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Associate, Drug Safety

Mumbai, MH
Job Code:
  • Biotechnology & Science
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Job Details

Job Posting Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or from a clinical trial Maintain a strong understanding of Covance s safety database conventions or client specific database conventions, as appropriate. Begin participating in signal detection and trend and pattern recognition activities, as appropriate. Begin preparing timely pharmacovigilance reports for products and safety issues, including Individual Case Summary Reports (ICSRs) of Serious Adverse Events Assist in the preparation of listings for Annual IND reports, Periodic Reports (PRs) and Periodic Safety Update Reports (PSURs). Work with Data Management or client on reconciliation of safety databases. Begin participating in the generation of monthly status and other project-specific reports ensuring the quality and accuracy of metrics and data provided. Support/train less experienced safety staff in all aspects of case-handling, adverse event reporting. Maintains a comprehensive understanding of Covance Safety s Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance. Possess knowledge of other procedural documents, e.g., SOPs, etc. that impact Safety. Ensure compliant safety reporting in accordance with US and international reporting regulations, SOPs and safety processing guidelines set forth by departmental management team and the client. Build and maintain good PV&DSS relationships across functional units. Demonstrate role-specific Competencies on a consistent basis. Demonstrate company Values on a consistent basis. Begin to develop a good knowledge of contract assumptions; identifying out of scope work. Read and understand Safety Management Plans (SMPs), Reconciliation Plans, and other safety-specific plans ensuring optimal efficiency. Begin participating in Covance project teams and client meetings as appropriate. Assist in the review of cumulative safety data for submission to Drug Safety Monitoring Boards (DSMBs), regulatory authorities or clients. Assist with the set-up of, and the provision of data to, Safety Committees/DSMBs. Assist in the co-ordination of endpoint committees, as required. Any other duties as assigned by management.Education/Qualifications Non-degree + 4-5 yrs relevant experience (or 2 yrs safety experience) Associates Degree + 3-4 yrs relevant experience (or 1-2 yrs safety experience) Associate degree RN + 2-3 yrs relevant experience (or 1-2 yrs safety experience) BS/BA + 1-2 yrs relevant experience MS/MA + 0 yr relevant experience PharmD + 0 yrs relevant experienceDegree preferred to be in one or more of the following disciplines Biological Sciences, Pharmacy, Nursing, Life Sciences, and Chemistry.Experience High degree of accuracy with attention to detail. Functions as a team player. Good Communication. Knowledge of medical and drug terminology desirable. Familiarity of Good Clinical Practice (GCP) related to clinical safety documentation. Familiarity with ICH Guidelines Familiarity of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products. Familiarity of worldwide regulatory requirements and reporting of adverse event for both marketed and investigational products. Good written and verbal communication skills. Ability to work independently with moderate supervision. Good keyboard skills, preferably with knowledge of MS office and Windows would be beneficial.
Additional Degree: BA (Arts) | B.Com. (Commerce) | B.Pharm. (Pharmacy) | B.Plan. (Planning) | B.Sc. (Science) | BBA/ BBM/ BBS | BCA (Computer Application) | Diploma-Other Diploma | B.Ed. (Education) | BHM (Hotel Management)

Experience: 2-5


Basic Research | Clinical Research
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