https://bayt.page.link/PiUuJe65bzyihzsA6
أنشئ تنبيهًا وظيفيًا للوظائف المشابهة

الوصف الوظيفي

Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region. The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions. Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the company.


Main job responsibilities:


  • Monitoring the safety profiles of our marketed products and addressing any
  • emerging safety concern
  • Prepare and Submit PV New Drug/Device Application
  • file, PV Renewal file, PSUR, RMP, ACO, SMH and any other Pharmacovigilance & Device Vigilance related files to EDA.
  • Conducting pharmacovigilance training for internal employees and external partners and onboarding new employees, and communicating Safety requirements to business partners and assisting them in their implementation
  • Handling pharmacovigilance cases, customer complaints, and adverse events for marketed products and ensuring the overall compliance of PV activities to the local and global regulations as applicable.
  • Ensuring compliance with local and global regulations related to pharmacovigilance activities, and safety reporting for clinical trials.
  • Collaborating with the pharmacovigilance team at our headquarter

Qualification


  • 3-5 years in pharmacovigilance
  • Bachelor’s degree in pharmacy
  • Certified QPPV to work with EDA
  • ICSR end-to-end processing skills
  • Experience in all aspects of drug safety
  • Strong analytical and problem-solving abilities.
  • Excellent communication skills, both written and verbal.
  • Proficiency in safety database tools and MS Office.
  • Knowledge of Egyptian and global pharmacovigilance regulations.
  • Attention to detail and high accuracy in data handling.
  • Ability to work independently and meet deadlines under pressure.
  • Team-oriented mindset with strong organizational skills.
  • Commitment to patient safety and ethical standards.
  • Experienced with drug safety databases like Argus Aris G or PV247 or eve Drug data base

لقد تجاوزت الحد الأقصى لعدد التنبيهات الوظيفية المسموح بإضافتها والذي يبلغ 15. يرجى حذف إحدى التنبيهات الوظيفية الحالية لإضافة تنبيه جديد
تم إنشاء تنبيه للوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.
تم إلغاء تفعيل تنبيه الوظائف المماثلة بنجاح. يمكنك إدارة التنبيهات عبر الذهاب إلى الإعدادات.