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.

Regulatory Affairs Thought Leader

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

LCPPV/LCPRA (English & German)

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

LCPPV/LCPRA - English & Dutch languages required

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

LCPPV/LCPRA - English & German

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

Regulatory Affairs Senior Specialist/Manager

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

Local Contact Person - Pharmacovigilance & Regulatory

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

Regulatory Affairs Thought Leader

Lancaster, PA
10 months ago
FDA Regulations
Knowledge Of EU MDR/IVDR
Knowledge Of ISO Standards
Eurofins
Full-Time
Experienced

Local Contact Person (LCPPV/LCPRA)

Belgrade, Serbia
10 months ago
ADR Reporting
Pharmacovigilance
Regulatory Affairs
Ergomed
Full-Time
Experienced

LCPPV/LCPRA - English & Portuguese

Lisbon, Portugal
10 months ago
English And Portuguese Proficiency
ICH GVP
Microsoft Office Applications
Ergomed
Full-Time
Experienced

Medical Director/Senior Medical Director

Boston, MA
11 months ago
Clinical Development
Medical Affairs
Regulatory Affairs
Glycomine
Full-Time
Experienced

Senior Regulatory Specialist

Worldwide
11 months ago
FDA Regulations
Medical Devices
Regulatory Affairs
DeepHealth
Full-Time
Senior Manager

Senior Clinical Project Manager

Boston, MA
11 months ago
Clinical Trial Management
CRO Management
Project Management
Glycomine
Full-Time
Senior Manager

Medical Director/Senior Medical Director

Chicago, IL
11 months ago
Clinical Development
Medical Affairs
Medical Strategy
Glycomine
Full-Time
Experienced

Senior Pharmacovigilance Specialist

Waltham, MA
11 months ago
Compliance
Pharmacovigilance
Quality Assurance
Deciphera Pharmaceuticals
Full-Time
Senior Manager

Senior Specialist Pharmacovigilance

Waltham, MA
11 months ago
Audit Readiness
Compliance
Pharmacovigilance
Deciphera Pharmaceuticals
Full-Time
Senior Manager

Local Contact Person Pharmacovigilance

Québec City, Canada
11 months ago
Communication
Compliance
English Proficiency
Ergomed
Full-Time
Experienced

Regulatory Compliance Specialist

King of Prussia, PA
11 months ago
Compliance Reporting
Customer Service
Environmental Compliance
Enviri Corporation
Full-Time
Experienced

Local Contact Person for Pharmacovigilance

Zagreb, Croatia
11 months ago
Communication
Compliance
Microsoft Office
Ergomed
Full-Time
Experienced

Regulatory Compliance Specialist

King of Prussia, PA
11 months ago
Compliance Reporting
Customer Service
Environmental Compliance
Enviri Corporation
Full-Time
Experienced

Local Contact Person for Pharmacovigilance & Regulatory Affairs

Toronto, Canada
11 months ago
Communication
Compliance
English
Ergomed
Full-Time
Experienced

Local Contact Person for Pharmacovigilance

Brussels, Belgium
11 months ago
Communication
Compliance
Microsoft Office
Ergomed
Contractor
Experienced

Director Global Launch Excellence Nephrology

Paris, France
1 year ago
Cross-functional Collaboration
Global Launch
Market Access
Sobi
Full-Time
Manager

Manager, Regulatory & Pharmacovigilance

Zagreb, Croatia
1 year ago
Communication
Leadership
Pharmacovigilance
Ergomed
Full-Time
Manager

Associate Director, Regulatory Affairs

Waltham, MA
1 year ago
Drug Development
IND Filings
Oncology
Deciphera Pharmaceuticals
Full-Time
Manager
YEAR $158000 - $217000

Senior Clinical Research Associate I

Ankara, Turkey
1 year ago
Clinical Trials
Communication
Monitoring
PSI CRO
Full-Time
Experienced

Senior Director, Clinical Development

Woburn, MA
1 year ago
Clinical Trial Management
GCP Compliance
Medical Expertise
Sirtex
Full-Time
Senior Manager
YEAR $253000 - $299000

Senior Specialist Regulatory PV

Belgrade, Serbia
1 year ago
Communication
Pharmacovigilance
Project Management
Ergomed
Full-Time
Senior Manager

Senior Clinical Research Associate

Kuala Lumpur, Malaysia
1 year ago
Clinical Trial Monitoring
Communication
Project Management
PSI CRO
Full-Time
Senior Manager

Senior Medical Director, Medical Affairs

Durham, NC
1 year ago
Clinical Development
Medical Affairs Strategy
Medical Leadership
Glycomine
Full-Time
Expert

Qualified Person Responsible for Pharmacovigilance (QPPV)

Zagreb, Croatia
1 year ago
Communication Skills
Medical Knowledge
Pharmacovigilance
Ergomed
Full-Time
Experienced

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