EXPIRED – GMA Evidence Generation Operations Manager / ta-907

Location
CH-Zürich
Start
09.10.2023
End
09.10.2024
Workload
100 %
All-in / Hour
rate negotiable
Total Hours
2104

Deadline:

Deadline
EXPIRED

 

EXPIRED – GMA Evidence Generation Operations Manager / ta-907

Location
CH-Zürich
Workload
100 %

Start

09.10.2023

End

09.10.2024

DEADLINE

Deadline
EXPIRED

  • CH-Zürich
  • CH-Zürich09.10.202309.10.2024100 % 2104rate negotiableDeadline
    EXPIRED

For our customer located in Zurich/Switzerland we are currently looking for a: GMA Evidence Generation Operations Manager (m/f/d)

Manage assigned programs including Investigator Initiated Research (IIR), Externally Sponsored Collaborative Research (CCR), and Medical Affairs Company Sponsored Studies (MACS) within Plasma-dervied Therapy portfolio.

Tasks & Responsibilities

  • Oversee and manage studies and research portfolio, incl. review, initiation, tracking, closeout, and reporting of studies; coordinate finance and contract related aspects for globally funded research.
  • Responsible for the conduct of studies in accordance with all applicable internal legal and compliance policies (SOPs) as well as external local specific regulatory guidelines.
  • Serves as the operational area lead and process subject matter expert for interfacing with internal cross-functional global and local stakeholders and external investigators to develop and execute research plans and budgets
  • May be assigned to other tasks within the scope of Evidence Generation team including but not limited to, development of integrated evidence plans, process improvement initiatives, etc.

Must Haves

  • Minimum Master`s degree in a health or natural sciences related field
  • Minimum of 1 year of pharmaceutical, biotech or CRO industry experience
  • Ability to communicate and interact collaboratively and and appropriately with a variety of stakeholders both internal and external (i.e. senior directors, study investigators, vendors, CROs)
  • Ability to work independently in in a matrix, cross functional environment
  • Ability to manage tasks in multiple systems related to study management and oversight, finance, contracting, reporting, etc.

 

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.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Zürich
  • CH-Zürich09.10.202309.10.2024100 % 2104rate negotiableDeadline
    EXPIRED

For our customer located in Zurich/Switzerland we are currently looking for a: GMA Evidence Generation Operations Manager (m/f/d)

Manage assigned programs including Investigator Initiated Research (IIR), Externally Sponsored Collaborative Research (CCR), and Medical Affairs Company Sponsored Studies (MACS) within Plasma-dervied Therapy portfolio.

Tasks & Responsibilities

  • Oversee and manage studies and research portfolio, incl. review, initiation, tracking, closeout, and reporting of studies; coordinate finance and contract related aspects for globally funded research.
  • Responsible for the conduct of studies in accordance with all applicable internal legal and compliance policies (SOPs) as well as external local specific regulatory guidelines.
  • Serves as the operational area lead and process subject matter expert for interfacing with internal cross-functional global and local stakeholders and external investigators to develop and execute research plans and budgets
  • May be assigned to other tasks within the scope of Evidence Generation team including but not limited to, development of integrated evidence plans, process improvement initiatives, etc.

Must Haves

  • Minimum Master`s degree in a health or natural sciences related field
  • Minimum of 1 year of pharmaceutical, biotech or CRO industry experience
  • Ability to communicate and interact collaboratively and and appropriately with a variety of stakeholders both internal and external (i.e. senior directors, study investigators, vendors, CROs)
  • Ability to work independently in in a matrix, cross functional environment
  • Ability to manage tasks in multiple systems related to study management and oversight, finance, contracting, reporting, etc.

 

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.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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