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.

Global Labeling Lead

Boston, MA
2 weeks 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
2 weeks ago
Audit & Compliance
Pharmacovigilance
Project Management
Ergomed
Full-Time
Experienced

Regulatory & Pharmacovigilance Senior Specialist

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

Data Solutions Coordinator (Regulatory Intelligence)

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

Senior Pharmacovigilance Licensing Manager

London, United Kingdom
1 month ago
Negotiation
Pharmacovigilance
Regulatory Affairs
Sobi
Full-Time
Senior Manager

Executive Director, Safety & Pharmacovigilance

Remote
1 month ago
Cell And Gene Therapy
Drug Safety
Pharmacovigilance
Kyverna Therapeutics
Full-Time
Senior Manager
YEAR $365000 - $390000

Regulatory & Pharmacovigilance Specialist (2-year FTC)

Sarajevo, Bosnia & Herzegovina
2 months ago
Pharmacovigilance
Project Management
Regulatory Affairs
Ergomed
Contractor
Experienced

Senior Director, Clinical Development

Milan, Italy
3 months ago
Clinical Development Strategy
Clinical Trial Design
Medical Monitoring
Sobi
Full-Time
Senior Manager

Senior Manager – Regulatory Affairs & Scientific

London, United Kingdom
4 months ago
Cosmetics/Chemicals Regulatory Services
EU/UK/US Regulatory Frameworks
Regulatory Affairs
J.S. Held LLC
Full-Time
Senior Manager

Senior Specialist, Regulatory & PV Network

Prague, Czech Republic
4 months ago
ICH GCP/GVP
Pharmacovigilance
Project Management
Ergomed
Full-Time
Experienced

LCPPV/LCPRA - English & German

Frankfurt am main, Germany
4 months ago
ADR Reporting
ICH GVP
Pharmacovigilance
Ergomed
Full-Time
Experienced

Director, Government Affairs & Public Policy Lead, Canada

Toronto, Canada
4 months ago
Government Affairs
Policy Analysis
Public Policy
ServiceNow
Full-Time
Manager

Associate Human Health Diagnostics Regulatory Affairs

Kalamazoo, MI
4 months ago
510(k) Submissions
FDA Compliance
IVDR Compliance
Eurofins
Full-Time
Experienced

Associate Director, Regulatory Affairs

Waltham, MA
4 months ago
FDA Submissions
Oncology Drug Development
Pharmaceutical Regulatory
Deciphera Pharmaceuticals
Full-Time
Manager
YEAR $162200 - $223000

Manager, Regulatory Affairs

USA
4 months ago
Compliance
Cross-functional Collaboration
Health Insurance Regulations
Harbor Health
Full-Time
Manager
YEAR $140000 - $165000

Local Contact Person - Pharmacovigilance & Regulatory

Zagreb, Croatia
5 months ago
ADR Reporting
ICH GVP
Pharmacovigilance
Ergomed
Full-Time
Experienced

LCPPV/LCPRA - English & German

Belgrade, Serbia
5 months ago
ADR Reporting
ICH GVP
Pharmacovigilance
Ergomed
Full-Time
Experienced

Regulatory Officer

Mexico City, Mexico
6 months ago
Clinical Trial Submissions
Communication
Detail-Oriented
PSI CRO
Full-Time
Experienced

Local Contact Person - Pharmacovigilance & Regulatory Affairs

Zagreb, Croatia
6 months ago
ADR Reporting
ICH GVP
Pharmacovigilance
Ergomed
Full-Time
Experienced

Director, California Regulatory Affairs (Hybrid Remote)

Folsom, CA
7 months ago
Electric Utility Knowledge
Policy Administration
Regulatory Affairs
California ISO
Full-Time
Manager
YEAR $196875 - $328125

Senior Regulatory Affairs Specialist - International

Palo Alto, CA
7 months ago
IVD
Project Management
Regulatory Affairs
Guardant Health
Full-Time
Experienced
YEAR $112400 - $154550

Senior Regulatory Affairs Manager - Oncology

Palo Alto, CA
7 months ago
Cross-functional Coordination
FDA Regulatory Submissions
IVD/CDx Development
Guardant Health
Full-Time
Senior Manager
YEAR $174300 - $239600

Senior Regulatory Affairs Manager - Screening

Palo Alto, CA
7 months ago
Cross-functional Coordination
FDA Regulatory Submissions
IVD Regulatory Submissions
Guardant Health
Full-Time
Senior Manager
YEAR $174300 - $239600

Senior Regulatory Affairs Manager

Palo Alto, CA
7 months ago
Cross-functional Coordination
FDA Regulatory Submissions
IVD Regulatory Knowledge
Guardant Health
Full-Time
Senior Manager
YEAR $174300 - $239600

Regulatory Affairs Thought Leader

Lancaster, PA
7 months ago
Client Communication
FDA Regulations
ISO Standards
Eurofins
Full-Time
Experienced

LCPPV/LCPRA (English & German)

Zagreb, Croatia
7 months ago
Microsoft Office Applications
Pharmacovigilance
Regulatory Affairs
Ergomed
Full-Time
Experienced

LCPPV/LCPRA - English & Dutch languages required

Guildford, United Kingdom
7 months ago
ADR Reporting
ICH GVP
Microsoft Office Applications
Ergomed
Full-Time
Experienced

LCPPV/LCPRA - English & German

Munich, Germany
7 months ago
English And German Proficiency
ICH GVP
Microsoft Office
Ergomed
Full-Time
Experienced

Regulatory Affairs Senior Specialist/Manager

Worldwide
8 months ago
Clinical Study Management
Global Project Management
ICH GCP/GVP
Ergomed
Full-Time
Experienced

Local Contact Person - Pharmacovigilance & Regulatory

Zagreb, Croatia
8 months ago
ADR/ICSR Management
ICH GVP
Pharmacovigilance
Ergomed
Full-Time
Experienced

Looking for a specific job?