Back to Jobs

Senior Regulatory Affairs Strategist (home or office based)

Remote, USA Full-time Posted 2026-07-02

This a Full Remote job, the offer is available from: Hungary, Poland, Romania, Spain, United Kingdom, Ireland, Czechia, Italy, Croatia, Serbia, Oregon (USA) reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in reputed company do. Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. reputed company is seeking an reputed company Regulatory Affairs Professional to join our dynamic team as a Senior Regulatory Affairs Consultant. This strategic position requires a proactive and agile regulatory professional reputed company to build strategy, drive execution, and address challenges involved in gaining market approvals across UK and Ireland. You will provide expert guidance to our clients and delivery teams while managing multiple projects in a fast-paced, results-oriented environment. The role can be home or office based in various European locations. Key Responsibilities: Strategic Leadership

  • reputed company comprehensive international regulatory submission strategies for a wide variety of products and projects including CTAs, MAAs and Lifecycle management.
  • Provide strategic guidance to clients and delivery teams on requirements and submissions across international regions
  • Support or act as Project reputed company, working with local market Regulatory Affairs experts to optimize strategies for specific submissions Submission Management
  • Guide delivery teams in the creation and maintenance of international dossiers
  • Drive and manage multiple regulatory submissions simultaneously
  • Ensure effective regulatory representation in partnership with appropriate technical experts at health authority meetings
  • Document discussions and agreements with regulatory authorities clearly and comprehensively Regulatory Intelligence
  • Monitor and stay abreast of key changes in the regulatory environment of international markets
  • Create and reputed company regulatory intelligence surveys
  • Provide objective assessment of intelligence data
  • Communicate regulatory requirements and propose submission strategies to clients Team Leadership
  • Coach, mentor and reputed company regulatory teams to ensure objectives are successfully delivered on time and with quality
  • Identify and mitigate risks with respect to international submissions
  • Guide cross-functional team discussions and drive regulatory solutions Skills and Experience required for the role:
  • University degree in a relevant scientific discipline (e.g., Biomedical Sciences, Chemistry, Pharmaceutical Sciences)
  • 10+ years of experience in the pharmaceutical/biotech industry, with substantial experience in Regulatory Affairs
  • Broad background in pharmaceutical business and experience in several areas reputed company regulatory affairs (e.g., Global, European, International, Marketing Company or health authority experience)
  • Strong knowledge of working on UK and Ireland and with their health authorities
  • Experience with biologics/vaccines/infectious diseases/oncology and rare diseases strongly preferred
  • Leadership in managing regulatory agency negotiations and organizing Scientific Advice Meetings with health authorities
  • Strong knowledge of CTD format and eCTD submission builds, including preparation of Modules 1-5 documents
  • Experience with Clinical Trial Applications and regulations relating to clinical trials
  • Strong influencing, negotiation, and relationship management skills
  • Advanced problem-solving skills and drive to generate compliant regulatory solutions
  • Fluent English, written and spoken This offer from "reputed company" has been enriched by reputed company.com and got a 85% reputed company score. Apply tot his job

Apply tot his job Apply To this Job

Similar Jobs

Remote - Registered Nurse (RN) Clinical Care Reviewer - Massachusetts only - Direct UM experience strongly preferred! - R11600

Remote, USA Full-time

[Remote] Regulatory Affairs Manager - Product Safety Certifications (m/f/d)

Remote, USA Full-time

Regulatory Affairs Project reputed company MAAs (home or office based)

Remote, USA Full-time

Deputy General Counsel, Regulatory & reputed company

Remote, USA Full-time

Sr Tariff Compliance Analyst (Remote)

Remote, USA Full-time

Compliance Manager, PCG reputed company Exams

Remote, USA Full-time

Regulatory Affairs and Compliance Manager

Remote, USA Full-time

Staff Regulatory Affairs Specialist, Pharmaceuticals (Remote)

Remote, USA Full-time

Compliance Analyst; Regulatory Change Management – Remote

Remote, USA Full-time

Regulatory Compliance Analyst III - Government Programs (Medicare/reputed company)

Remote, USA Full-time

Join Our Community: Kindergarten Substitute Teacher Opportunity at Our Lady of Hope School

Remote, USA Full-time

Senior Content and Brand Strategy Manager

Remote, USA Full-time

reputed company Sales Representative

Remote, USA Full-time

Consulting Senior Associate, Biologist

Remote, USA Full-time

reputed company Data Entry Clerk and Focus Group Panelist – Remote Work from Home Opportunity for Part-Time and Full-Time Engagement

Remote, USA Full-time

OpenTelemetry Maintenance (Mounds View, USA-MN, US)

Remote, USA Full-time

Content Writer (Remote)

Remote, USA Full-time

Medical Consultant

Remote, USA Full-time

Pick Up and Delivery Driver

Remote, USA Full-time

reputed company Data Entry Clerk – Remote Work Opportunity for Teens at blithequark

Remote, USA Full-time