Clinical Research Intern

3328 MSD Ilaclari Ltd STI; Çankaya; Hybrid; TRY 33,000 - 60,000; Part time

Job summary

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.

Responsibilities

• 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.

Skills

Clinical Research

Data Analysis

Database Management

Detail-Oriented

Problem Solving

Project Management

Teamwork

Education

Science/Pharmacy degree

Tools

MS Office

Veeva

Job description

Job Description As Global Clinical Trials Operations (GCTO) Türkiye, we provide our interns the opportunity to work on meaningful assignments and make sure that they gain real world experiences (in the areas of Regulatory & Finance and Supply & CRA support) As an intern, you may provide support to these areas; examples include; Drug & Non Drug Supply Management Payment and Invoice Management Document & report checks from Veeva Preparation of submissions to regulatory authorities Management of safety documents Pre and Post Monitoring Visit Preparations Data Mining and Analysis in dashboards

• Drug & Non Drug Supply Management
• Payment and Invoice Management
• Document & report checks from Veeva
• Preparation of submissions to regulatory authorities
• Management of safety documents
• Pre and Post Monitoring Visit Preparations
• Data Mining and Analysis in dashboards

Qualifications

• 4th years 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

Required Skills

• Clinical Research
• Data Analysis
• Database Management
• Detail-Oriented
• Problem Solving
• Project Management
• Teamwork

Employee Status: Intern/Co-op (Fixed Term)

Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s):

Job Posting End Date: 11/9/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.