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Clinical Trial Trainee

Johnson & Johnson
Johnson & Johnson
Location: Prague, Czechia Posted on: 12 July 2026
CZ

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com . As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: R&D Operations Job Sub Function: Clinical Trial Support Job Category: Professional All Job Posting Locations: Prague, Czechia Job Description: Clinical Trial Trainee Duration: 12 months Location: Prague Join Johnson & Johnson as a Clinical Trial Trainee. This outstanding opportunity is open to final-year students or fresh graduates interested in working in the field of drug development. In this position, trainees will have the chance to learn various aspects of clinical trials, including regulatory rules, the basics of ICH GCP (Good Clinical Practice), gain basic therapeutic area knowledge and insights into the work of a Clinical Research Associate. Responsibilities of the Clinical Research Associate (CRA) that you will learn in this program include: Performing site identification, initiation, monitoring, and close-out visits. Providing administrative and logistic support to sites and the local team in supervising the trial's progress, handling study data and budget, organizing meetings, and other relevant tasks. Supervising study drug distribution and ensuring proper handling at the site. Collecting, reviewing, and tracking regulatory documents, site documentation, agreements, and training documentation. Evaluating the quality and integrity of documents and clinical trial site practices. What we offer in this trainee program: Part-time or full-time employment contract for one year. Broad experience in clinical research by shadowing an experienced CRA and gaining an overview of other positions in the clinical research department. Company computer, mobile, and employee benefits. Opportunity to acquire a position as a Clinical Research Associate after completing the program. Requirements: We are seeking fresh university graduates or students in their final year of university. Bachelor's or University degree in Life Science, Pharmacy, or Medicine. Proficiency in using Microsoft Word, Excel, and PowerPoint. Advanced English and Czech language skills. Excellent organizational and problem-solving abilities. Strong interpersonal skills. Ability to perform tasks accurately and in a timely manner. Required Skills: Preferred Skills: The anticipated pay range and benefits for this position is: 691050 CZK annually

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