Global Medical Director / Global Scientific Director (m/f/d)

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Beschreibung



Global Medical Director / Global Scientific Director (m/f/d)

Reference: -en
Start: asap
Duration: 12 MM++

Main tasks:
  • Responsible for the execution of the Medical Strategy for the assigned product(s) / Indication(s)
  • For some projects you may be accountable for the evidence generation strategy planning and/or execution, incl. (but not limited to) identifying medical and access gaps and needs as part of the overall medical strategy 
  • Accountable for evidence generation activities for the assigned product (s) / Indication(s), including risk benefit assessment and medical monitoring in all medical affairs interventional studies
  • Take the role of Lead Scientific Responsible and acts as a member of the Study
  • Conduct review and approval of investigator initiated studies (IIS) and supported study proposals (incl. Review of affiliate study synopses and sign off of affiliate studies)
  • As appropriate, provide medical expertise and scientific data to support Regulatory, Drug Safety, Health Economics and Public Policy strategy and documents  
  • Assess the needs and coordinates compassionate use of the assigned product(s)
  • Review and make clinical assessment of compassionate use of the assigned product(s)
  • In collaboration with Global Access (GA) and appropriate Affiliates stakeholders, identifiy the evidence generation needs/gaps in order to obtain and maintain patient access and integrates them into the evidence generation strategy
  • Provide medical expertise and input into the market access, brand and lifecycle strategies and plans (e.g. Life Cycle Plans, Brand Plans, Launch Plans, Comparative Benefit Risk Assessments and other relevant documents
  • As appropriate, represent and provide medical expertise to the appropriate Global Access teams and other relevant teams
  • For some projects, you may drive and lead the strategy of the integrated evidence generation activities, incl. sponsored clinical studies, Investigator Initiated Studies (IIS), RWD
  • Develop, advance and maintain TAE interactions and collaborations, incl. those aimed to set up and conduct evidence generation activities
  • Represents the company in peer-to-peer interactions with external collaboration partners, including in patient-company interactions
  • Responsible for acting in line with legal, regulatory and company standards and codes of practice 


Main qualifications
  • Profound experience in Medical Affairs in pharma (global or regional) 
  • Medical Doctor or PhD in Life Sciences with relevant clinical experience 
  • Previous experience working in Compassionate Use Program / patient care in clinical trials (experience with 1st patient is ideal) with decision making on treatment
  • Experience in Hematology / Lymphoma


Main advantages:
  • A highly motivated team and an open way of communication
  • Dynamic and innovative market environment
  • Good infrastructure
  • You will work in an international environment



About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays:

My contact person:
Marija Tomas

Referencenumber:


Make contact:
Email:
Start
ab sofort
Dauer
12 MM++
(Verlängerung möglich)
Von
Hays AG
Eingestellt
16.06.2020
Ansprechpartner:
Kerstin Werner
Projekt-ID:
1936947
Vertragsart
Freiberuflich
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