ro-774

Global Medical/Scientific Director / ro-774

Location
4001 Basel
Start
asap
End
30.09.2020
Workload
100 %
All-in / Hour
ask us for more details
Total Hours
1056
Deadline
Deadline
01.04.2020, 10am.
ro-774

Global Medical/Scientific Director / ro-774

Location
4001 Basel
Workload
100 %

Start DATE

asap

End Date

30.09.2020

DEADLINE

Deadline
01.04.2020, 10am.

  • 4001 Basel
  • Applications have closed
  • ro-7744001 Baselasap30.09.2020100 % 1056ask us for more detailsDeadline
    01.04.2020, 10am.

For our customer located in Basel/Switzerland we are currently looking for a: Global Medical/Scientific Director (m/f/d)

Background:

 

This position is a very operational role. Main responsibilities are oversight of PDMA clinical trials, as well as more traditional medical affairs activities including slide deck preparation, advisory boards and material development. There will be very little or no strategic aspect to this position and no line management responsibilities. Please do not send candidates with extensive leadership experience (or if you do, please make sure they fully understand the role is operational, not strategic). The contractor will be part of the Lung Cancer team alongside 10 other people all working on the same brand.

The ideal candidate is a rather junior (4/5 years – can be flexible on the number of years) with a Medical Degree or a PhD. The role will be on both MA responsibilities and PDMA sponsored trial oversight. This is why a Medical Doctor with experience in clinical science/medical monitoring and Medical Affairs experience is really ideal.

General Information

 

      • Start date: 16.03
      • Latest start date: April (1 month notice is highly preferred, 2 months is the maximum we can wait)
      • End date: 6 months
      • Extension: possible not guaranteed
      • Work location: Basel B1
      • Workload: 100%
      • Remote/Home Office: up to 1 day a week
      • Travelling: occasional
      • Team: 11 people (10 of them working on the same brand)
      • Department: PDMA Oncology, Lung & Rare Cancers

Tasks & Responsibilities

      • Oversee PDMA sponsored trials (that is why the MD degree is needed) which includes:
        -Medical and clinical oversight of assigned studies
        -Plan and exercise regular safety data review
        -Plan for study readout, interpretation and reporting of results
      • Contributes to establishing and implementing appropriate policies and standards for all activities of the medical plan for the therapeutic area (e.g. studies, publications, registries, KOL partnership).
      • Support the Lung Cancer team on slide decks, advisory boards, developing materials.

Must Haves

      • Minimum 4 years of experience in either Medical Affairs or Clinical Trial experience (clinical science/medical monitoring)
      • Degree in Life Sciences, preferably MD, but PhD with clinical trial experience will be considered
      • Experience with Oncology
      • Experience working in a global matrix environment
      • Team player, flexible and open to adapt to workload demand
      • Fluency in written and spoken English.

Nice to Haves

      • Experience with lung cancer and/or immunotherapy

Did we catch your interest?

The SymplyVision-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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