Job Description

Name of position: Intern

Location: Hybrid, Warsaw
Duration: 12 months

If you want to:

· Join a leading bio pharmaceutical company

· Gain hands-on experience in clinical research and Clinical Data Management

· Be part of a global team supporting high-quality clinical trial data

· Learn how end-to-end clinical trial data processes work in practice

Apply today!

Job overview:

As a Clinical Data Management Intern, you will support Clinical Data Managers in delivering high-quality clinical trial data. You will gain exposure to data governance, quality control, study metrics, and database lock preparation activities, while contributing to key Clinical Data Management processes in a global clinical trial environment.

What You’ll Do:

• Perform Sponsor Data Entry activities in line with study-specific guidelines and procedures

• Run and prepare data integrity and external data check reports

• Perform quality checks of scheduled data management deliverables

• Review selected clinical trial data and raise queries to investigational site staff, as applicable

• Support study milestone activities and database lock preparation

• Assist with study-level metrics and tracking activities

• Support additional end-to-end Clinical Data Management activities under the guidance of experienced Clinical Data Managers

You should apply if you have:

• B.A./B.S. degree or currently pursuing a Master's degree in a healthcare-related discipline (e.g., Biological Sciences, Pharmacy, Medicine, Pharmacy, Nursing)

• Fluent written and spoken English

• Good knowledge of Microsoft Office applications, especially Excel

• Strong attention to detail and commitment to data quality

• Good awareness of regulations and policies

• Ability to manage multiple tasks and work in a structured manner

We encourage you to apply, especially if you have:

• Interest in clinical research and clinical trial processes

• Curiosity and willingness to learn in a global team environment

• Analytical mindset and comfort working with data

• Motivation to contribute to the quality of clinical trial data

We set financial rates based on regular market reviews. We care about equality and comfort. We provide a high standard of work tools and great development opportunities.

Join us Today!

Required Skills:

Clinical Quality Assurance, Clinical Research, Database Management, Data Governance, Data Quality Control, Data Science, Data Visualization, Global Team Collaboration, Quality Assurance (QA), Quality Control Management

Preferred Skills:

Clinical Data, Data Integrity, Data Processing

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Intern/Co-op (Fixed Term)

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

not applicable

Job Posting End Date:

07/31/2026

*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.