About this role
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.
Your role:
You will join our Global Patient Safety ICSR Management team in the R&D Excellence Center Bangalore. Your key responsibilities in your role are:
- to support of the business process owner for the literature surveillance process.
- to support training documentation and user access management in the literature surveillance database and reconciliation management database.
- operational management activities in the literature surveillance database such as reconciliation, QC of non-ICSR literature or the upload of articles.
- Perform ICSR reconciliation, quality monitoring and spot check of safety information with the relevant functions.
- Handles the team mailboxes and ensure that all the mails received are actioned on time.
Who you are:
- Medical/scientific degree and at least 3 years of experience in the pharmacovigilance environment - ideally, you have worked in the literature safety surveillance process and in ICSR Reconciliation before.
- You have a sound understanding of regulations relevant to the safety of drugs in development and post-authorization.
- Ideally ICSR Case processing experience in ArisG safety Database environment
- Good communication skills and experience in an international environment are equally important as intercultural experience through successful collaboration in matrix teams.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!
Other facts
About The businesses of Merck KGaA, Darmstadt, Germany
We are Merck KGaA, Darmstadt, Germany and its global affiliates. We are a leading global science and technology company headquartered in Germany.
We are curious explorers, courageous pioneers, and ingenious inventors. Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Life Science, Healthcare, and Electronics.
Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and the planet.
We believe in the positive power of science and technology. It has determined our actions since 1668 and inspires us to continue researching for a future worth living. As a family-owned company with over 350 years of experience, we stand for sustainability, responsibility, and innovative strength.
We take pride in being a diverse and inclusive company that values and fosters the talents and abilities of our employees. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Privacy Statement: https://www.emdgroup.com/en/privacy-statement.html
What you'll do
- The role involves supporting the literature surveillance process and managing operational activities in the literature surveillance database. Responsibilities also include ICSR reconciliation and quality monitoring of safety information.
Ready to join The businesses of Merck KGaA, Darmstadt, Germany?
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