Medical Advisor

2 weeks ago

Budapest, Hungary TATA Consultancy Services Hungary Full time
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  • Enter reports of drug adverse events from post-marketed or clinical study source to the safety database.
  • Provide medical expertise and judgment throughout the case-handling process with medical review of individual cases.
  • You will handle non-serious and serious cases according to regulatory requirements, process instructions and standard operational procedures.
  • Resolves queries related to pharmacovigilance activities and individual case reports.
  • Adhere to global and local procedural documents.
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  • A Medical or Physician Degree.
  • Good knowledge of US and EU pharmacovigilance regulatory requirements.
  • Experience in pharmacovigilance practices concerning signal detection and evaluation.
  • Knowledge of drug safety and clinical development and ICH/GCP principles.
  • The ability to evaluate, interpret and synthesize scientific data.
  • The ability to present and critically discuss clinical data in both internal and external discussions.
  • User-level IT skills.
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  • TCS has been delivering services from Hungary since 2001, making us the perfect choice offering stability
  • We provide a wide range of benefits, including a market-leading comprehensive private health care package
  • We offer extensive self-development opportunities: our colleagues have many training possibilities for personal and professional growth
  • At TCS Hungary there are both vertical and horizontal career options for those who like to challenge themselves and try out different areas and positions
  • You will be part of a global and diverse working environment with relaxation areas, terraces, and a friendly atmosphere
  • You can seize the day with us at our company events, hobby clubs, and sporting initiatives
  • An attractive compensation package