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Lilly Coordinador de farmacovigilancia LACAM in Buenos Aires, Argentina

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Main responsibilites:

Maintain local and regional pharmacovigilance standard operating procedures (SOP) in aligned with Global Patient

Safety (GPS) procedures and other guidelines provided by GPS with help of the Medicines Quality Consultant.

 Keep LATAM (excl. BR and Mexico) employees updated on regulations and changes, which may impact the local and

regional adverse event (AE) reporting process.

 Provide training and consultation on pharmacovigilance process to Regional personnel with responsibilities related to

reporting of adverse events.

 Be compliant with training requirement for this position.

 Assist in audits and inspections and follow-up appropriately.

 Responsible for appropriate communications between Patient Safety locally, regionally and globally, and with Product

Complaint organization, Medical and Regulatory Affairs.


Education, preferably university degree, in medicine, pharmacology, pharmacy, medical, biology, biochemistry, physiology,

or comparable education/experience.

 Deep knowledge in Pharmacovigilance concepts thoroughly trained in this area.

 Knowledge of local and regional law and international guidelines regarding drug safety

 Effective communication skills to interact with diverse groups and individuals.

 Fluent in written and spoken English.

 Have excellent interpersonal, oral and written communication skills.

 Be able to work in a team and have no personality problems that are incompatible with this critical function.

 Computer literacy is necessary and would be considered an asset. Knowledge of Word, Excel, Windows and other

informatics tools.

 Training skills.

 Knowledge and understanding of Good Pharmacovigilance Practices and Clinical Safety Data Management Guidelines

from ICH, CIOMS, Argentinean and Regional regulations

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!