Medical Scientific Liaison

A global, continuously growing, pharmaceutical company is looking to appoint a Medical Scientific Liaison for their Nordic organisation. Selected candidate will be providing medical support to commercial teams on assigned products across Sweden (mainly Stockholm area).

Job Description

  • Status

    Position has been filled

  • Posted

    12 years ago

  • Employment Type

    • Permanent (Full-time)

  • Function

    • Medical Affairs

  • Industry

    • Pharmaceuticals

  • Therapeutic Areas

    • Immunology
    • Oncology

  • Seniority

    • Experienced

  • Location

    • Stockholm County, Sweden

  • Eligibility

    • EU/EEA/EFTA citizenship or a current permit to work and reside in Sweden.

  • Recruiter

Company Offers

  • An attractive compensation package with benefits (company car, health insurance, performance bonus, etc.);
  • A new challenge and prospects of career progression within a growing company;
  • A high level of responsibility and independence;
  • A supportive and friendly working environment.

Requirements

  • Life Science degree (ideally Medical);
  • At least 2 years previous experience in Medical Affairs within Pharmaceutical industry;
  • Familiar with study design, study evaluation, medical writing skills, expert panel conduct, symposium and workshop management, KOL management;
  • Good organizational skills with ability to work diligent, accurate and under pressure, alone or as part of a team;
  • Strong communication and presentation skills;
  • Fluency in English and Swedish, both written and spoken;
  • Computer literacy (Microsoft Office tools);
  • Ability to work in a cross-functional team (e.g., Marketing, Clinical Development, Regulatory, Drug Safety, etc.);
  • Prepared to travel locally and internationally.

Main Duties & Responsibilities

  • Developing and executing local medical strategies and medical activities for the products in accordance to internal and external regulations;
  • Providing medical support and trainings on assigned therapeutic area and/or product specifics;
  • Management of internal and external relationships within area of responsibility (e.g. KOLs);
  • Ensuring consistency of medical content and scientific messages across various tools and materials;
  • Involvement in the implementation of phase IV clinical development activities;
  • Regular reporting to the Nordic Medical Director.