Ayşe Göklü Şenol

Ayşe Göklü Şenol Email and Phone Number

Regulatory Affairs & Business Development Manager @ VEM İLAÇ SAN. TİC. A.Ş.
Ayşe Göklü Şenol's Location
Ankara, Türkiye, Turkey
About Ayşe Göklü Şenol

Ayşe Göklü Şenol is a Regulatory Affairs & Business Development Manager at VEM İLAÇ SAN. TİC. A.Ş.. They possess expertise in pharmaceutical industry, project management, gmp, biotechnology, clinical trials and 9 more skills.

Ayşe Göklü Şenol's Current Company Details
VEM İLAÇ SAN. TİC. A.Ş.

Vem İlaç San. Ti̇c. A.Ş.

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Regulatory Affairs & Business Development Manager
Ayşe Göklü Şenol Work Experience Details
  • Vem İlaç San. Ti̇c. A.Ş.
    Regulatory Affairs & Business Development Manager
    Vem İlaç San. Ti̇c. A.Ş. Feb 2021 - Present
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  • Vem İlaç San. Ti̇c. A.Ş.
    Regulatory Affairs Manager (Alternate) & Business Development Executive
    Vem İlaç San. Ti̇c. A.Ş. Mar 2020 - Present
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  • Vem İlaç San. Ti̇c. A.Ş.
    Business Development Executive & Senior Regulatory Affairs Specialist
    Vem İlaç San. Ti̇c. A.Ş. Oct 2011 - Mar 2020
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  • Bio-Gen Pharmaceuticals
    Regulatory Affairs Specialist
    Bio-Gen Pharmaceuticals May 2009 - 2010

Ayşe Göklü Şenol Skills

Pharmaceutical Industry Project Management Gmp Biotechnology Clinical Trials Market Access Regulatory Affairs Pharmaceutics Regulatory Requirements Regulatory Submissions Science Validation Ectd Oncology

Ayşe Göklü Şenol Education Details

Frequently Asked Questions about Ayşe Göklü Şenol

What company does Ayşe Göklü Şenol work for?

Ayşe Göklü Şenol works for Vem İlaç San. Ti̇c. A.ş.

What is Ayşe Göklü Şenol's role at the current company?

Ayşe Göklü Şenol's current role is Regulatory Affairs & Business Development Manager.

What schools did Ayşe Göklü Şenol attend?

Ayşe Göklü Şenol attended Hacettepe Üniversitesi, Hacettepe Üniversitesi, Hacettepe Üniversitesi.

What skills is Ayşe Göklü Şenol known for?

Ayşe Göklü Şenol has skills like Pharmaceutical Industry, Project Management, Gmp, Biotechnology, Clinical Trials, Market Access, Regulatory Affairs, Pharmaceutics, Regulatory Requirements, Regulatory Submissions, Science, Validation.

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