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.