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Remote Fda Jobs in Raleigh, NC (NOW HIRING)

Allucent

Director, Clinical Pharmacology

Cary, NC · Remote

We are looking for a Director, Clinical Pharmacology to join our A-team (office-based*/remote). As ... FDA briefing packages, and other clinical and regulatory documents. Requirements To be successful ...

Allucent

Director, Clinical Pharmacology

Cary, NC · On-site +1

We are looking for a Director, Clinical Pharmacology to join our A-team (office-based*/remote). As ... FDA briefing packages, and other clinical and regulatory documents. Requirements To be successful ...

Allucent

Director, Clinical Pharmacology

Cary, NC · Remote

We are looking for a Director, Clinical Pharmacology to join our A-team (office-based*/remote). As ... FDA briefing packages, and other clinical and regulatory documents. Requirements To be successful ...

Valspec

QA Consultant

Holly Springs, NC · Remote

Remote Employment Type: Contract / Consulting (6-12+ months) Start Date: ASAP About the Role: We ... Ensure compliance with FDA, cGMP, GAMP 5, and 21 CFR Part 11 requirements * Partner with Automation ...

Norstella

Sales Director

Raleigh, NC · Remote

$110K - $140K/yr

MMIT Location: Remote, United States Date Posted: Mar 4, 2026 Employment Type: Full Time ... the FDA, and payers. By providing critical proprietary data supporting AI‐driven workflows ...

CPC

Clinical Trials Project Manager II - remote

Raleigh, NC · Remote

$72K - $95K/yr

Thorough knowledge of the Good Clinical Practice guidelines and applicable FDA and ICH regulations ... Flexible and remote work schedules available for certain positions Visit our web site to learn more ...

Norstella

Legal Counsel

Raleigh, NC · On-site +1

$120K - $150K/yr

Remote, United States Date Posted: Mar 13, 2026 Employment Type: Full Time Job ID: R-1737 ... the FDA, and payers. By providing critical proprietary data supporting AI‐driven workflows ...

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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 May 31, 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 job?

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 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 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.
More about Remote Fda jobs
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 May 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 100% Remote job distribution, with an average salary of $85,679 per year, or $41.2 per hour.

Doc Review Specialist I - US Remote based

Fortrea

Durham, NC • Remote

$55K - $65K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

43rd of 56 rated research

Job description

Doc Review Specialist I - US

Joining Fortrea as a Document Review Specialist I today and you will have a rewarding career, a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team.

The Document Review Specialist I role is responsible for reviewing Investigator Packages, Informed Consent Forms and Advertisements following project & country specific regulations as well as ICH-GCP, FDA and other regional guidance. Document Review Specialist I is responsible for reviewing revised protocols & core ICF's.

This is full time, remote exempt opportunity based in US.

Key / Core Responsibilities

Review Initial/Amended Investigator Packages to assure compliance with regulatory
requirements before granting regulatory green light to a site to start enrolling patients into the clinical trial.

Review Core/Country/Site Informed Consent Form to assure compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Review Patient Recruiting materials (Advertisements) to assure compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Review Investigator Package Plans that document the required quality of documents
included in Investigator Packages following the available SOP with manager oversight.

Review protocol amendment to reconfirm completeness and to assure compliance with Good Clinical Practice (GCP) guidelines.

Review revised Core Informed Consent Forms to reconfirm compliance with sponsor requirements, local regulatory requirements, and Good Clinical Practice (GCP) guidelines Provide input for Corrective and Preventative Actions (CAPAs) related to Document Review activities including Informed Consent Form Review, Patient Recruiting material Review and Investigator Package Review.

And all other duties as needed or assigned.

Required Qualifications

Education:

University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology).
Fluent in English, both written and verbal.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience:

Strong knowledge of ICH, FDA, IRB/IEC and other applicable regulations/guidelines.
2 years' work experience in clinical research Training Lower-level staff

Work Environment

  • Work is performed in an office environment with exposure to electrical office equipment.
  • Occasional drives to site locations with occasional travel both domestic and international.

Physical Requirements:

Frequently stationary for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Regular and consistent attendance.
Varied hours may be required.

Pay Range: USD $55,000-$65,000

Benefits: All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Flexible time off (FTO).

Application Deadline: June 2, 2026

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