Job Description : Facilitates safety monitoring by optimizing scientific quality documentation and data entry of safety case reports for Novartis drugs. Responsible for the receipt, tracking and initialization of single case drug safety reports in to the safety database; accurate data entry and coding of adverse event reports and evaluation of non-expeditable reports within well defined timeframes, in compliance with DS&E business rules, standard operating procedures and regulatory requirements.
Desired Profile : Medical Degree (MBBS) or Bachelors Degree in Pharmacy or Advanced Nursing Degree or Masters Degree in life sciences or related fields; or equivalent combination in educational credentials and experience Preferred : MD or MS in Clinical Pharmacy, PhD in Life sciences .
Languages: Good knowledge/fluency in English. Knowledge of other languages desirable. Experience/Professional requirement:
• Familiarity with medical terminology
• Ability to write clearly and concisely
• Self motivation and proactive stance to work
• Sense of urgency and commitment for timely comple-tion of activities
• Prior Medical Transcription or Medical Writing experi-ence preferred
• Previous safety or clinical trial experience desirable, but not essential
• Previous data entry experience desirable, but not essential
Experience : 1 - 6 Years
Location : Hyderabad / Secunderabad
Keywords : Pharmacovigilance, Single case reporting, Aggregate reporting, RMP
Contact : Novartis Healthcare Pvt Ltd
Website : http://www.novartis.com/
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