Gülşah Nomak
Medical Director at RS Research- Claim this Profile
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Bio
Credentials
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Introduction to the Principles and Practice of Clinical Research
The National Institutes of HealthJun, 2021- Nov, 2024 -
Biyoistatistik Okuryazarlığı
Akdeniz UniversityApr, 2021- Nov, 2024 -
BİGG+ Mentor Rozeti
Sum Koçluk Eğitim Danışmanlık A.ŞJan, 2021- Nov, 2024 -
Associate Certified Coach
ICF Turkey ChapterFeb, 2016- Nov, 2024 -
Business Development Mentor
House of Human Koçluk, Eğitim, DanışmanlıkJan, 2016- Nov, 2024
Experience
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RS Research
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Türkiye
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Biotechnology Research
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1 - 100 Employee
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Medical Director
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Jan 2022 - Present
- Medical strategy and clinical plan development- Medical input for drug development plan- Design and execution of clinical trial projects- Medical and clinical oversight for clinical trials.- Interaction with investigators, regulatory authorities, and KOLs.
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Board Member
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Dec 2021 - Present
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PDC Therapeutics
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Switzerland
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Research Services
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1 - 100 Employee
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Medical Director
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Jan 2022 - Present
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misPHARMA
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Türkiye
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Pharmaceutical Manufacturing
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Founder
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Aug 2019 - Present
Experienced Medical Affairs professional with a demonstrated history of working on several therapeutic areas in the pharmaceutical industry. Looking forward to utilize my experience to support medical teams by providing unique and influential content packages. Experienced Medical Affairs professional with a demonstrated history of working on several therapeutic areas in the pharmaceutical industry. Looking forward to utilize my experience to support medical teams by providing unique and influential content packages.
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Sanofi
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France
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Pharmaceutical Manufacturing
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700 & Above Employee
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Head of Medical Affairs - Diabetes & Cardiovascular
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Oct 2018 - Aug 2019
• Leading DCV Medical Team• Project team member for Standardization and Documentation of Congress / Meetings. • Leading DCV Medical Team• Project team member for Standardization and Documentation of Congress / Meetings.
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Bayer
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Chemical Manufacturing
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700 & Above Employee
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Medical Affairs Manager - Turkey, Iran, N. Africa & Patient Support Programs Responsible
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Jan 2016 - Oct 2018
• Leading Specialty Medcine Medical Team (11 FTE), 5 direct reports• Support Iran and North Africa countries as SM Medical Cluster Responsible, medical representative for TIM cluster in RCT meetings.• PSP Responsible for SM products and CRS Responsible for Mirena o Ensure operational excellence for all the Patient Support Programs by setting clear directions and ensure training of relevant staff. o Preparation of local PSDMP SOP o Patient Support Program Audit: No critical / major finding. o Team member in Global PSP CRM Project.• Medical affairs representative in Medical Device Regulations Project Group.• Project lead for Medical Affairs KPI Tracking Project.
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Group Medical Manager
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Dec 2010 - Dec 2015
• Responsible for Specialty Medicine and Radiology & Interventional products.• 11 direct reports (Medical Managers & MSLs)• PSP MA Contact for Specialty Medicine products.• Co-leading the regional (EMEA & LATAM) e-CME project.• Preparation of local NIS & ISS workflows to standardize the processes and ensure quality.• Leading “Brand excellence project”; preparation and implementation of a local guide.• Member of Non-Interventional Studies Protocol Review Committee.
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Project Manager
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Nov 2014 - Apr 2015
• Short-term assignment in Global Marketing Operations – Bayer AG• Project responsibility regarding Patient Support Programs; global framework had been prepared for PSP projects.
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Medical Manager
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Mar 2006 - Dec 2010
• Responsible for General Medicine products and Consumer Health products.• 1 direct report
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Education
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Istanbul University
Doctor of Philosophy - PhD, Clinical Research -
Acıbadem Üniversitesi
Master of Science (M.Sc.), Pharmaceutical Management -
Ege Üniversitesi
Bachelor of Science (BS), Faculty of Medicine -
Bornova Anadolu Lisesi (İzmir Koleji)
İngilizce