
Associate Director, Pharmacovigilance Safety (Fixed-term contract)
Are you a highly experienced and dedicated Pharmacovigilance professional looking for an exciting new opportunity? Look no further! Teva Pharmaceutical USA is seeking a dynamic and motivated Associate Director to join our team on a fixed-term contract basis. In this role, you will play a crucial role in ensuring the safety and effectiveness of our pharmaceutical products. We are looking for an individual with a strong background in Pharmacovigilance and a passion for improving patient outcomes. If you possess excellent leadership skills, a keen attention to detail, and a commitment to upholding industry regulations, we want to hear from you!
- Oversee and manage all aspects of pharmacovigilance activities within Teva Pharmaceutical USA.
- Develop and implement strategies to ensure the safety and effectiveness of pharmaceutical products.
- Lead and mentor a team of pharmacovigilance professionals, providing guidance and support to ensure high-quality work.
- Conduct regular reviews and audits to ensure compliance with industry regulations and company standards.
- Collaborate with cross-functional teams to gather and analyze safety data and identify potential risks or issues.
- Manage and maintain relationships with external stakeholders, such as regulatory agencies and vendors.
- Stay updated on industry trends and regulatory requirements, and make recommendations for process improvements and updates.
- Develop and maintain SOPs and other relevant documents to ensure consistent and efficient pharmacovigilance processes.
- Act as the primary point of contact for all pharmacovigilance-related inquiries and escalations.
- Participate in clinical trial activities, including protocol development, safety monitoring, and study risk assessments.
- Represent the company at external meetings and conferences to share best practices and stay informed on industry developments.
- Support the development and review of pharmacovigilance training programs for employees and external partners.
- Continuously assess and improve pharmacovigilance processes and systems to ensure timely and accurate reporting of adverse events.
- Collaborate with other departments, such as medical affairs and regulatory affairs, to ensure alignment on safety-related matters.
- Act as a subject matter expert on pharmacovigilance and provide guidance to cross-functional teams as needed.
Bachelor's Degree In Pharmacy Or Related Field With A Minimum Of 5 Years Of Experience In Pharmacovigilance Or Drug Safety.
Strong Knowledge Of Fda Regulations And International Pharmacovigilance Guidelines.
Excellent Communication And Leadership Skills To Effectively Manage A Team And Collaborate With Cross-Functional Departments.
Experience In Developing And Implementing Pharmacovigilance Processes And Procedures.
Ability To Multitask And Prioritize Tasks In A Fast-Paced Environment, While Maintaining Attention To Detail And Accuracy.
Risk Management
Quality Assurance
Drug development
Case management
Regulatory compliance
Clinical Trials
Drug Safety
Pharmacovigilance
Safety Reporting
Signal Detection
Adverse Events
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Associate Director, Pharmacovigilance Safety (Fixed-term contract) in Bucharest, Romania is between 5,000 and 8,000 Romanian Lei per month. This converts to approximately $1,188 to $1,901 USD per month. However, salaries may vary depending on the specific company, level of experience, and other factors.
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Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S. Teva Pharmaceutical Industries Ltd. engages in the provision of pharmaceutical services. It operates through the following business divisions: Generic, Specialty Medicine, and Over-the-Counter (OTC).

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