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Full Time Non Clinical Slp Jobs in Raleigh, NC (NOW HIRING)

MMS

Senior Nonclinical Writer (US)

Raleigh, NC · On-site

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, 1st ...

hopebridge

Speech Language Pathologist (SLP)

Apex, NC · On-site

$38 - $56/hr

... clinical excellence are at the heart of everything we do. Our multidisciplinary model brings ... No non-compete agreements * Ongoing mentorship, Grand Rounds, and CF supervision Responsibilities ...

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Full Time Non Clinical Slp information

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$43

$65

How much do full time non clinical slp jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for full time non clinical slp in Raleigh, NC is $43.01, according to ZipRecruiter salary data. Most workers in this role earn between $36.68 and $49.52 per hour, depending on experience, location, and employer.

What is a full time non clinical speech-language pathologist (SLP)?

Full Time Non Clinical SLPs are speech-language pathologists who work in roles outside of direct patient care, such as research, education, administration, consulting, or corporate positions. Unlike clinical SLPs who diagnose and treat communication disorders, non-clinical SLPs may develop training materials, conduct research, manage programs, or work in industries like healthcare technology or insurance. These roles utilize the expertise of SLPs without direct therapeutic interaction with clients, offering alternative career paths for those with a speech-language pathology background.

What are the key skills and qualifications needed to thrive as a full time non clinical speech-language pathologist (SLP), and why are they important?

To excel as a Full Time Non Clinical SLP, you need a master's degree in speech-language pathology, ASHA certification (CCC-SLP), and a strong understanding of communication disorders and evidence-based practices. Familiarity with data analysis tools, learning management systems, or research software is often required, depending on the specific non-clinical setting (e.g., education, research, administration). Strong organizational, communication, and problem-solving skills enable effective collaboration, project management, and contribution to program development. These competencies are essential for driving organizational goals, supporting teams, and advancing best practices beyond direct patient care.

What are some common challenges faced by full time non clinical speech-language pathologists (SLPs), and how can they be addressed?

Full Time Non Clinical Speech-Language Pathologists (SLPs) often encounter challenges such as adapting to roles outside direct patient care, including administrative, research, or educational responsibilities. Transitioning from clinical to non-clinical settings may require developing new skills in data analysis, project management, or policy advocacy. Success in these roles typically involves proactive communication, ongoing learning, and effective collaboration with multidisciplinary teams. Staying current with industry trends and seeking mentorship from experienced non-clinical SLPs can also help ease the transition and support long-term career growth.

What is the difference between Full Time Non Clinical Slp vs Speech-Language Pathologist (SLP)?

AspectFull Time Non Clinical SLPSpeech-Language Pathologist (SLP)
CredentialsMaster's degree in Speech-Language Pathology, state licensure, ASHA certificationMaster's degree in Speech-Language Pathology, state licensure, ASHA certification
Work EnvironmentEducational settings, telepractice, research, or administrative rolesHospitals, clinics, schools, private practice
Employer & Industry UsageEducational institutions, telehealth companies, research organizationsHealthcare facilities, schools, private practices

Full Time Non Clinical SLPs focus on roles outside direct patient care, such as research, telepractice, or administrative positions, while traditional SLPs typically work directly with clients in clinical settings. Both roles require similar credentials but differ mainly in work environment and job focus.

What are the most commonly searched types of Non Clinical Slp jobs in Raleigh, NC?

The most popular types of Non Clinical Slp jobs in Raleigh, NC are:

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For Full Time Non Clinical Slp jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Full Time Non Clinical Slp jobs in Raleigh, NC look for?

The top searched job categories for Full Time Non Clinical Slp jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Full Time Non Clinical Slp jobs?

Cities near Raleigh, NC with the most Full Time Non Clinical Slp job openings:

Full Time Non Clinical Slp jobs near you

Senior Nonclinical Writer (US)

MMS

Raleigh, NC • On-site

Full-time

Posted 20 days ago

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, 1st Edition 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 submission documents for INDs/CTAs/NDAs/BLAs/MAAs, 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:

  • BS + 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.
  • 5+ 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.

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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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