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sheïma cankur, Premium Airports Services Agent

sheïma cankur

Premium Airports Services Agent·EMIRATES AIRLINES

United Arab Emirates

Master's degree, Drug Sciences, Aging and Anti-Aging Strategies

Work experience

Total years of experience: 4 years, 2 months

Premium Airports Services Agent

November 2025 - Present

EMIRATES AIRLINES

Dubai, United Arab Emirates

November 2025 - Present

Providing end-to-end operational support for First & Business Class and Economy passengers,
ensuring a seamless journey to our passengers through high-touch service and priority handling.
Autonomously managing technical delays, missed connections, and complex passenger re
protections in a fast-paced, high-stakes environment. Ensuring 100% adherence to global aviation
safety standards and internal Emirates protocols, maintaining meticulous documentation and data
integrity.
Company industry:
Airlines
Job role:
Hospitality and Tourism

Clinical Supply Chain Study Leader

September 2024 - September 2025

CAPGEMINI ENGINEERING

Montpellier, France

September 2024 - September 2025

«Lead of clinical supply chain of several clinical studies, including forecasting, stock management,
packaging and distribution plan/demands and IRT management
Integral supply set-up /supply follow-up / supply reconciliation of studies (internal or extemal)
Managed a full outsourced study and out licensed study
Core operational study meetings, regulatory compliance
Protocol. Pharmacy Manual and Instruction for Use contribution regarding Investigational Med
Products parts, Randomization lists creation (subjects, packaging and combined)
«Managed & authorized destructions on depots and investigational sites
Company industry:
IT Services
Job role:
Engineering

Clinical Supply Study Leader CAPGEMINI ENGINEERING for SANOFI

September 2024 - September 2025

SANOFI

Montpellier, France

September 2024 - September 2025

Lead of clinical supply chain of several clinical studies, including forecasting, stock management,
packaging and distribution plan/demands and IRT management / Integral supply set-up / supply
follow-up / supply reconciliation of studies (internal or external) / Managed a full outsourced study
and out licensed study / Core operational study meetings, regulatory compliance / Protocol,
Pharmacy Manual and Instruction for Use contribution regarding Investigational Medicinal Products
parts, Randomization lists creation (subjects, packaging and combined) / Managed & authorized
destructions on depots and investigational sites
Company industry:
Pharmaceutical Manufacturing

Clinical Supply Chain Project Manager Apprentice

September 2023 - September 2025

SANOFI

Montpellier, France

September 2023 - September 2025

«Improvement of Shipment Demand process (reduction of worldwide investigational products
distribution processs cycle time for investigational sites. improvement of dispensing rate)
«Conducted project risk analysis, developed blueprints, mapped processes. and presented
improvements to Leader Team.
Managed international project teams with daily English-language meetings
Optimization and management of shipments prioritization to improve logistics workflows and ensure
no patient missed visit in case of adverse events occurring during production. supply demand.
shipments or on-site storage (use of Power BI Dashboards)
Company industry:
Pharmaceutical Manufacturing

Clinical Supply Study Manager

September 2023 - August 2024

SANOFI Montpellier

Montpellier, France

September 2023 - August 2024

Process improvement engineering and clinical study supply / Clinical Supply Chain service
Optimization of the Shipment Demand Process Project: reflection, mapping and implementation of
the new process on Smartsupplies (PMD), Prioritization of shipment demands based on a Power BI
Dashboard and Participation and organization of meetings in English with French and international
teams
Company industry:
Pharmaceutical Manufacturing

Clinical Research Assistant - Promoter Department

September 2022 - February 2023

of Research and Innovation Montpellier Hospital

Montpellier, France

September 2022 - February 2023

Submissions of initial files to competent and regulatory authorities, substantial modifications,
monitoring of studies on site and remote, site initiations of studies, development and verification of
physical and investigative dematerialized workbooks
Company industry:
Medical Hospital

Clinical Research Associate Promoter Intern

January 2022 - January 2023

UNIVERSITY HOSPITAL OF LA COLOMBIERE

Montpellier, France

January 2022 - January 2023

« Ensured submission of clinical trials dossiers to regulatory authorities, substantial amendments
«Study monitoring (on-site and remote) and maintenance of investigator binders.
«Sites activations. development of studies set-up slideshows, archiving of paper studies & more.
Company industry:
Medical Hospital

Regulatory Affairs Manager Intern Direction of International Regulatory Affairs

January 2022 - January 2022

THT-BIO SCIENCES

Montpellier, France

January 2022 - January 2022

«Implementation of European Regulation 2017/7435 within the company, by setting up
manufacturer/distributor agreements
Export registration with export regulatory watch, assessment of local requirements
Redaction of procedures as part of the Quality Management System
Participation in a reference stop in gynecological surgery afier a loss of market
market. following refusal of intra-GSH listing by the Haute Autorité de Santé (French Health
Authority)
Company industry:
Medical & Healthcare Equipment

Clinical research associate intern

January 2021 - February 2021

CHU Lapeyronie Montpellier Professor PERS,

Montpellier, France

January 2021 - February 2021

Pre-screening, Inclusions visits with doctors, Patient following for studies on inflammatory
rheumatism, Patient data management
Company industry:
Medical Hospital
Job role:
Research and Development

Clinical Research Associate Intern in Investigation Rheumatology service

January 2021 - January 2021

UNIVERSITY HOSPITAL OF LAPEYRONIE

Montpellier, France

January 2021 - January 2021

Management and organization of clinical studies (phase I1. 111 and IV) on rheumatology
«Support to investigators (screening, inclusion and follow-up of patients)
• Assistance to clincal examinations
«Data management and processing (update of investigator file. date entry on electronical Case Report
Form. queries resolution)
Vigilance (reporting and follow-up of serious adverses events)
Archiving of documentation
Transporting biological samples to the operating rooms
Company industry:
Medical Hospital

Education

Faculty of Pharmacy

August 2024

August 2024

Master's degree, Drug Sciences, Aging and Anti-Aging Strategies

France

university

August 2024

August 2024

Master's degree, Aging and Anti-Aging Strategies Pharmacy

France

Pharmacy University

August 2022

August 2022

Master's degree, International Regulatory Affairs

France

University of Sciences Les Carmes

August 2021

August 2021

Bachelor's degree, Life Sciences

France

Université de Nîmes Les Carmes

June 2021

June 2021

Bachelor's degree, General Biology

France

Skills

COMPUTER LITERACY

Intermediate

CONCEPTUAL DESIGN

Intermediate

ENGINEERING ANALYSIS

Intermediate

FORECASTING

Intermediate

MANAGEMENT

Intermediate

OPERATIONS

Intermediate

PACKAGING AND LABELING

Intermediate

PHARMACY EXPERIENCE

Intermediate

RECONCILIATION

Intermediate

STOCK MANAGEMENT

Intermediate

COSMETIC DENTISTRY

Intermediate

COSMETICS

Intermediate

DRUG DEVELOPMENT

Intermediate

MARKETING

Intermediate

MEDICAL DEVICES

Intermediate

PHARMACEUTICALS

Intermediate

PHARMACOLOGY

Intermediate

PROJECT MANAGEMENT

Intermediate

PROJECT RISK MANAGEMENT

Intermediate

TOXICOLOGY

Intermediate

Languages

French

Beginner

English

Beginner

Spanish

Beginner

Trainings and Certifications

Certifications

Scientific Baccalaureate

Good Clinical Practices

Good Manufacturing Practices (GMP)

Hobbies and interests

travel
figure skating,
cinema,
Medicine,
travel
Cinema
Figure skating discipline
Team Work.