Paid Internship
Work Mode
Time Spent
Required Degree
Duration

Open Positions

Experience More On the Go

GET IT ONGoogle Play
Download on theApp Store
© 2026you'll get it. all rights reserved.

Internship Explorer

  • Explore
  • Saved Internships
Sign In

Internship Explorer

  • Explore
  • Saved Internships
Sign In
Paid Internship
Work Mode
Time Spent
Required Degree
Duration

22Open Positions

Auto-load
  • Intern Market Access

    Fondation Pierre Fabre
    Bruxelles, Belgium
    Found 1 week ago
  • Technical Writing Intern

    red-hat
    Brno, Czechia
    Found 1 week ago
  • Trainee Medical Writer - Internship

    CDM Barcelona
    Barcelona, Spain
    Found 3 weeks ago
  • Internship - Technical Writer

    Thermo Fisher Scientific
    Brno, Czechia
    Found 3 weeks ago
  • Assistant.e Medical Writer

    Havas Media France
    Puteaux, France
    Found 3 weeks ago
  • Werkstudent Projektmanagement Technische Redaktion Aftersales (w/m/x)

    BMW Group
    München, Germany
    Found 3 weeks ago
  • Technische Redaktion

    Workwise
    Berlin, Germany
    Found 4 weeks ago
  • Stage Redazione Tecnico-Tecnologico

    Mondadori Group
    Segrate, Italy
    Found 1 month ago
  • Werkstudent Technische Kommunikation (x|w|m) - Hybrid

    Sartorius
    Goettingen, Germany
    Found 1 month ago
  • Werkstudententätigkeit (m/w/d) Technical Communications

    Crown Gabelstapler GmbH & Co. KG - Deutschland
    Feldkirchen, Germany
    Found 1 month ago
  • Praktikant Technik- und Methodenkommunikation (w/m/x)

    BMW Group
    München, Germany
    Found 1 month ago
  • Student (m/w/d) Technische Redaktion

    NETZSCH Group
    Waldkraiburg, Germany
    Found 1 month ago
  • Praktikum/Abschlussarbeit - Benutzerdokumentation

    dSPACE
    Paderborn, Germany
    Found 1 month ago

Intern Market Access

Fondation Pierre Fabre
Found 1 week ago
Location
Bruxelles, Belgium
Time
Full-time
Work Mode
On-site
Salary
Not disclosed
Visa Help
Not disclosed
Last Verified
1 week ago

Education

  • Master

Skills & Qualifications

Technical Skills

  • Microsoft Office package (Excel ...)

Soft Skills

  • strong analytical
  • project management skills
  • detail-oriented
  • scientific value-based communication (medical writing)
  • understand and interpret clinical trials
  • enthusiastic
  • working towards providing patient access to innovative treatments
  • able to work independently
  • manage multiple projects
  • set priorities
  • meet deadlines

Job Description

Develop scientific knowledge of the therapeutic areas (oncology) Understand the Belgian, Netherlands and Luxembourg Healthcare system’s organizational structure and the decision-making process Create a based value communication / dossier writing (e.g. clinical evidence, local epidemiology, local guidelines etc,) to develop reimbursement submissions or revisions to meet country-specific market access needs and requirements in the BeNeLux region Support adaptation for regional market access and pricing materials (regional and global value dossiers, economic evaluations/Health Technology Assessment (HTA) e.g. cost-effectiveness analysis and budget impact models) for Pierre Fabre to develop reimbursement submissions and subsequent launches in the Benelux region Collaborate extensively with the medical and business teams and to support the reimbursement negotiation & processes Understand, follow and implement administrative and political mechanisms as well as the pricing regulations with internal key stakeholders for the Benelux Participate to various projects simultaneously across different therapeutic areas in conjunction with relevant Brand Teams

Requirements

  • Master of Science degree: PharmD, Epidemiology, Business engineering, Public Health, Pharmacy, Health Economics, Health Outcomes Research, Health Services Research, or other market access related program.
  • Interest in the Belgian or NE / Lux health care sector.
  • basic knowledge about HTA/economic evaluation in healthcare and pharmaceutical market access.
  • Experience in regulatory or regulatory affairs is an asset.
  • strong analytical and project management skills.
  • detail-oriented.
  • ability in scientific value-based communication (medical writing).
  • understand and interpret clinical trials (RCT’s) in terms of research design, methodology and results.
  • enthusiastic about working towards providing patient access to innovative treatments and carry out an attitude as such.
  • able to work independently, manage multiple projects, set priorities and meet deadlines.
  • master the Microsoft Office package (Excel ...).

Related Field

  • Product

Related Subfield

  • Product Management

Languages

  • Dutch
  • English
  • French

Nice to Haves

  • Experience in regulatory or regulatory affairs is an asset.
▶Apply Now

Similar Roles You Might Like

  • Clinical Study Administration - Student Placement

    Johnson & Johnson
    Leeds, United Kingdom
    Found 3 weeks ago
  • Research Assistant within Raman-based Therapeutic Drug Monitoring

    DTU - Technical University of Denmark
    Kgs. Lyngby, Denmark
    Found 1 month ago
  • Trainee - Market Analyst - Blood Market, Pharma Quality Control

    bioMérieux
    CRAPONNE, France
    Found 1 month ago
  • Clinical Trial Assistant 1 - Sponsor Dedicated- Prague

    IQVIA
    Prague, Czechia
    Found 2 months ago
  • Student Worker, Clinical Trial Delivery

    Genmab
    Copenhagen, Denmark
    Found 1 month ago
  • Intern GCO

    jd health
    Madrid, Spain
    Found 1 day ago