Medical Manager, Baltics

A global pharmaceutical company is looking to appoint a Medical Manager for the Baltic States, who will be responsible for the development and execution of medical plans to support the strategic and operational goals of the business.

Job Description

  • Status

    Position has been filled

  • Posted

    10 years ago

  • Employment Type

    • Permanent (Full-time)

  • Function

    • Medical Affairs

  • Industry

    • Pharmaceuticals

  • Seniority

    • Manager

  • Location

    • Tallinn, Estonia

  • Eligibility

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

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

Requirements

  • Life Science education (ideally Medical Doctor or postgraduate in Pharmacy, Microbiology, Molecular Biology, etc.);
  • At least 3-4 years direct Medical Affairs experience within pharmaceutical industry (review of promotional materials, medical education, medical writing, study design, study evaluation, expert panel conduct, symposium and workshop management, KOL management, etc.);
  • Experience in an operational management and/or leadership role;
  • Experience with Biological products would be desirable and advantageous;
  • Strong existing professional relationships with Key Opinion Leaders;
  • Excellent communication and presentation skills;
  • Fluency in English and Lithuanian or Estonian, both written and spoken. Ability to at least speak and read in Russian;
  • Computer literacy (Microsoft Office tools);
  • Prepared to travel locally and internationally (up to 20-30% of the time).

Main Duties & Responsibilities

  • Develop and implement medical strategies to achieve maximum competitive advantage for company's products;
  • Provide leadership in developing and maintaining professional relationships with scientific community (physicians, key opinion leaders, scientific societies, etc.), policy makers and other relevant stakeholders;
  • Provide medical and scientific expertise in variety of therapeutic areas;
  • Coordinate advisory boards, expert and scientific meetings;
  • Ensure accuracy of medical content and scientific messages across various tools and materials;
  • Gather competitive intelligence and maintain in-depth knowledge;
  • Oversee regulatory and safety activities for the assigned portfolio of products (PSURs, ARs, label harmonisation, etc.);
  • Oversee training and development of the medical team (3 direct reports) to meet business needs and deliver quality services;
  • Report directly to the regional Medical Director.