DirecciónAt Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose : to transform the history of health in humanity.
Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years.
Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.
When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough. At Janssen, we're creating a future where disease is a thing of the past.
We're the Pharmaceutical Companies of Johnson & Johnson, working tirelessly to make that future a reality for patients everywhere by fighting sickness with science, improving access with ingenuity, and healing hopelessness with heart.
We focus on areas of medicine where we can make the biggest difference : Cardiovascular & Metabolism, Immunology, Infectious Diseases & Vaccines, Neuroscience, Oncology, and Pulmonary Hypertension.
We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it.
Please visit https : / / www.janssen.com / for more information. We are searching the best talent for Regulatory Affairs Analyst (Cross Country) to be in Latin America-Argentina-Buenos Aires / Other locations : Latin America, other countries (Mexico, Brazil, Chile, Colombia, etc).
Purpose : Data Entry Specialist, supporting and contributing in the deployment of the RA systems use across the LATAM región.
You will be responsible for :
- Ensure flawless implementation of the data management center.
- Ensure data entry into the regulatory systems (LIFT, ERIS, Insight, WebTcards, RIM docs & SPS).
- Guarantee accuracy and quality of the data process into the systems.
- Secure systems compliance in all the clusters across the region.
- Identify opportunities for improving how the data is manage.
- Become expert of the regulatory systems.
- With the knowledge of the system and the business processes, contribute to robust SOPs, WIs and job-aids.
- Provide support and training to the RCMs / LOCs for accessibility of the RA system and tools.
- Close collaboration and communication with LOCs, regional and global stakeholders.Qualifications and requirements :
- University degree or equivalent by experience.
- Has applicable experience in Regulatory Affairs.
- Is familiar with relevant business processes and systems.
- Has an affinity for IT-systems and has fluent communication skills in English
- Key interactions : LA RMC, LoCs, LARO, Systems Global team.
- System interactions : WebTcards, Insight, LIFT, RIM docs.
- KPI's : Compliance of systems, Accuracy of data, Quarterly metrics.
