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Narrative Writer Jobs in Raleigh, NC (NOW HIRING)

Pacer Group

Product Safety Lead

Raleigh, NC · On-site

Enters the report in the safety database, writes comprehensive narrative summaries and conducts follow-up as required. * On Time Submission of AE Reports: Ensures on time submission of individual AE ...

Varsity Tutors

Filmmaking Tutor

Chapel Hill, NC · Remote

$40/hr

Ability to explain shot composition, three-point lighting, narrative structure, continuity editing ... Guides students through writing screenplays, storyboarding scenes, operating cameras, setting up ...

Varsity Tutors

Filmmaking Tutor

Raleigh, NC · Remote

$40/hr

Ability to explain shot composition, three-point lighting, narrative structure, continuity editing ... Guides students through writing screenplays, storyboarding scenes, operating cameras, setting up ...

Varsity Tutors

Filmmaking Tutor

Durham, NC · Remote

$40/hr

Ability to explain shot composition, three-point lighting, narrative structure, continuity editing ... Guides students through writing screenplays, storyboarding scenes, operating cameras, setting up ...

bioMerieux Inc.

Payor Engagement Director

Durham, NC

$215K - $269K/yr

Align on the global and local narrative for payer engagements. Contribute to enhancing the ... Excellent public presentation, verbal and written communication skills tailored to payor needs.

Labcorp

Content Designer

Durham, NC · On-site

Strong storytelling and writing ability with a portfolio showcasing narrative clarity and visual communication * Ability to communicate ideas clearly across teams and to present work effectively in ...

Labcorp

Content Designer

Durham, NC · Hybrid

Strong storytelling and writing ability with a portfolio showcasing narrative clarity and visual communication * Ability to communicate ideas clearly across teams and to present work effectively in ...

Strata Solar LLC

Communications Manager

Durham, NC

... shape narrative around company initiatives * Develop and execute integrated communications ... Create compelling, clear, and accurate communications content across formats (written, video ...

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How much do narrative writer jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for narrative writer in Raleigh, NC is $37.86, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $45.82 per hour, depending on experience, location, and employer.

What is a Narrative Writer job?

A Narrative Writer creates engaging stories for various media, such as video games, films, or interactive experiences. They develop characters, dialogue, and plots to immerse audiences in compelling narratives. This role often involves collaboration with designers, artists, and developers to ensure storytelling aligns with the project's vision. Strong writing skills, creativity, and an understanding of storytelling structures are essential for success in this position.

What are the key skills and qualifications needed to thrive in the Narrative Writer position, and why are they important?

To thrive as a Narrative Writer, you need exceptional storytelling abilities, strong command of language, and experience in creative or content writing, often supported by a degree in English, Creative Writing, or a related field. Familiarity with scriptwriting software, content management systems, and collaborative editing tools is highly valuable. Excellent communication, adaptability, and attention to detail are crucial soft skills for standing out in this position. These abilities enable Narrative Writers to craft engaging narratives that align with project goals and resonate with audiences across various media.

What does a narrative writer do?

A narrative writer creates stories, scripts, or content that convey a compelling and coherent narrative. They often work with storytelling techniques, character development, and plot structure, using tools like writing software and research to produce engaging content for various media such as books, films, or games.

What are the typical day-to-day responsibilities of a Narrative Writer in a professional setting?

As a Narrative Writer, your daily tasks often involve crafting compelling storylines, developing characters, and collaborating closely with teams such as designers, game developers, or marketing professionals. You'll likely participate in brainstorming sessions, draft and revise scripts or story outlines, and ensure the narrative is cohesive across all platforms or deliverables. Regular feedback sessions and adaptation to project needs are common, requiring both creativity and flexibility. This dynamic, collaborative environment offers opportunities to see your storytelling impact multiple aspects of a project and to grow your skills through diverse challenges.

