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Remote Biotech Regulatory Affairs Jobs in Decatur, GA

InspireMD

Field Clinical Specialist

Atlanta, GA · Remote

$75K - $81K/yr

Field Clinical Specialist Remote/Field role InspireMD is a dynamic growing company focused on ... Collaborate with Clinical Affairs to provide outstanding case support for clinical trials, as ...

Deloitte

System Test and Validation Lead

Atlanta, GA · On-site +1

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... This compensation range is specific to a remote role and takes into account the wide range of ...

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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 Aug 17, 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 is a remote biotech regulatory affairs professional?

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 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 popular job titles related to Remote Biotech Regulatory Affairs jobs in Decatur, GA?

For Remote Biotech Regulatory Affairs jobs in Decatur, GA, the most frequently searched job titles are:

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.

Associate Director, Corporate Compliance

Oscar Health

Atlanta, GA • Remote

$134K - $176K/yr

Full-time

Medical, PTO

Re-posted 23 hours ago

Oscar Health rating

6.9

Company rating: 6.9 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

257th of 309 rated insurance

Job description

Hi, we're Oscar. We're hiring an Associate Director, Corporate Compliance to join our Corporate Compliance 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 Associate Director, Corporate Compliance is responsible for training, investigating, monitoring, and enforcing, when necessary, programs, policies, and practices to ensure all applicable operational functions are in compliance with federal, state and local regulatory requirements. The Associate Director manages compliance efforts for Oscar's licensed entities delivering Qualified Health Plans (QHPs) in the individual and small group markets. You will work with leadership and the larger Compliance team servicing Oscar and advising on how best to service its third-party QHP clients. You will use as a foundation for a robust and best in class compliance program including, but not limited to, the seven elements of an effective compliance program as published by the Office of the Inspector General (OIG). You will partner with operational leaders to identify compliance risk, implement corrective action plans, and promote a culture of integrity and excellence across the organization.

You will report into the Director, Corporate and Regulatory Compliance.

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: $134,136 - $176,053 per year. You are also eligible for employee benefits, participation in Oscar's unlimited vacation program and annual performance bonuses.

Responsibilities:

  • Lead, mentor, and support the Compliance team across all lines of business, encouraging professional development and advancing institutional compliance knowledge.
  • Support the design, implementation, and continuous improvement of the corporate compliance program to promote an organizational culture of responsibility and accountability.
  • Monitor and interpret federal and state regulations to lead business strategies that exceed industry standards for insurers, tech innovators, and public companies.
  • Lead compliance investigations to assess adherence to obligations, and oversee the development, and monitoring of effective Corrective Action Plans.
  • Develop and manage comprehensive compliance training programs throughout the entire organization.
  • Produce and deliver clear, actionable compliance reports tailored for all organizational levels, including executive leadership and external regulatory bodies.
  • Partner with Risk and Controls to manage regulatory risk sustainably while deploying scalable compliance functions that support Oscar's technology, strategic partners, and business growth.
  • Lead the Compliance team in regulatory implementations and monitoring.
  • TEFCA subject matter expert
  • Compliance with all applicable laws and regulations
  • Other duties as assigned

Requirements:

  • 7+ years' experience in a healthcare compliance setting, specifically in healthcare compliance, regulatory affairs, or other related experience.
  • 5+ years' experience in managing effective Compliance teams.
  • 5+ Experience applying state and federal health insurance statutes, regulations, marketplace, and MA requirements to meet reporting and audit obligations

Bonus points:

  • Operational or internal audit experience
  • Enterprise risk management experience
  • HIPAA Security experience
  • Experience in a start-up and/or health tech environment

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