Regulatory Affairs Remote Jobs

Find remote jobs requiring Regulatory Affairs skills. Apply now and work from anywhere.

Regulatory Affairs refers to the work of making sure products follow laws and safety rules from development to market. Professionals in this field translate complex regulations into clear plans so products can be approved and kept compliant.

Day to day, the role often includes preparing regulatory submissions, writing technical documents, tracking changes in law, and answering questions from regulators. It also involves coordinating across teams to ensure labeling, manufacturing, and quality systems meet required standards.

This skill suits remote work because much of the work is document based and can be handled online. Submissions, reports, and correspondence move through digital systems. Remote teams can review filings, run virtual meetings with experts, and manage timelines across time zones.

Industries that rely on Regulatory Affairs include

  • Pharmaceuticals and biotech
  • Medical devices and diagnostics
  • Healthcare software and digital health
  • Food, cosmetics, and consumer products
  • Chemical and environmental sectors
  • Regulatory consulting firms

To build this skill, start by learning the regulations relevant to your region and product type and practice writing clear regulatory documents. Take courses or certifications in regulatory affairs and regulatory writing. Gain experience by supporting submissions or quality processes and seek feedback from experienced colleagues. Keep up with regulatory updates, join professional networks, and develop strong written communication and project management habits for remote collaboration.

Food Regulatory Advisor

United Kingdom
5 days ago
Food Legislation
Label Compliance
Quality Assurance
SGS
Full-Time
Experienced
YEAR $45600 - $45600

Head of Global GxP Quality System and Compliance

Stockholm, Sweden
1 week ago
GxP Compliance
Leadership
Quality Management Systems
Sobi
Full-Time
Senior Manager

Study Start Up Specialist

Raleigh, NC
1 week ago
Clinical Research
ICH-GCP
Project Management
Ergomed
Full-Time
Experienced

Study Start Up Specialist

Raleigh, NC
2 weeks ago
Clinical Research
ICH-GCP
Project Management
Ergomed
Full-Time
Experienced

Senior Specialist, Regulatory Registration and Compliance

Belgrade, Serbia
2 weeks ago
Marketing Authorization
Pharmaceutical Compliance
Project Management
Ergomed
Full-Time
Experienced

Global Labelling Lead

Prague, Czech Republic
2 weeks ago
Cross-Functional Leadership
Prescription Drug Labeling
Project Management
Sobi
Full-Time
Experienced

Medical Director, Clinical Development (Neurology)

Waltham, MA
3 weeks ago
Clinical Development
Clinical Trial Design
Medical Monitoring
Deciphera Pharmaceuticals
Full-Time
Manager
YEAR $248000 - $341000

Associate Director, Clinical Science

Waltham, MA
3 weeks ago
Clinical Data Analysis
Clinical Development
Hematology-Oncology
Deciphera Pharmaceuticals
Full-Time
Manager
YEAR $171000 - $236000

Regulatory Affairs Specialist

Kuala Lumpur, Malaysia
1 month ago
ISO13485
Medical Device Registration
Regulatory Affairs
Intuitive
Full-Time
Experienced

Senior Specialist, Regulatory Registration and Compliance

Zagreb, Croatia
1 month ago
Marketing Authorization
Pharmaceutical Compliance
Project Management
Ergomed
Full-Time
Experienced

Specialist, Regulatory & PV Delivery

Belgrade, Serbia
1 month ago
Clinical Research
ICH GCP
Pharmacovigilance
Ergomed
Full-Time
Experienced

Pharmacovigilance Licensing Manager

Basel, Switzerland
1 month ago
Alliance Management
Contract Negotiation
Pharmacovigilance
Sobi
Full-Time
Manager

Associate Director, Pharmacovigilance Scientist

Waltham, MA
1 month ago
Aggregate Reporting
Pharmacovigilance
Regulatory Affairs
Deciphera Pharmaceuticals
Full-Time
Manager
YEAR $162000 - $223000

Senior Specialist, Regulatory & PV Network

Warsaw, Poland
1 month ago
ICH GCP
Pharmacovigilance
Project Management
Ergomed
Full-Time
Experienced

Clinical Research Associate II

Australia
1 month ago
Clinical Monitoring
Clinical Trials
ICH-GCP Compliance
I-Pharm Consulting
Full-Time
Experienced

Pharmaceutical Research Specialist

United States
1 month ago
Clinical Trial Design
Data Analysis
Pharmaceutical Research
CuraSenseAI
Other
Experienced

Pharmaceutical & Clinical Research Expert

Worldwide
1 month ago
Biomedical Research
Clinical Research
Pharmaceutical Sciences
CuraSenseAI
Other
Expert

Clinical Research Scientist

Worldwide
1 month ago
Clinical Research
Data Analysis
Protocol Development
STEM Sync AI
Contractor
Expert
HOUR $80 - $150

Pharmaceutical & Clinical Research Expert

United States
1 month ago
Biomedical Research
Clinical Research
Medical Evaluation
CuraSenseAI
Other
Expert

Head of Government Affairs

Fort Mill, SC
1 month ago
Communication
Government Affairs
Public Policy
Continental
Full-Time
Senior Manager

Local PV & Regulatory Affairs Contact (LCPPV/LCPRA)

Belgrade, Serbia
2 months ago
Case Handling
ICH GVP
Literature Screening
Ergomed
Full-Time
Experienced

Manager, Regulatory Affairs

Waltham, MA
2 months ago
Cross-functional Collaboration
IND/CTA Submissions
Regulatory Affairs
Deciphera Pharmaceuticals
Full-Time
Manager
YEAR $116000 - $160000

Senior Manager, Government Affairs

Austin, TX
2 months ago
ERCOT Market Design
Government Affairs
Legislative Advocacy
Apex Clean Energy
Full-Time
Senior Manager

Senior Regulatory Affairs Specialist II

Ponte Vedra, FL
2 months ago
Labeling & Promotional Review
Regulatory Affairs
Regulatory Strategy & Risk Assessment
Treace
Full-Time
Experienced

Corporate Counsel

Ann Arbor, Michigan, USA
3 months ago
Compliance
Contract Negotiation
Corporate Governance
May Mobility
Full-Time
Experienced

Specialist, Regulatory & Pharmacovigilance

Guildford, United Kingdom
3 months ago
Pharmacovigilance
Project Management
Regulatory Affairs
Ergomed
Full-Time
Experienced

Global Labeling Lead

Boston, MA
4 months ago
Cross-functional Leadership & Project Management
Global Labeling/CCDS & EU PI
Regulatory Affairs
Sobi
Full-Time
Senior Manager
YEAR $160000 - $195000

Regulatory & Pharmacovigilance Specialist

Guildford, United Kingdom
4 months ago
Audit & Compliance
Pharmacovigilance
Project Management
Ergomed
Full-Time
Experienced

Regulatory & Pharmacovigilance Senior Specialist

Warsaw, Poland
4 months ago
ICH GCP/GVP
Pharmacovigilance
Project Management
Ergomed
Full-Time
Experienced

Data Solutions Coordinator (Regulatory Intelligence)

HSR Layout, Bengaluru, India
4 months ago
Analytical Judgment
Data Structuring
GXP
REDICA Systems
Full-Time
Experienced

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