descriptionBS + in pharmacology, toxicology, biology or chemistry, or related field, with industry experience within regulatory writing, regulatory affairs, laboratory sciences, quality assurance / control Knowledge of GLP, ICH guidelines, and applicable regulatory requirements 2+ years of pharmaceutical regulatory nonclinical writing experience Strong writing and analytical skills Proficiency with MS Office applications. Hands-on experience with clinical trial and pharmaceutical development preferred Basic understanding of CROs and scientific & nonclinical data / terminology, & the drug development process
Job Description
Job Description
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This person will participate in the development, writing, and management of highly technical nonclinical documents. This is a full-time, remote position.
Roles and Responsibilities :
- Strong experience with development and writing of nonclinical documents (eg, Module 2.4 and 2.6 eCTD submission documents, Investigator’s Brochure [IB], Nonclinical Study Reports, Meeting Requests, Briefing Documents, RTQs)
- Lead projects independently with minimal oversight, lead the writing (structure, content and messaging) of nonclinical documents, ensure the nonclinical package aligns with current regulatory guidelines and meets scientific integrity
- Ability to author based on highly technical sources such as GLP and non-GLP nonclinical study reports, in vivo and in vitro nonclinical data
- Ability to develop a mapping plan for the placement of nonclinical studies within structure of Module 2.4 and 2.6 eCTD submission documents
- Interpret and analyze applicable pharmacokinetics, pharmacology, and toxicology data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK / TK evaluation reports)
- Collaborate with cross-functional teams such as project management, safety, efficacy, biostats, regulatory operations, and CMC
- Demonstrated ability to lead others to complete complex projects
- Ability to complete documents according to sponsor’s format, processes, and according to regulatory guidelines
- Ability to effectively operate in an environment that requires negotiation, persuasion, collaboration, and analytical judgment
- Organizational expert within the nonclinical subject area
- Excellent written / oral communication and strong time and project management skills
- Ability to attend regular team meetings, lead client meeting and CRMs
- Ability to work in various client systems (eg, SharePoint, Veeva RIM, PleaseReview, EndNote), templates and toolbars
- Strong understanding of regulatory guidances as it applies to nonclinical submission documents and drug development (eg, ICH, FDA and EMA regulations and guidelines, GLP, GCP, GMP and GDP)
Requirements :
Powered by JazzHR
KWhojlTGLh