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Remote Nuclear Safety Analyst Jobs in Raleigh, NC

DAN

Safety Services Specialist

Durham, NC · On-site +1

This position requires full-time, office based work and is not eligible for remote or hybrid ... Monitor and analyze safety trends within the dive industry to provide input into program ...

ClinDCast LLC

Epic ClinDoc Analyst

Cary, NC · Remote

Knowledge of clinical informatics, healthcare compliance, and patient safety best practices. * Strong analytical, problem-solving, and communication skills. This is a remote position.

IQVIA

Inside Sales Representative

Raleigh, NC · Remote

Analyze territory trends and customer insights to identify opportunities for increased engagement ... Remote Work Environment * Career Growth and Professional Development Opportunities Required ...

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Remote Nuclear Safety Analyst information

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$38

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How much do remote nuclear safety analyst jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for remote nuclear safety analyst in Raleigh, NC is $38.10, according to ZipRecruiter salary data. Most workers in this role earn between $30.87 and $43.70 per hour, depending on experience, location, and employer.

What is the difference between Remote Nuclear Safety Analyst vs Remote Nuclear Regulatory Compliance Specialist?

AspectRemote Nuclear Safety AnalystRemote Nuclear Regulatory Compliance Specialist
Required CredentialsEngineering degree, safety certificationsEngineering or legal background, compliance certifications
Work EnvironmentResearch facilities, safety departmentsRegulatory agencies, compliance departments
Industry UsagePower plants, nuclear facilitiesRegulatory bodies, nuclear industry
Common Search IntentSafety analysis, risk assessmentRegulatory compliance, legal standards

The Remote Nuclear Safety Analyst primarily focuses on evaluating safety protocols and risk assessments within nuclear facilities, ensuring operational safety. In contrast, the Remote Nuclear Regulatory Compliance Specialist concentrates on adhering to legal and regulatory standards set by authorities. Both roles require specialized knowledge and certifications but differ in their core responsibilities and work environments.

What are the main challenges faced by a Remote Nuclear Safety Analyst, and how can they be addressed?

A key challenge for Remote Nuclear Safety Analysts is ensuring thorough communication and collaboration with on-site teams, as safety assessments often require detailed, up-to-date information from the facility. To address this, it's important to establish strong virtual communication channels, participate in regular video meetings, and use secure data-sharing platforms. Additionally, remote analysts must stay current on regulatory changes and best practices by actively engaging in professional development and networking with industry peers. Proactively seeking feedback and clarifying expectations with on-site staff can also help mitigate misunderstandings and ensure robust safety oversight.

What are the key skills and qualifications needed to thrive as a Remote Nuclear Safety Analyst, and why are they important?

To excel as a Remote Nuclear Safety Analyst, you need a strong background in nuclear engineering or physics, a thorough understanding of safety regulations, and experience with risk assessment. Familiarity with tools such as probabilistic safety assessment (PSA) software, industry-specific modeling programs, and certifications like Certified Safety Professional (CSP) are often required. Exceptional analytical thinking, attention to detail, and clear communication are crucial for interpreting data and collaborating with remote teams. Mastering these skills ensures accurate safety evaluations, regulatory compliance, and effective risk mitigation in the nuclear industry.

What is a Remote Nuclear Safety Analyst?

A Remote Nuclear Safety Analyst is a professional who evaluates and monitors the safety protocols and procedures of nuclear facilities or projects while working from a remote location. They analyze data, assess compliance with regulations, and help ensure that nuclear operations are conducted safely to protect people and the environment. This role often involves reviewing technical documents, preparing safety reports, and providing recommendations for risk mitigation. Remote Nuclear Safety Analysts use specialized software and collaborate with onsite teams to maintain high safety standards without being physically present at the nuclear site.
What are popular job titles related to Remote Nuclear Safety Analyst jobs in Raleigh, NC? For Remote Nuclear Safety Analyst jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Remote Nuclear Safety Analyst jobs in Raleigh, NC look for? The top searched job categories for Remote Nuclear Safety Analyst jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Nuclear Safety Analyst jobs? Cities near Raleigh, NC with the most Remote Nuclear Safety Analyst job openings:
Remote Nuclear Safety Analyst jobs near you
Infographic showing various Remote Nuclear Safety Analyst job openings in Raleigh, NC as of July 2026, with employment types broken down into 87% Full Time, 8% Part Time, 1% Temporary, and 4% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $79,241 per year, or $38.1 per hour.

