Medical Director (m/w/d) at LEO PHARMA AS
63263 Neu-Isenburg, , Germany -
Full Time


Start Date

Immediate

Expiry Date

26 May, 25

Salary

0.0

Posted On

25 Apr, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research, Pharmaceutical Industry, Dermatology, International Travel, Biologics, Communication Skills, Market Access, Launch Experience, Stakeholder Management, Strategy, Medical Communications, Drug Development

Industry

Pharmaceuticals

Description

Tätigkeitsbereich: Regulatory & Medical
Veröffentlichungsdatum: 24.01.2025
Arbeitsort: Neu-Isenburg 63263, Hessen, hybrides Arbeitsmodell
Vertragsart: unbefristete Festanstellung in Vollzeit
Stelle ID: 2884

EXPERIENCE

  • MD Degree preferred and experience within a similar role
  • Minimum of 10 years demonstrable experience, within the pharmaceutical industry, in medical affairs and or in clinical research and development
  • Solid knowledge of drug development, safety, regulatory, market access and reimbursement requirements
  • Experience in dermatology preferred as well as launch experience
  • Experience working with biologics preferred

COMPETENCIES & SKILLS

  • Excellent leadership and communication skills, with the ability to build strong relationships at all levels of the organization
  • Fantastic stakeholder management both internally and externally
  • Ability to translate strategy to execution and drive the organization forward in executing and delivering results.
  • Highly accountable with the ability to lead, drive and embed change both technically and behaviourally
  • Strong business and commercial acumen with the ability to influence and also identify cost efficiencies
  • Track record of cross-functional collaboration (preferably with commercial, legal, regulatory, and medical communications)
  • Strong goal orientation, an ability to make decisions and a history of meeting deadlines and objectives
  • Strong English verbal and written communication skills
  • Experience in developing and expanding key external expert relationships
  • Skilled in developing, reviewing, understanding, and presenting clinical and scientific information to multiple audiences
  • Creates and enhances a culture of compliance, integrity, pro-activeness, and collaboration Willing and able to undertake significant domestic and international travel (could be as much as 20-30%).
Responsibilities

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