LOUIS LEO MUGITA

London,United Kingdom

Summary

Experienced medical writer with 5 years in pharma advertising and medical communications. Skilled in creating HCP and patient materials across Over-the-Counter and Prescription-Only Medications. Well-versed in ABPI, PAGB, and ICH guidelines, with a strong portfolio spanning both commercial and medical communication sectors. Known for delivering compliant, clear, and effective content that supports organisational goals.

Overview

years of professional experience

year of post-secondary education

Work history

LEAD MEDICAL WRITER (HEALTHCARE AND PHARMA)

KINESSO (UK and IRELAND) – IPG MEDIABRANDS

02.2023 - 07.2025

Leading creation and review of promotional and non-promotional material within Code-stipulated guidelines.
Serving as content manager for Kenvue accounts, including Sudafed, Acuvue, Listerine, and Benylin.
Managing client account performance and spending through content audits and strategic content planning.
Creating commercial and patient awareness materials in line with a drug's SmPCs and market authorisation.
Formulating and executing content plans for both medical communications projects and commercial, consumer-facing (OTC) projects.
Collaborating with Design, PR, and SEO teams to deliver within budget allocations and project timelines.
Mentoring junior writers and leading internal workshops on ABPI and MHRA guidelines.
Maintaining professional integrity in client and HCP relationships by addressing client inquiries and concerns appropriately.
Applying my experience across different therapy areas, such as oncology and cardiology.
Ensuring an AMA-style approach and ABPI Code compliance across various communications and commercial materials, including HCP newsletters, congress materials, and online website materials.
Ensuring Veeva content and claims compliance are accurate to streamline clients’ internal approval process.
Engaging digital audiences with fresh, modern copy for static and interactive pages.
Liaising effectively with subject matter experts to validate the accuracy of scientific content.
Developing brochures and posters for healthcare campaigns, contributing towards successful outreach efforts.
Creating engaging content for healthcare websites, resulting in higher user engagement.
Enhancing understanding of medical literature by conducting thorough and detailed research.
Prepare mock medical content for B2B (C-suite) pitches and presentations

MEDICAL WRITER

The National Leadership Academies (USA)

11.2020 - 01.2023

Company Overview: National Academy for Future Physicans and Medical Scientists
Simplifying Phase III trial data for educational publications.
Developing career pathway programs for aspiring medical students.
Reporting on oncology and longevity seminars with emphasis on breakthrough trends.
Reviewing content per AMA Manual of Style standards.
Receiving Medical Affairs training with a strong understanding of Clinical guidelines (ICH).

Education

ABPI Code of Practice - Advanced Medical Representative Programme - CVD & Oncology Specialty

Association of British Pharmaceutical Industry

08.2024 - 02.2025

Bachelor of Science - Electrical Engineering

Dedan Kimathi University

Skills

Regulatory compliance
Medical/Technical Writing
Content performance Auditing
Client engagement and strategy
Medical communications

Phase III & IV (post-market surveillance) interpretation and analysis
ABPI Code of Practice
PAGB Professional and Consumer Codes
ICH guidelines
Pharmacovigilance

FUTURE ASPIRATIONS

Looking to pursue the RAC Drugs exam to strengthen my regulatory affairs expertise and become a key asset in drug submissions.
RAPS validates knowledge in global pharmaceutical regulations, clinical trials, and drug development.
This ensures I can navigate complex regulatory landscapes with confidence and compliance.

Languages

English

Proficient (C2)

Swahili

Advanced (C1)

Timeline