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Remote Biotech Regulatory Affairs Jobs in Decatur, GA

Oscar Health

Analyst, Regulatory Affairs

Atlanta, GA · Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ...

Oscar Health

Analyst, Regulatory Affairs

Atlanta, GA · Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first ... This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote ...

LabAnswer

LIMS SME/Business Analyst

Atlanta, GA · Remote

... Regulatory Affairs (ORA). The duties for this position is as follows: Work with end users and ... This is a remote position so the candidate can live anywhere in the USA. The position will require ...

LivaNova

Regulatory & Clinical Specialist

Atlanta, GA · Remote

$85K - $95K/yr

... affairs or a Ph.D. with at least 3 years of experience Location & Travel Requirements ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

PrizePicks

VP, State Government Affairs

Atlanta, GA · On-site +1

$220K - $275K/yr

Anticipate evolving regulatory trends, influencing policy outcomes before they crystallize, and ... S. and are willing to consider remote candidates. #LI-Remote Working at PrizePicks: The typical ...

LivaNova

Director - Product Security

Atlanta, GA · On-site +1

$224K - $234K/yr

Houston, TX is the ideal location for this role, but this is open to Remote opportunities for well ... Partner with R&D, Engineering, Quality, Regulatory Affairs, and Legal teams to embed security ...

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Remote Biotech Regulatory Affairs information

See Decatur, GA salary details

$18

$38

$61

How much do remote biotech regulatory affairs jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for remote biotech regulatory affairs in Decatur, GA is $38.63, according to ZipRecruiter salary data. Most workers in this role earn between $30.96 and $45.77 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Biotech Regulatory Affairs professional, and why are they important?

To thrive as a Remote Biotech Regulatory Affairs professional, you need a strong background in biological sciences or related fields, regulatory knowledge, and experience with drug or device development, often supported by a relevant degree or advanced certification such as RAC. Familiarity with regulatory submission systems (e.g., eCTD), FDA/EMA guidelines, and document management platforms is essential. Exceptional attention to detail, written communication, and cross-functional collaboration skills set standout professionals apart in this field. These competencies ensure regulatory compliance, smooth product approvals, and effective coordination across global teams in a highly regulated environment.

What is the difference between Remote Biotech Regulatory Affairs vs Remote Biotech Quality Assurance?

AspectRemote Biotech Regulatory AffairsRemote Biotech Quality Assurance
Primary FocusRegulatory compliance, submissions, and interactions with authoritiesProduct quality, standards, and process validation
Required CredentialsLife sciences degree, regulatory certifications (e.g., RAC)Life sciences degree, quality management certifications (e.g., CQE)
Work EnvironmentCollaborates with regulatory agencies, cross-functional teamsWorks with manufacturing, quality control, and validation teams
Industry UsageCommon in biotech, pharma, and medical device companiesPrevalent in biotech, pharma, and manufacturing sectors

Remote Biotech Regulatory Affairs focuses on ensuring products meet regulatory standards and managing agency submissions, while Remote Biotech Quality Assurance emphasizes maintaining product quality and compliance through internal processes. Both roles require similar credentials and often collaborate but serve distinct functions within biotech companies.

What are Remote Biotech Regulatory Affairs professionals?

Remote Biotech Regulatory Affairs professionals are specialists who ensure that biotechnology products and processes comply with all relevant regulations and laws. Working remotely, they manage documentation, submissions, and communications with regulatory agencies to facilitate product approvals. They play a key role in keeping companies compliant with evolving guidelines, such as those from the FDA or EMA, while working from locations outside traditional offices. Their work ensures that new biotech products are safe, effective, and legally marketable.

How does a Remote Biotech Regulatory Affairs professional typically collaborate with cross-functional teams while working offsite?

In a remote Biotech Regulatory Affairs role, professionals frequently interact with teams such as research, clinical, quality assurance, and legal through virtual meetings and collaborative platforms. Regular communication is essential to coordinate submission timelines, ensure documentation accuracy, and address regulatory concerns promptly. Successful remote professionals are adept at using project management tools and maintaining proactive communication to bridge any gaps caused by physical distance. This collaborative approach helps ensure that regulatory requirements are met efficiently and that projects progress smoothly.
What job categories do people searching Remote Biotech Regulatory Affairs jobs in Decatur, GA look for? The top searched job categories for Remote Biotech Regulatory Affairs jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Remote Biotech Regulatory Affairs jobs? Cities near Decatur, GA with the most Remote Biotech Regulatory Affairs job openings:
Remote Biotech Regulatory Affairs jobs near you
Infographic showing various Remote Biotech Regulatory Affairs job openings in Decatur, GA as of June 2026, with employment types broken down into 1% As Needed, 42% Full Time, 42% Part Time, 1% Temporary, and 14% Contract. Highlights an 48% Physical, 3% Hybrid, and 49% Remote job distribution, with an average salary of $80,359 per year, or $38.6 per hour.
Analyst, Regulatory Affairs

Analyst, Regulatory Affairs

Oscar Health

Atlanta, GA • Remote

$28.30 - $37.15/hr

Other

Medical, PTO

Posted 9 days ago

Oscar Health rating

6.9

Company rating: 6.9 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

247th of 298 rated insurance

Job description

Hi, we're Oscar. We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team.

Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on serving our members. We started Oscar in 2012 to create the kind of health insurance company we would want for ourselves-one that behaves like a doctor in the family.

About the role:

The Analyst, Regulatory Affairs is a contributor and navigator who coordinates Regulatory Affairs work within the Evidence of Coverage team. You will coordinate large-scale, workgroups and contributes to annual QHP filings. You will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager.

You will report into the Regulatory Manager.

Work Location: This is a remote position, open to candidates who reside in: Atlanta, GA. You will be fully remote; however, our approach to work may adapt over time. Future models could potentially involve a hybrid presence at the hub office associated with your metro area. #LI-Remote

Pay Transparency: The base pay for this role is: $28.30 - $37.15 per hour. You are also eligible for employee benefits and monthly vacation accrual at a rate of 15 days per year.

Responsibilities:

  • Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods
  • Resolve low risk state objections
  • Project manages and implements the internal tracking and monitoring of Regulatory Affairs team deliverables related to our Legislative processes.
  • Coordinate internal working groups by scheduling meetings, intaking requests and ensuring the appropriate people are in the room
  • Prepare agendas, track action items, and follow-ups to ensure timely completion.
  • Maintain comprehensive documentation of regulatory objections, statespecific requirements, and reasons for deviations from standard policy.
  • Escalate issues or delays to leadership
  • Compliance with all applicable laws and regulations.
  • Other duties as assigned.

Requirements:

  • A bachelor's degree in a legal, healthcare-related or humanities field, or 4 years commensurate experience.
  • 2+ years of experience in health insurance customer service, claims, appeals, or Regulatory team
  • Strong attention to detail with the ability to manage complex documentation.

Bonus points:

  • Familiarity with health insurance operations
  • Experience with the individual market health insurance plans
  • Experience working with attorneys and internal stakeholders.
  • Proficiency in MS Office and Google Tools.

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