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SSU Regulatory Submissions Manager - Hybrid - Munich, Germany
122027
Posted:
26th
May 2023
- 60000 EUR - 60000 EUR
- Hybrid - Munich, Germany, Germany
- Permanent
** NEW OPPORTUNITY - Study Start Up Regulatory Manger - Global CRO - Hybrid - Munich, Germany **
Exceptionally excited to be able to announce that I am partnered with my mid-size global CRO client to support them in their search for an experienced SSU Regulatory Manager to join their growing team in Germany. A cornerstone hire for this business.
We are looking for a Senior SSU Regulatory Specialist with a solid backgroudn working within the Study Start Up/Regulatory Sector and who will have a strong understand of the Regulatory Submissions Lifecycle Process, who can aid to accelerate Clinical Trial Approval.
We are also looking for the candidate to have had some previous exposure to overseeing and managing the quality deliverables timeline for Regulatory Approval Process.
Our client holds a very unique space in the CRO market, which is unmatched elsewhere. They are a Global Organisation who have been established for over 30 years so bring resources, access to innovative studies and stability.
This is also a mid-size CRO which allows for them to take an extremely people centric approach, which cultivates flexibility, work/life balance and professional development and progression.
If you are in a post where you feel like your contributions go unnoticed or don't feel part of the success, this is absolutely the role for you.
I urge you to get in contact to discuss further.
Brendan Mulvaney
+44 203 019 3985
brendan.mulvaney@peoplewithchemistry.com
Exceptionally excited to be able to announce that I am partnered with my mid-size global CRO client to support them in their search for an experienced SSU Regulatory Manager to join their growing team in Germany. A cornerstone hire for this business.
We are looking for a Senior SSU Regulatory Specialist with a solid backgroudn working within the Study Start Up/Regulatory Sector and who will have a strong understand of the Regulatory Submissions Lifecycle Process, who can aid to accelerate Clinical Trial Approval.
We are also looking for the candidate to have had some previous exposure to overseeing and managing the quality deliverables timeline for Regulatory Approval Process.
Our client holds a very unique space in the CRO market, which is unmatched elsewhere. They are a Global Organisation who have been established for over 30 years so bring resources, access to innovative studies and stability.
This is also a mid-size CRO which allows for them to take an extremely people centric approach, which cultivates flexibility, work/life balance and professional development and progression.
If you are in a post where you feel like your contributions go unnoticed or don't feel part of the success, this is absolutely the role for you.
I urge you to get in contact to discuss further.
Brendan Mulvaney
+44 203 019 3985
brendan.mulvaney@peoplewithchemistry.com
Brendan Mulvaney
Lead Consultant