FSP Principal Biostatistician, Safety Analytics

IQVIA

Durham, NC • Remote

Full-time

Re-posted 27 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

61st of 230 rated it services

Job description

Job: FSP Principal Biostatistician, Safety Analytics

Location: Home-based in the U.S. or Canada

Why DSSS?

Data Sciences Staffing Solutions, DSSS, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This yields all the benefits of working for an industry leading global CRO and collaborating directly with cross-functional sponsor teams. Sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies to market.

Job Summary:

The Principal Biostatistician is responsible for providing statistical support for Phase 1, 2 and 3 pharmaceutical clinical trials in patients, focusing on safety endpoints and outcomes.

Additional Benefits:

  • Home-based remote working opportunities.
  • Work/life balance as well as flexible schedules.
  • Collaborating with motivated, high-performance, statistical and research teams.
  • Technical training and tailored development curriculum.
  • Research opportunities that match your unique skillset.
  • Promising career trajectory.
  • Job stability: long-term engagements and re-deployment opportunities.
  • Focus on bringing new therapies to market rather than project budgets and change orders.
  • Experience with regulatory submissions.
  • Engaging, fast-paced environment.
  • Good work-life balance.

Job Responsibilities:

  • Support Safety Analytics with ADaM/TFL standard development of safety deliverables, including specialty areas such as Hypersensitivity, Injection/Infusion Site Reaction.
  • Support Safety Analytics and the study team on the delivery of Patient Profile display for Hepatic or other areas.
  • Provide ADaM/TFL/interactive package review support for the Safety Analytics team supported portfolio deliveries, including cross-checks between interactive outputs and TFLs.
  • Interrogating root cause of issues identified during ADaM/TFL/Interactive package review
  • Providing statistical leadership and support for safety analyses for Phase 1/2/3 trials.
  • Collaborate with multi-disciplinary project teams to establish project objectives and timelines.
  • Participating in study design discussions, including protocol development
  • Write the statistical sections of clinical trial protocols.
  • Reviewing CRFs, data review guidelines, and related study documentation to ensure statistical and safety considerations are appropriately addressed.
  • Developing and reviewing statistical analysis plans and TFL templates.
  • Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
  • Collaborate with Data Management, Clinical Development, and Clinical Operations with statistical expertise.
  • Contribute to clinical study reports and other regulatory documents, e.g. NDA, DSURs, Briefing Documents, ISS, ISE, etc.
  • Serving as an unblinded DMC statistician across multiple studies, ensuring compliance with sponsor and regulatory requirements.
  • Provide guidance and supervision to programmers in authoring analysis dataset specifications and programming/validation of tables, listings, and figures.
  • Perform exploratory safety analyses
  • Perform validation of analysis variables and statistical outputs
  • Interpret study results and review reports of study results for accuracy.
  • Present, communicate and interpret safety analyses to study teams
  • Support exploratory analyses.
  • Participate in pre-IND or NDA activities.

Qualifications (Minimal acceptable level of education, work experience, and competency)

  • PhD in Statistics, Biostatistics, or related field with 3+ years industry experience.
  • MS in Statistics, Biostatistics, or related field with 5+ years of industry experience.
  • At least 2 years of Phase 1, 2 and 3 clinical trial experience.
  • Strong experience reviewing ADaM datasets and TFLs (standard and customized output review).
  • Ability to follow data specifications and programming specifications and provide clear, actionable review comments.
  • Able to investigate and troubleshoot mismatches between tools/outputs (e.g., Spotfire vs. SAS TFL) by interrogating programs to identify root cause and errors.
  • Strong communication and time management: provide realistic timeline estimates, flag risks/delays early, and ask the right questions to move work forward.
  • R/SAS programming skills
  • Demonstrated ability to work pro-actively and independently.
  • Able to effectively communicate his/her ideas and to manage programmers in a constructive manner.
  • Understanding of ICH GCP, ICH E9 plus general knowledge of industry practices and standards.
  • Experience with CDISC SDTM and CDASH

Desired Experience:

  • Leading DSBM or DMC for biostatistics

#LI-Remote

#LI-NITINMAHAJAN

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $111,000.00 - $309,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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