About this role
## We Are Teva
We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
## Our Team, Your Impact
This section is where we attract the attention of potential candidates and sell the role. How has the role come about? What makes it appealing? What are the key responsibilities? How is the role better with Teva than with another company? Wherever possible, we should bring through the essence of our EVP pillars, i.e., we care, we’re in it together, and we make work fulfilling.
## How You’ll Spend Your Day
- Processing serious & non-serious adverse events from various post-marketing sources.
- Ensure accurate and consistent medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in Safety Database.
- Data verification between source documents and entered data in Safety Database for evaluation of events/suspect drug coding, seriousness, causality, listedness and narrative writing.
- Evaluate the need for follow-ups, queries with various stakeholders for correct and accurate data transfer to various parties.
- Ensure that quality data is analyzed for any trending and to prepare team for process stabilization.
- Providing administrative support by taking up complete responsibility of assigned case processing related activities on day-to-day basis.
- Coordinate with internal/ external stakeholders to obtain necessary information required for day-today operations and to update the reporting manager on status reports on real time basis.
- Effective communications to be maintained with internal (related departments and units) & external (partners, authorities, vendors) stake holders in order to run the process as transparent as possible.
- Assist in Safety Database related administrative and procedural activities as required or requested and to ensure that all assigned tasks are performed in compliance in accordance to the work instructions and GVP modules.
- Ensure that quality of case processing and assigned tasks are evaluated and trends are identified for process improvement.
- Various compliance metrics like case timelines, assigned trainings, and TAT for assigned activities are met.
- Provide the analytical support to the peers and managers for investigations & analysis of various trends as a part of audits, and inspections.
- Mentoring/Training the new hires with case processing knowledge transfer, evaluating their progress close to perfection during their initial phases of learning curves.
## Your Skills and Experience
- M.Pharm, Pharm D, B.Pharm, BDS education
- Extensive knowledge of medical terminology, clinical pharmacology, patent treatment, diagnostic investigations and pathology.
- Sound knowledge of pharmacovigilance principles and international regulatory requirements related to drug and patient safety.
- Basic knowledge on TEVA product portfolio, their therapeutic areas expertise, mechanism of actions and its product/patient safety index.
- Possess excellent communication skills with professional English speaking, writing, presenting skills and must be detail oriented.
## Also Good to Have
## Salary Range
## How We’ll Take Care of You
At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.
## Already Working @Teva?
Make sure to apply through our internal career site on Twist—your one-stop shop for career development
## Teva’s Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.