Covance Safety Science Coordinator Recruitment - Apply Online

Covance Safety Science Coordinator Recruitment – Apply Online

Covance Pharma Jobs. B Pharma candidates are encouraged to apply online for the Safety Science coordinator vacancy that is available at Covance. Covance Bangalore Job openings for Pharma & Chemistry candidates. Check out all of the details on our website

Job Title: Safety Science Coordinator 2

Location Bangalore, India

Job ID: 59074

Job Overview:

  • Assist in or complete per the Safety Management Plan (SMP) the processing of all adverse event reports from any source.
  • Assist in producing queries of safety data for clients as appropriate.
  • Assist in the generation and maintenance of the PV&DSS metrics.
  • Assist Data Management or clients on reconciliation of safety databases.
  • Provide input for monthly status reports.
  • Maintains a comprehensive understanding of 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, and how they impact safety.
  • Build and maintain good PV&DSS relationships across functional units.
  • Demonstrate role-specific Core Competencies on a consistent basis.
  • Demonstrate company values on a consistent basis.


Non-degree+ 3 yrs relevant experience** (or 1 yr safety experience)*
Associates Degree + 2 yrs relevant experience** (or l yr safety experience)*
Associate degree RN + 1 yr relevant experience**
BS/BA + 0 yrs

Degree preferred (but not necessary) to be in one or more of the following disciplines:  Pharmacy and Chemistry.

*Safety experience includes actual experience processing AE/SAE repo1ts, generating narratives, queries, working within safety databases, and experience with regulatory submissions.

**Relevant experience includes experience in the pharmaceutical, biotechnology, or CRO industry, paitly in related areas such as Medical Affairs, Clinical Data Ently and Clinical Data Management, Clinical Data Monitor, Regulatory Affairs, or Quality Assurance.


  • The high degree of accuracy with attention to detail.
  • Functions as a team player.
  • Good communication.
  • Good written and verbal communication skills.
  • Ability to work independently with moderate supervision.
  • Good keyboard skills with knowledge of MS Office and Windows applications would be beneficial.

Apply Online

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