Associate-Director Global Medical Affairs

Associate-Director Global Medical Affairs

Sobi

Basel, Switzerland

Role & Function

The Global Medical Affairs Associate-Director will contribute to the development of medical strategy, planning & execution of medical affairs activities with the benefit of the patient at the forefront and ensures medical activities are delivered with integrity and scientific accuracy. He/she will provide scientific and medical leadership by thoroughly understanding the product and relevant disease areas, and serving as a scientific and medical resource.

The Global Medical Affairs Associate-Director works within a matrix organization, a multi-functional Global Medical Product Team with a focus on deliverables supporting the strategic and tactical plans. (medical/clinical operations, scientific communications, medical affairs). The Global Medical Affairs Associate-Director also represent Sobi towards external collaborators such as health care practitioners, medical associations, research groups.

Key Responsibilities

  • Apply therapeutic/disease area expertise and clear business understanding to address current and future medical needs in clinical practice with medically appropriate use of investigational medicines;
  • Provide hands on support in management, generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high quality publications;
  • In a matrix, medical project team, continuously strives for alignment across the organization (and the alliance if applicable) and ensure delivery of all medical objectives, to agreed timelines, cost and quality;
  • Contribute to internal medical launch readiness;
  • Establish and maintain Sobi as a scientific partner in clinical community, innovating in stakeholder engagement plan for the specific therapy areas;
  • Ensure internal high standard medical knowledge in specific therapy area;
  • Ensure adherence to safety and regulatory requirements for the assigned product;
  • Ensure that all medical deliverables are compliant with internal SOPs as well as international compliance guidelines and regulatory requirements.

Personal attributes

  • Demonstrated leadership skills including e.g. build, lead and motivate workstreams/projects;
  • Ability to see a complex program from a "big picture"/strategic level;
  • Strong interpersonal skills with communicative and flexible attitude;
  • Excellent written and oral communication skills;
  • Good influencing skills and Interpersonal skills;
  • Excellent problem-solving skills, results and action oriented, hands-on;
  • Performs competently in a multicultural environment.

Qualifications

  • Life science degree MD or PhD with a minimum of 4 years’ experience within pharmaceutical industry (local, regional, global);
  • Experience with medical affairs launch strategy development, and execution;
  • Experience in clinical research process, conception and execution of clinical trials, (and phase IV, RWE); knowledge of clinical trial design, statistics, and data analysis; able to lead interpretation of data and impact on medical strategy;
  • Demonstrated outstanding external medical experts and community engagement;
  • Good understanding of Patient Access strategy and overall business priorities;
  • Excellent project management skills including risk assessment and contingency planning;
  • Demonstrated skills in functioning in global, matrix, multi-disciplinary teams.

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© EuroJobsites 2021

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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