Experience

DeSia Clinical Research

• Türkiye
• Research Services
• 1 - 100 Employee

• Medical Writer

  • Oct 2022 - Present



GAMA CRO Contract Research Organization Trade Limited Company

• Türkiye
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Bioequivalence Director at Gama CRO

  • Jun 2021 - Aug 2021



MEDEX SMO

• Türkiye
• Medical Practices
• 100 - 200 Employee

• Bioequivalence Specialist Pharmacokineticist and Biostatistician

  • Nov 2020 - Jun 2021

  - Experience in producing detailed Bio-equivalence study protocols, Consent forms and Case Report Forms (CRF). - Experience in performing the pharmacokinetics calculations using Winnonlin software. - performing Statistical calculations using SAS software to check for (Descriptive Analysis, Normality test, Levene Test for Homogeneity, Outlier Analysis, ANOVA, Schuirmann two one sided test, Confidence Interval Analysis, Sample Size and Power determination). - Responsible of processes including maintaining, receiving, labeling and dispensing of the test and reference pharmaceutical products in the pharmacy according to regulations. - Data entry and issuing of clinical, pharmacokinetics and statistical reports after finalizing the study periods. - Attending Institutional Review Board (IRB) Meetings. - ICH GCP, GCDMP regulations. Show less



International Center for Bio-availability, Pharmaceutical, and Clinical Research (ICBR)

• Egypt
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Data Management Specialist

  • Feb 2017 - Nov 2020

  - Experience in producing detailed Bio-equivalence study protocols, Consent forms and Case Report Forms (CRF). - Experience in performing the pharmacokinetics calculations using Winnonlin software. - performing Statistical calculations using SAS software to check for (Descriptive Analysis, Normality test, Levene Test for Homogeneity, Outlier Analysis, ANOVA, Schuirmann two one sided test, Confidence Interval Analysis, Sample Size and Power determination). - Responsible of processes including maintaining, receiving, labeling and dispensing of the test and reference pharmaceutical products in the pharmacy according to regulations. - Data entry and issuing of clinical, pharmacokinetics and statistical reports after finalizing the study periods. - Attending Institutional Review Board (IRB) Meetings. - ICH GCP, GCDMP regulations. Show less



Eimc united Pharmaceuticals

• Badr City

• QC Analyst

  • Mar 2011 - Sep 2012



GSK

• United Kingdom
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Medical Representative

  • Jan 2010 - Dec 2010