Want to work in an environment that will nurture your professional development? Come and join Teva on its journey of growth. Teva has been cultivating excellence for over a century, and is, today, a worldwide leading generic pharmaceutical company and one of the top 10 pharmaceutical companies in the world. As a forward-looking global pharmaceutical company, Teva spearheads the development, production and marketing of a wide range of specialty, generic and over-the-counter medicines.
With 46,000 employees in 60 countries worldwide, we are proud to say that our employees are the reason for our sustained success. Their skills and dedication make us an industry leader. The diversity of perceptions, qualifications and talent are the key to our ongoing accomplishments. We offer a wide range of jobs and genuine opportunities for personal and professional advancement.
Teva Pharmaceutical Industries Ltd. (NASDAQ:TEVA) is a leading global pharmaceutical company, committed to increasing access to high-quality healthcare by developing, producing and marketing affordable generic drugs & Innovative and specialty pharmaceuticals and active pharmaceutical Ingredients. Headquartered In Israel, leva Is the world's largest generic drug maker, with a global product portfolio of more than 1,250 molecules and a direct presence in approximately 60 countries. Teva employs about 40,000 people around the world and reached $13.9 billion in net sales in 2009.
Designation Drug Safety Associate
Description about work Overview - This position will be hired either at the Drug Safety Associate or Specialist level depending on the experience of the candidate. - This role assists with or leads complex projects as assigned in addition to daily case processing of ADE reports. Functions as a team resource. - Strong emphasis in clinical trial background - Supporting Safety Physicians in activities related to safety review or analysis of the product they are assigned to, either by retrieval of information from the PhV database on request (ad hoc queries) Participating in DSUR preparations of the product he/she is assigned to: including writing (e.g. providing tables), reviewing and distribution. - Preparing Periodic Line Listing document - Responsible to coordinate responses to Health Authority requests
Responsibilities 1. Fully participates in daily case processing activities and assist other associates with case and workflow management. Participates in QC activities. 2. Manages activities in specific projects as assigned. These projects may include but are not limited to electronic submission, creating Cognos reports, periodic report processing, SDEA contracts, REMS participation. 3. Interfaces with other departments to facilitate information exchange and communicates information to ensure clear and consistent reporting. 4. Creates or updates SOP/WI as required by manager. 5. Trains and mentors new associates. Follows Teva Safety, Health, and Environmental policies and procedures Other projects and duties as required/assigned
Essential Qualification required : Bachelor of Science in a health discipline or equivalent combination of education and experience, Preferred: RN, BSN.
Minimum of 2-5 years of drug safety or clinical trials safety reporting experience, Preferred: Drug safety experience in pharma industry setting Note:
Experience: 3 Years Requisition#: 16-16232 Location: US-PA-Horsham Category: Pharmacovigilance