Pharmacovigilance Regulatory affairs Job @ Accenture

Pharmacovigilance Regulatory affairs Job @ Accenture

Accenture Pharmacovigilance Regulatory affairs. Accenture invites postgraduate and undergraduate Pharma candidates for the post of Regulatory affairs. Interested and Eligible candidates may grab this opportunity by applying online. Check out all the details on the same below:

Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions —underpinned by the world’s largest delivery network

Job Title: Pharmacovigilance Regulatory affairs

JOB NO. 13141

Job Skill: Regulatory affairs

Designation: Career Level – 11-Analyst

Job Location: Hyderabad

Qualifications: Any Graduation

Years of Experience: 3-5 years

Job Summary

  • You will be aligned with our Pharmaceuticals Processes vertical and help us with the processes to collect, monitor, research, assess and evaluate information on the adverse effects of medication with a view to identifying new information about hazards associated with medicines and consequently, prevent harm to patients. It also deals with the reviewing and resolving of discrepancies identified by the system or through manual checks as per guidelines. Employees under this span can also be responsible for a number of activities related to the design, development, and maintenance of Clinical Database objects.
  • You will be working as a part of the Pharmacovigilance team which designs and maintains a safety database to monitor single case support activities; source distribution for business partners and to perform medical literature searches. Responsible for data entry, MedDRA coding and label assessment of adverse event in SUSAR cases. If there are issues with the provided information, scientist is contacted for verification.
  • You will be responsible for Regulatory affairs wherein you will be accountable for the design, development and delivery of business solutions related to the regulatory review and approval of pharmaceutical drugs and perform publishing and quality control tasks on submission components. You will be creating and maintaining project documentation including meeting agendas, meeting minutes, issues and status reports internally and externally.

Roles and Responsibilities

In this role you are required to do analysis and solving of lower-complexity problems. Interaction is with peers within Accenture before updating supervisors. Likely has limited exposure with clients and/or Accenture management. Moderate level instruction on daily work tasks and detailed instructions on new assignments would be provided. Decisions impact own work and may impact the work of others. Individual contributor as a part of a team, with a focused scope of work.

Apply Online

Editor’s Note: Regulatory affairs Job Opening, B Pharma job opening 2019, M Pharma job opening 2019, Pharmaceutical science jobs at Accenture, Subscribe to Rasayanika for latest chemistry and Pharma job openings.



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