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    Integrated Data Analytics and Reporting (IDAR) Training Associates - (Multiple Functions)  

    At Johnson & Johnson, we use technology and the power of teamwork to discover new ways to prevent and overcome the world’s the most significant healthcare challenges. Our Corporate, Consumer Health, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make life-changing healthcare products and medicines. We're disrupting outdated healthcare ecosystems and infusing them with transformative ideas to help people thrive throughout every stage of their lives. With a reach of more than a billion people every day, there’s no limit to the impact you can make here. Are you ready to reimagine healthcare? 

    Here, your career breakthroughs will change the future of health, in all the best ways. And you’ll change, too. You’ll be inspired, and you’ll inspire people across the world to change how they care for themselves and those they love. Amplify your impact. Join us! 

    Janssen Research and Development, L.L.C., a member of the Johnson and Johnson Family of Companies, is recruiting University Graduates (undergraduate and post-graduate) for our Integrated Data Analytics and Reporting (IDAR) Training Academy! The Janssen Integrated Data Analytics and Reporting organization includes the following Departments: Clinical and Statistical Programming (C&SP), Data Management (DM), Risk Management and Central Monitoring (RM-CM), and Regulatory Medical Writing (RMW).   

    We are seeking highly motivated candidates to join our IDAR Academy. The Academy is a premier training program focused on developing and inspiring talents to become full time members of our teams. You can help advance our medicines in development at Janssen! Remote work options may be considered on a case-by-case basis and if approved by the Company.  

    Please indicate department of your primary interest from the following (note: final placement in a department will be determined after all candidates have been selected): 

    • C&SP provides analytical programming solutions that enable early and effective decisions.  The role within C&SP plans, designs, and develops codes to support clinical data review, visualizations, analysis and reporting activities.  C&SP collaborates with biostatistics and other functions to achieve project goals.  How you can make a difference:  Apply your knowledge of data structures and programming languages (eg, SAS, R, and Phyton) to the analysis and reporting of our clinical trial data.  

    • DM provides data delivery expertise in the conduct of our clinical trials. The aim is to develop a database to capture data, oversee data cleaning activities and deliver data that meets the standards for potential submission to regulatory authorities. In this role you will interact with different cross-functional team members and external partners. How you can make a difference: Apply your strong task prioritization, organization, problem solving skills, and attention to detail to the collection and cleaning of our clinical trial data.  

    • RM-CM leads the risk-based approach to monitoring clinical trials to help ensure protection of human subjects and the quality of clinical trial data. The RM-CM group is responsible for each detection, analysis, and mitigation of potential risks in clinical trials.  How you can make a difference:  Apply your knowledge of data science, analytical acuity, understanding of statistical concepts, and ability to learn and adapt to new technology to the monitoring of our clinical trials.  

    • RMW writes high quality clinical documents to support the development, regulatory approval, and maintenance of our products.  These documents include investigator’s brochures, clinical protocols, clinical study reports, summaries of efficacy and safety from clinical trials, and responses to questions from health authorities.  How you can make a difference:  Apply your excellent writing skills, ability to interpret and summarize statistical and medical information, and attention to detail to the design of our clinical trials and reporting of our data.  


    Qualifications

    Education Requirements:  

    Bachelor’s degree and/or equivalent is required. An advanced degree is preferred. 

    Education Preferences:  

    C&SP 

    Preferred fields of study are computer science, data science/data engineering, mathematics, or another relevant scientific field. 

    DM 

    Preferred fields of study are health sciences or another relevant scientific field.  

    RM-CM 

    Preferred fields of study are data science, engineering, computer science, and/or other health-related or scientific fields.  

    RMW 

    Preferred fields of study are biological science, pharmacy, pharmacological science, or another health-related scientific or medical field.

    Are you ready to impact the world? 

    For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.  

    We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we in EMEA are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential.  

    No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”! 

    Please note that we plan to close for first round of applications on 30th October, but could close earlier if we receive too many applications