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Remote Fda Jobs in Raleigh, NC (NOW HIRING)

Valspec

ERP (D365) Validation Consultant

Durham, NC · On-site +1

Ensure D365 deployments meet all relevant regulatory standards, such as FDA 21 CFR Part 11, GxP ... Remote work options * Professional development opportunities * Health and wellness benefits

Valspec

ERP (D365) Validation Consultant

Raleigh, NC · On-site +1

Ensure D365 deployments meet all relevant regulatory standards, such as FDA 21 CFR Part 11, GxP ... Remote work options * Professional development opportunities * Health and wellness benefits

Danaher

Principal Clinical Scientist

Raleigh, NC · On-site +1

... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA ...

Danaher

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

... FDA guidance, EU GMP Annex 15, and lifecycle approach. * Lead the planning, execution, and ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Senior Engineer, Process Validation

Raleigh, NC · On-site +1

$100K - $130K/yr

... FDA guidance, EU GMP Annex 15, and lifecycle approach. * Lead the planning, execution, and ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

M3USA

Participant Recruitment Analyst

Raleigh, NC · Remote

This is a remote position. The Participant Recruitment Analyst will be responsible for analyzing ... Maintain compliance with HIPAA, FDA, GCP, IRB guidelines, and M3 Wake Research SOPs * Review ...

COMPASS Pathways

HEOR Science Liaison

Raleigh, NC · On-site +1

Food and Drug Administration (FDA), as well as Innovative Licensing and Access Pathway (ILAP ... Location: Remote in the United States. Reports to: Director, HEOR. Roles and responsibilities ...

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Showing results 21-39

All JobsFda JobsRemote Fda JobsRemote Fda Jobs in Raleigh, NC

Remote Fda information

See Raleigh, NC salary details

$25.1K

$85.7K

$168.7K

How much do remote fda jobs pay per year?

As of Sep 6, 2026, the average yearly pay for remote fda in Raleigh, NC is $85,679.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,778.00 and $111,156.00 per year, depending on experience, location, and employer.

What is a remote FDA?

A Remote FDA job typically involves working for or with the U.S. Food and Drug Administration (FDA) from a remote location. These roles can include regulatory affairs, compliance, medical writing, research, and reviewing submissions for drug and medical device approvals. Remote FDA jobs require knowledge of FDA regulations, strong analytical skills, and experience in healthcare, pharmaceuticals, or related fields. They offer flexibility while maintaining high regulatory standards and ensuring public health and safety.

What are the typical daily responsibilities of a remote FDA compliance specialist?

A Remote FDA Compliance Specialist generally reviews and updates regulatory documents, conducts virtual audits, and monitors company practices for FDA compliance. They regularly collaborate with cross-functional teams, such as quality assurance, legal, and product development, to provide guidance on regulatory requirements and respond to compliance queries. Additionally, they prepare and submit necessary reports, maintain records for inspections, and stay current on evolving regulations. This remote structure allows flexibility but also demands excellent organization, communication, and self-discipline to ensure all deadlines and compliance standards are met.

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

To excel as a Remote FDA Compliance Specialist, you need in-depth knowledge of FDA regulations, quality assurance procedures, and a background in life sciences or a related field. Proficiency in using compliance management systems, electronic document management tools, and relevant certifications such as RAC (Regulatory Affairs Certification) are often required. Exceptional attention to detail, self-motivation, and strong written and verbal communication skills are vital for remote collaboration and thorough documentation. These abilities ensure regulatory adherence, minimize compliance risks, and facilitate effective remote teamwork within the pharmaceutical or medical device industry.

What jobs can I do completely remotely as a remote FDA?

A remote FDA typically refers to a Food and Drug Administration-related role that can be performed remotely, such as regulatory affairs specialists, quality assurance managers, or compliance analysts. These positions often require knowledge of regulations, strong communication skills, and familiarity with digital tools for document review and reporting, allowing work to be done entirely online. However, some roles may require occasional on-site visits or inspections depending on the specific job and employer policies.

What are the most commonly searched types of Fda jobs in Raleigh, NC?

The most popular types of Fda jobs in Raleigh, NC are:

What are popular job titles related to Remote Fda jobs in Raleigh, NC?

For Remote Fda jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Remote Fda jobs in Raleigh, NC look for?

The top searched job categories for Remote Fda jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Remote Fda jobs?

Cities near Raleigh, NC with the most Remote Fda job openings:

Remote Fda jobs near you
Infographic showing various Remote Fda job openings in Raleigh, NC as of August 2026, with employment types broken down into 59% Full Time, and 41% Part Time. Highlights an 100% Remote job distribution, with an average salary of $85,679 per year, or $41.2 per hour.

Senior Statistician - UK/Europe - Remote

Worldwide Clinical Trials

Durham, NC • Remote

$84K - $103K/yr

Full-time

Posted 3 days ago

New

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the Senior Statistician does at Worldwide

Independently manages statistical project support and provides expert statistical consultancy across the stats function.
What you will do

  • Manage the statistics support to one or more projects/sponsor programs of work, ensuring that needs are met by expert and timely statistical consultancy and support

  • Provides expert review of study designs, analysis plans, and reports

  • Assist sponsors in the design of clinical trials, including statistical sections of the study protocol, randomization methodology, and writing statistical analysis plans

  • Consult with internal departments, sponsors, and other third parties regarding statistical issues and reporting requirements

  • Provide project support to the statistics reporting process through the specification/review of tables, figures, and listings shells, writing/review of derived dataset specifications, and the formatting of report documents and tabulations

  • Undertake the preparation of final reports, including the production of tables, listings, and figures, and report writing

  • Develop, evaluate, and run Statistical Analysis System (SAS) programs for the statistical analysis and reporting of clinical study data. This includes programs for derived datasets, Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation Model (SDTM), and Analysis Data Model (ADaM) datasets, tables, figures, and listings, and their validation

  • Ensure the maintenance of documentation, e.g., the description of programs and validation

  • Produce ad hoc data summaries when requested during a trial.
    Extract information from the system during a trial, e.g., summaries, data listings, study data sets.

  • Validate software, in the role of system owner or tester, and test SAS Macros, maintaining the required validation and testing documentation

  • Make statistical contributions to manuscripts for publication/presentation

  • Provide support for the bidding process, including contribution to budget review, proposals, and bid defense meetings

  • Lead the identification of system and process improvements, and develop and implement solutions to improve the efficiency and quality of clinical study data processing and reporting

  • Support the development of statistical design and analysis policies

  • Maintain knowledge in design consultancy and analysis methodology, statistical software packages (e.g., SAS and nQuery), and regulatory guidance documents, e.g. International Council for Harmonization (ICH), Food and Drug Administration (FDA), and Committee for Medicinal Products (CPMP) points to consider

  • Assist with Quality Assurance and Audit requirements

  • Assist the Director of Biostatistics with all other aspects of the job as required

  • Perform all activities in compliance with Worldwide Clinical Trials and agreed sponsor quality system standards, relevant ICH standards, and specifically with FDA Quality System Regulation (including 21CFR Part 11)

  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.


What you bring to the role:

  • Computer literate and numerate with a proven ability to adapt to various computer systems

  • Expert-level project statistician experienced in providing statistical leadership to projects

  • Design and analysis consultancy skills and knowledge across a broad range of applications, together with key competencies in customer focus, delivering on commitments, building strong relationships, communicating, influencing, and embracing innovation and change

Your experience

  • Master's level in mathematics, statistics, or another subject required with a strong statistical component

  • Minimum 3 years of statistical experience leading clinical trial projects and data analysis

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

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