EXPIRED – Director RWE & Innovative Evidence / no-392

Location
CH-Basel (St.Johann)
Start
01.06.2023
End
31.12.2023
Workload
100 %
All-in / Hour
see job description
Total Hours
1.216

Deadline:

Deadline
EXPIRED

 

EXPIRED – Director RWE & Innovative Evidence / no-392

Location
CH-Basel (St.Johann)
Workload
100 %

Start

01.06.2023

End

31.12.2023

DEADLINE

Deadline
EXPIRED

  • CH-Basel (St.Johann)
  • Applications have closed
  • CH-Basel (St.Johann)01.06.202331.12.2023100 % 1.216see job descriptionDeadline
    EXPIRED

For our customer located in Basel/Switzerland we are currently looking for a:  Director RWE & Innovative Evidence (m/f/d)

  • Location: CH-Basel (St.Johann)
  • Branch: Pharma
  • Duration: 01.06.2023 – 31.12.2023
  • Pay rate: (/1,34): 89 – 105 Chf/h

Tasks & Responsibilities

  • Develop and drive overarching innovative integrated evidence strategies, in col-laboration with internal partners, to ensure that the value of our medicines is fully supported by evidence.
  • Act as a thought-leader and internal change agent on matters pertaining to the overall creation and implementation of Innovative Medicines (IM) portfolio RWE / Integrated Evidence strategies and tactics.
  • Ask the right scientific questions, understand the evidence needs to optimize approval, access and clinical adoption of our medicines, and idea and make recommendations on fit-for-purpose data and integrated evidence solutions.
  • Deliver high quality, rigorous, and fit-for-purpose evidence solutions according to priorities and opportunities to impact patients and society.
  • Closely collaborate with internal and external partners ensuring scientific rigor in evidence strategy, study design and analyses.
  • Lead or contribute significantly to cross-functional, enterprise-wide and external evidence initiatives as well as to new and innovative data and analytic platforms, methodological approaches and technologies, which enable broader and more effective use of integrated evidence to reimagine medicine.
  • Work closely with key countries to develop timely, meaningful and robust evi-dence to support product value demonstration aligned with local needs (patient access, reimbursement, medical education, and patient advocacy).
  • Define and deliver on goals and objectives, identify opportunities, gaps and pri-orities, and contribute to best practice standards.

Must Haves

  • 7+ years industry and/or relevant experience acquired at biopharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies
  • Deep understanding and experience of RWD/RWE and/or related disciplines to generate scientifically rigorous and impactful evidence, both from prospective and retrospective studies, including secondary data sources.
  • Strong understanding of drug development with proven ability to identify and deliver impactful evidence from retrospective and prospective studies to optimize regulatory approval, market access and clinical adoption.
  • Strong cross-functional experience working with Clinical Development, Commercial, Market Access, HEOR, Medical, Safety, and Regulatory colleagues.
  • Deep understanding of and experience with research methodology and statistical methods related to retrospective and prospective clinical data analysis, and observational and/or epidemiological research.
  • Demonstrated track record leading and executing research projects using RWD from claims, electronic health records, registries, biobanks, or digital applications, including publications.

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

  • CH-Basel (St.Johann)
  • Applications have closed
  • CH-Basel (St.Johann)01.06.202331.12.2023100 % 1.216see job descriptionDeadline
    EXPIRED

For our customer located in Basel/Switzerland we are currently looking for a:  Director RWE & Innovative Evidence (m/f/d)

  • Location: CH-Basel (St.Johann)
  • Branch: Pharma
  • Duration: 01.06.2023 – 31.12.2023
  • Pay rate: (/1,34): 89 – 105 Chf/h

Tasks & Responsibilities

  • Develop and drive overarching innovative integrated evidence strategies, in col-laboration with internal partners, to ensure that the value of our medicines is fully supported by evidence.
  • Act as a thought-leader and internal change agent on matters pertaining to the overall creation and implementation of Innovative Medicines (IM) portfolio RWE / Integrated Evidence strategies and tactics.
  • Ask the right scientific questions, understand the evidence needs to optimize approval, access and clinical adoption of our medicines, and idea and make recommendations on fit-for-purpose data and integrated evidence solutions.
  • Deliver high quality, rigorous, and fit-for-purpose evidence solutions according to priorities and opportunities to impact patients and society.
  • Closely collaborate with internal and external partners ensuring scientific rigor in evidence strategy, study design and analyses.
  • Lead or contribute significantly to cross-functional, enterprise-wide and external evidence initiatives as well as to new and innovative data and analytic platforms, methodological approaches and technologies, which enable broader and more effective use of integrated evidence to reimagine medicine.
  • Work closely with key countries to develop timely, meaningful and robust evi-dence to support product value demonstration aligned with local needs (patient access, reimbursement, medical education, and patient advocacy).
  • Define and deliver on goals and objectives, identify opportunities, gaps and pri-orities, and contribute to best practice standards.

Must Haves

  • 7+ years industry and/or relevant experience acquired at biopharmaceutical companies, academia, healthcare provider / Payer / HTA, or relevant consultancy companies
  • Deep understanding and experience of RWD/RWE and/or related disciplines to generate scientifically rigorous and impactful evidence, both from prospective and retrospective studies, including secondary data sources.
  • Strong understanding of drug development with proven ability to identify and deliver impactful evidence from retrospective and prospective studies to optimize regulatory approval, market access and clinical adoption.
  • Strong cross-functional experience working with Clinical Development, Commercial, Market Access, HEOR, Medical, Safety, and Regulatory colleagues.
  • Deep understanding of and experience with research methodology and statistical methods related to retrospective and prospective clinical data analysis, and observational and/or epidemiological research.
  • Demonstrated track record leading and executing research projects using RWD from claims, electronic health records, registries, biobanks, or digital applications, including publications.

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

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