Intern

Job description

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.