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PhV Scientist

Date: Mar 23, 2021

Location: Netanya, IL, 1111

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

 

Teva Pharmacovigilance (Patient Safety) unit is hiring a PhV Scientist to join the Medical Scientific Unit located in Netanya.

 

The PhV scientist will be responsible for most operational tasks associated with product safety. This will include drafting and negotiating agreements with CRO, assuring that adverse event reports are submitted on time and accordance with applicable regulations, maintaining a pregnancy tracker, and reconciling safety database information with the data management department. Additionally, they will assist the safety physician in preparation of regulatory documents, health authority requests, and preparation of safety database spreadsheets for analysis.  

 

  • Case processing of CT cases, reconciliation and additional related tasks
  • Take part in databases search strategy discussions and be responsible for the data retrieval for safety assessment and evaluation
  • Take part in preparing & providing training / mentoring to newcomers or other MSU members in different topics as required
  • Take part in writing SAE Management Plan and review of the safety reporting section in study protocols
  • Take part in QC of various documents/reports
  • Take part in maintaining trackers for additional risk minimization measures or additional PhV activities
  • Take part in writing safety update periodic reports
  • Provide medical assessment for ICSRs associated with Teva marketed products

Qualifications

 

  • Bachelor Degree in Pharmacy/ nursing or Pharm D
  • Experience in pharmacovigilance is an advantage
  • Good communication skills, analytical capability, writing
  • Assertiveness, ability to work under pressure sometimes with tight deadlines
  • Strong written and verbal English communication skills
  • Flexibility to adapt to shifting team priorities
  • Advanced knowledge of Microsoft Office platforms
  • Details orientation
  • Ability to work collaboratively and effectively in a global team environment

Function

Regulatory Affairs

Sub Function

Pharmacovigilance

Reports To

Sr Dir MSU Team Leader, PhV MSU Management

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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.