What are popular job titles related to Narrative Writer jobs in Raleigh, NC? For Narrative Writer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Narrative Writer jobs in Raleigh, NC look for? The top searched job categories for Narrative Writer jobs in Raleigh, NC are:
Narrative Writer jobs near you
Product Safety Lead

Product Safety Lead

Pacer Group

Raleigh, NC • On-site

Contractor

Posted 14 days ago

Job description

Job Title: Product Safety Lead
Job Location: Raleigh, NC 27615
Job Duration: 6 months

Shift/ Schedule: 3 days a week (flexible days)
 
Job Summary:
 
  • Responsible for all tasks related to the collection, processing, follow up and regulatory reporting of adverse events (AEs), serious AEs from Clinical Trials (SAEs), adverse events of interest (AEIs) and pregnancy reports for all marketed and investigational products.
  • This position will routinely process all types of reports for all categories of products (medical device, cosmetic and OTC products).  
Job Responsibilities:
  • Post Marketing Adverse Event Processing: Ability to independently analyze and accurately process adverse event reports from all sources, for medical devices, cosmetics and OTCs. This includes an ability to provide an assessment of complex medical information and relevant lab results, and the ability to enter the report in the safety database, write comprehensive narrative summaries, and conduct follow-up for all types of products.
  • Clinical Study SAE Processing: Actively participates in internal clinical project teams and provides input regarding the collection of adverse events during the conduct of Merz Aesthetic clinical studies. Develops and maintains the safety sections of clinical trial protocols and Investigator Brochures (IBs). Writes Safety Management Plans as required. Participates in all safety related end-of-study activities such as SAE reconciliation. Enters the report in the safety database, writes comprehensive narrative summaries and conducts follow-up as required.
  • On Time Submission of AE Reports: Ensures on time submission of individual AE and SAE case reports to worldwide regulatory agencies, partners, and affiliates in accordance with applicable regulations and agreed timelines. Ensures that Merz Aesthetics obligations with respect to Safety Data Exchange Agreements (SDEAs) are fulfilled in an appropriate and timely manner. 
  • Evaluation of Individual AE Reports and Safety Data: Evaluation of individual case reports considering medical/pharmacological aspects as well as verification of MedDRA/IMDRF coding for adverse events (clinical signs), problem codes impact on health, examination findings, cause evaluation. Conducts medical review and assessment on individual AE case reports. Maintains general knowledge of signals, trends, and closely monitored events. Communicates any potential safety issue appropriately. Able to make clinical judgments regarding whether or not an individual report meets clinical/regulatory criteria for expedited submission to Health Authorities.
  • Literature Reviews: Execute, review and document periodic and ad-hoc reviews of the biomedical literature to identify novel or reportable individual safety case reports / safety signals
  • Safety database proficiency: Able to effectively use industry-standard, validated product safety database. Proficiency with data entry, process flow, query and report generating functions are essential. Creates draft reports/data tables to fulfill regulatory agency or notified body queries, or upon request of Merz Aesthetics management. Performs searches of the safety database for internal compliance or other ad hoc queries as required.
  • Review and Update of Departmental documents: Assists in development, review, and implementation of Global Device Vigilance working practices, standard operating procedures (SOPs), or guidance documents to ensure compliance with international regulations governing clinical safety and device vigilance for adverse event reporting.
  • Provides training regarding AE reporting: Provides training to clinical investigators, sales representatives, other employees, and contractors in their obligations regarding adverse event reporting. May assist with orientation/mentoring of new Product Safety staff.
  • Audit Support: Participate in all internal and external audits as needed.
  • Supports Regional Safety / Vigilance: Supports regional, non-US Safety staff as needed to ensure compliance with vigilance requirements in ex-US markets.
  • Collaborate with Other Global Functions: Cooperative interaction with non-Safety representatives across company business units such as Quality, Clinical, Regulatory, and Medical Affairs.
Technical & Functional Skills:
  • Thorough knowledge and experience in all aspects of safety reporting for clinical trials and marketed products – both drugs and medical devices.
  • Strong knowledge and experience with validated safety databases (Argus, ARISg, SIAB, etc.). This also includes MedDRA, WHODrug, and IMDRF coding.
  • Must work effectively/collaboratively in a fast-paced yet efficient team environment with individuals at all levels within an organization.
  • Strong knowledge of FDA and EU regulations governing clinical safety and vigilance.
  • Strong organizational and project management skills.
  • Strong verbal and written communication skills.                                                                                                                       
Minimum Qualifications:
  • Bachelor’s degree in a science or heath care-related field or RN/PharmD
  • 5+ years of experience in drug safety or medical device vigilance (preferred) in an industry setting or equivalent
Preferred Qualifications:
  • Direct health care experience with injectable products highly desired
  • Knowledge and experience with document management systems (EDMS, eTMF, etc.).
  • Experience in vendor management.
  • Demonstrates relationship building and problem-solving skills.