New Associate-Pharmacovigilance

Job Description Skill required: Pharmacovigilance - Pharmaceutical Drug Safety Surveillance Designation: Management Level - New Associate Job Location: Bengaluru Qualifications: BSc Years of Experience: 0-1 years About Accenture Operations In today's business environment, growth isn't just about building value-it's fundamental to long-term business survival. So how do organizations sustain themselves? The key is a new operating model-one that's anchored around the customer and propelled by intelligence to deliver exceptional experiences across the enterprise at speed and at scale. You will deliver breakthrough business outcomes for clients-by harnessing talent, data and intelligence to revolutionize their operating models. Operations is one of four services that make up one Accenture -the others are Strategy and Consulting, Interactive and Technology. Visit us at www.accenture.com
What would you do? 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 Pharmacovigilance team which designs and maintains a safety database to monitor single case support activities; source distribution for business partners and perform medical literature searches. Responsible for data entry, MedDRA coding, and label assessment of the adverse events in SUSAR cases. If there are issues with the provided information, the scientist is contacted for verification. Pharmaceutical Drug Safety Surveillance is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products What are we looking for? We are looking for individuals who have the following skillset:

• Medical Writing
• Ability to establish strong client relationship
• Ability to work well in a team
• Ability to handle disputes
• Ability to manage multiple stakeholders

It would be a value add if you are proficient in:

• Pharma ERP

Roles and Responsibilities

• In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines
• Your primary interaction is within your team and your direct supervisor
• You will be given detailed instructions on all tasks that need to be carried out, and the decisions that you make will impact your work
• You will need to be well versed with basic statistics and terms involved in the day to day business and use it while discussing with stakeholders
• You will be working closely with project members to effectively deliver on the requirements
• You will be an individual contributor as a part of a team with a predetermined focused scope of work.
Please note this role may require you to work in rotational shifts.

Qualifications BSc