
Pharmacovigilance Specialist
Welcome to Eli Lilly and Company, a global pharmaceutical company dedicated to improving the lives of people around the world. We are currently seeking a passionate and experienced Pharmacovigilance Specialist to join our team and support our mission of developing innovative and life-changing medicines. As a Pharmacovigilance Specialist, you will play a critical role in ensuring the safety and effectiveness of our products, while also providing valuable insights to our drug development process. If you have a strong background in pharmacovigilance and a desire to make a positive impact on patient health, we encourage you to apply for this exciting opportunity.
- Monitor and assess safety data for assigned products in compliance with global pharmacovigilance regulations and guidelines.
- Conduct thorough and timely review of adverse event reports and determine their potential impact on the safety profile of our products.
- Collaborate with cross-functional teams to develop and implement risk management plans for our products.
- Serve as subject matter expert on pharmacovigilance regulations and guidelines, providing guidance and support to other team members.
- Conduct periodic signal detection and evaluation activities to identify potential safety concerns and take appropriate actions.
- Maintain accurate and complete documentation of all pharmacovigilance activities, ensuring compliance with company policies and procedures.
- Participate in the development and maintenance of pharmacovigilance-related processes and systems.
- Communicate safety updates and recommendations to internal stakeholders, including senior management.
- Collaborate with external partners, such as regulatory agencies and contract research organizations, to ensure timely and accurate reporting of safety data.
- Continuously stay informed about new pharmacovigilance regulations and guidelines and incorporate them into our processes and procedures.
- Support the development of safety-related documents, including periodic reports, investigator brochures, and risk management plans.
- Provide training and guidance to colleagues on pharmacovigilance best practices and processes.
- Participate in audits and inspections related to pharmacovigilance activities.
- Contribute to the continuous improvement of pharmacovigilance processes and procedures to enhance patient safety and product effectiveness.
Bachelor's Or Master's Degree In Pharmacy, Pharmacology, Or A Related Field.
Minimum Of 2-3 Years Of Experience In Pharmacovigilance Or Drug Safety, Preferably In The Pharmaceutical Industry.
In-Depth Knowledge Of Fda And Global Regulatory Requirements For Pharmacovigilance.
Strong Analytical And Problem-Solving Skills, With The Ability To Critically Evaluate And Interpret Safety Data.
Excellent Communication And Interpersonal Skills, With The Ability To Collaborate Effectively With Cross-Functional Teams And External Stakeholders.
Risk Management
Data Analysis
Regulatory compliance
Medical coding
safety
pharmacology
Clinical Trials
Drug Safety
Adverse Event Reporting
Signal Detection
Pharmacovigilance Systems
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
Interpersonal Skills
creativity
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Pharmacovigilance Specialist in San Diego, CA, USA is $70,000-$90,000 per year. However, salaries can vary based on factors such as experience, qualifications, and the specific company or organization the individual is working for. Additionally, bonuses and benefits may also be included in the total compensation package for a Pharmacovigilance Specialist in San Diego.
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Eli Lilly and Company is an American pharmaceutical company headquartered in Indianapolis, Indiana, with offices in 18 countries. Its products are sold in approximately 125 countries. The company was founded in 1876 by, and named after, Col. Eli Lilly, a pharmaceutical chemist and veteran of the American Civil War.

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