
Pharmacovigilance Specialist
Are you passionate about ensuring the safety and efficacy of pharmaceutical products? Do you thrive in a fast-paced, dynamic environment? If so, we have an exciting opportunity for you at Eli Lilly and Company as a Pharmacovigilance Specialist. As a global leader in the pharmaceutical industry, we are dedicated to improving patient outcomes and making a positive impact on healthcare. We are looking for a highly motivated and detail-oriented individual to join our team and play a key role in monitoring and reporting adverse events associated with our products. If you have a strong background in pharmacovigilance and a commitment to upholding the highest standards of drug safety, we encourage you to apply.
- Monitor and evaluate adverse events associated with pharmaceutical products.
- Conduct thorough and timely investigations into adverse events, including medical and scientific evaluations.
- Maintain accurate and up-to-date records of adverse events and pharmacovigilance activities.
- Collaborate with cross-functional teams, including medical, regulatory, and quality, to ensure comprehensive assessment and reporting of adverse events.
- Stay current with relevant regulations and guidelines related to pharmacovigilance, and ensure compliance with all applicable laws and regulations.
- Review and analyze safety data, and provide recommendations for risk management and mitigation strategies.
- Communicate safety findings and recommendations to internal and external stakeholders, including healthcare professionals and regulatory agencies.
- Participate in the development and implementation of pharmacovigilance processes and procedures to ensure adherence to company standards and regulatory requirements.
- Conduct training and education sessions for internal employees and external partners on pharmacovigilance practices and procedures.
- Participate in safety review meetings and committees, providing expert insights and recommendations for product safety.
- Contribute to the continuous improvement of pharmacovigilance processes and systems to enhance efficiency and effectiveness.
- Adhere to ethical standards and maintain confidentiality of all pharmacovigilance information.
- Serve as a subject matter expert on pharmacovigilance topics, and provide guidance and support to colleagues and team members.
- Foster a culture of drug safety and compliance within the organization.
Strong Analytical And Problem-Solving Skills
Bachelor's Or Master's Degree In Pharmacy, Medicine, Or Related Field
Knowledge Of Pharmacology, Drug Safety, And Regulatory Requirements
Minimum Of 3-5 Years Of Experience In Pharmacovigilance Or Drug Safety
Excellent Communication And Interpersonal Skills, With The Ability To Work Effectively In A Cross-Functional Team Environment.
Data Analysis
Drug development
Risk assessment
Regulatory compliance
pharmacology
Clinical Trials
Medical Writing
Drug Safety
Safety Reporting
Drug
Signal Detection
Adverse Events
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
Critical thinking
Teamwork
collaboration
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Pharmacovigilance Specialist in Charlotte, NC, USA is between $75,000 and $100,000 per year. However, this range can vary depending on factors such as experience, education, and specific job duties. Some Pharmacovigilance Specialists may earn higher salaries in this area if they have advanced degrees or extensive experience in the field. Additionally, salaries may also be influenced by the specific company or organization the specialist works for.
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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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