Senior Medical Affairs Manager

i-Pharm Consulting; Greater London; On-site; GBP 60,000 - 100,000; Full time

Job summary

Ein führendes multinationales Biopharmaunternehmen sucht einen Senior Manager für medizinische Angelegenheiten mit Schwerpunkt auf der Generierung von Real-World Evidence (RWE). In dieser strategischen Rolle werden Sie die Planung und Durchführung von Beobachtungsforschungsstudien unterstützen, die die Zukunft des Gesundheitswesens gestalten. Sie bringen wissenschaftliche Strenge und strategische Einsichten in jedes Projekt ein, von der Studiengestaltung bis zur Einbindung von Interessengruppen. Diese Position bietet die Möglichkeit, in einem globalen, innovativen Umfeld zu arbeiten und Ihre Karriere in der medizinischen Forschung voranzutreiben.

Qualifications

• Erfahrung in RWE, Beobachtungsforschung oder Gesundheitsökonomie.
• Starke Kommunikations- und Studienmanagementfähigkeiten erforderlich.

Responsibilities

• Entwerfen und Ausführen von Studien zur Krankheitslast und Prävalenz.
• Unterstützen von RWE-Plänen für Regulierungsbehörden und Kliniker.

Skills

Kommunikationsfähigkeiten

Studienmanagement

Epidemiologie

Biostatistik

Gesundheitsökonomie

Education

MSc in einem wissenschaftlichen Bereich

PharmD

PhD

MD

Tools

R

SAS

SPSS

Stata

Job description

2 days ago Be among the first 25 applicants

Get AI-powered advice on this job and more exclusive features.

Direct message the job poster from i-Pharm Consulting

Providing expert temporary talent solutions for the life sciences industry, with a specialised focus on Quality Assurance and Technical Operations

Senior Manager, Medical Affairs – Real-World Evidence Generation

We're hiring on behalf of a leading multinational biopharmaceutical client for a Senior Manager in Medical Affairs, focused on Real-World Evidence (RWE) Generation. If you’re an experienced professional in medical affairs or observational research and ready to step into a strategic, cross-functional role—this is your opportunity to make an impact.

The Role

You’ll support the planning and delivery of observational research studies that help shape the future of healthcare. From study design to stakeholder engagement, you’ll bring scientific rigour and strategic insight to every project.

What You’ll Be Doing

1. Design and execute studies on disease burden, prevalence, and natural history
2. Support real-world evidence plans for regulators, payers, and clinicians
3. Develop historical control methods and performance metrics
4. Write and review study protocols, SAPs, and clinical reports
5. Collaborate with internal and external experts, regulators, and advocacy groups
6. Provide scientific input for regulatory filings and responses

What We’re Looking For

1. MSc, PharmD, PhD or MD in a scientific field (epidemiology, biostatistics, health outcomes etc.)
2. Experience in RWE, observational research, or health economics
3. Strong communication and study management skills
4. Knowledge of statistical tools like R, SAS, SPSS, or Stata

Bonus if you have:

1. Background in oncology or haematology
2. Experience in regulatory interactions and evidence generation strategy

Why Apply?

1. Join a global, innovative environment tackling real-world health challenges
2. Work alongside top-tier professionals across medical, clinical, and commercial teams
3. Grow your leadership profile and expand your career in medical affairs and RWE

Ready for your next step? Apply now and bring your expertise to where it matters.

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Science and Quality Assurance

Industries

Pharmaceutical Manufacturing and Biotechnology Research