Clinical Trials Operations Intern - Data & Regulatory Support

Merck; Çankaya; Hybrid; TRY 39,000 - 58,000; Part time

Benefits offered by this job

Hybrid work arrangement

Job summary

Merck Türkiye is offering an internship within Global Clinical Trials Operations. The role provides exposure to Regulatory & Finance and Supply & CRA support, with tasks spanning drug supply, payment management, and document checks using Veeva.

You will gain experience in clinical research, data analysis, and project coordination, collaborating with cross‑functional teams in a hybrid work setting. Preferred candidates are 4th‑year or graduate students from Science or Pharmacy faculties with

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.

Responsibilities

• Support regulatory submissions and data checks for trials.
• Assist in drug and non-drug supply management and payment/invoice tasks.
• Support safety document management and monitoring visit preparations.
• Contribute to data mining and dashboard analyses.

Skills

Clinical Research

Data Analysis

Database Management

Detail-Oriented

Problem Solving

Project Management

Teamwork

Education

Science or Pharmacy faculties (4th year student or graduate)

Tools

MS Office

Job description

Merck Türkiye is offering an internship within Global Clinical Trials Operations. The role provides exposure to Regulatory & Finance and Supply & CRA support, with tasks spanning drug supply, payment management, and document checks using Veeva.

You will gain experience in clinical research, data analysis, and project coordination, collaborating with cross‑functional teams in a hybrid work setting. Preferred candidates are 4th‑year or graduate students from Science or Pharmacy faculties with