Global Clinical Trials Intern — Data Analytics & Regulatory Support

MSD; Çankaya; Hybride; TRY 33 000 - 60 000; Temps partiel

Résumé du poste

MSD Türkiye offers an internship opportunity within Global Clinical Trials Operations (GCTO). Interns gain experience across Regulatory & Finance and Supply & CRA support, contributing to real-world projects and gaining hands-on exposure.

Responsibilities include assistance with submissions to regulatory authorities, safety document management, data mining, and dashboard analysis. The role is hybrid with potential travel and VISA sponsorship considerations.

Qualifications

• 4th year students or graduates from Science/Pharmacy Faculties.
• Good command of written and spoken English is preferred.
• Good command of MS Office applications.
• Self motivated with good communication skills.

Responsabilités

• Support Global Clinical Trials Operations Türkiye areas such as Regulatory & Finance and Supply & CRA support.
• Assist in preparation of submissions to regulatory authorities and management of safety documents.
• Contribute to data mining and dashboard analysis to support projects.
• Support post- monitoring visit preparations and document checks from Veeva.

Connaissances

Clinical Research

Data Analysis

Database Management

Detail-Oriented

Problem Solving

Project Management

Teamwork

Formation

Science/Pharmacy degree

Outils

MS Office

Veeva

Description du poste

MSD Türkiye offers an internship opportunity within Global Clinical Trials Operations (GCTO). Interns gain experience across Regulatory & Finance and Supply & CRA support, contributing to real-world projects and gaining hands-on exposure.

Responsibilities include assistance with submissions to regulatory authorities, safety document management, data mining, and dashboard analysis. The role is hybrid with potential travel and VISA sponsorship considerations.