Accenture Analyst-Pharmacovigilance Post Vacancy – M Pharma Apply

Accenture Analyst-Pharmacovigilance Post Vacancy - M Pharma Apply

Accenture Analyst-Pharmacovigilance Post Vacancy – M Pharma Apply

Accenture job opening 2022, M Pharma job opening 2022. M Pharma job opening 2022. Senior Analyst-Pharmacovigilance job opening 2022. Pharmacovigilance pharma job opening 2022. Pharmacovigilance pharma job opening 2022. Candidates with a bachelor’s degree in pharmacy may apply for the job opening at Accenture

Job Title: Senior Analyst-Pharmacovigilance

Job Location: Bengaluru

JOB NO. 187667

Skill required: Pharmacovigilance – Clinical & Regulatory Writing

Qualifications: Master of Pharmacy

Years of Experience: 5-8 years

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 reviewing and resolving discrepancies identified by the system or through manual checks 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 part of a dynamic Pharmacovigilance team with array of capabilities ranging from detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem following Good Pharmacovigilance Practice (GVP) per client SOPs and applicable global regulatory requirements (Individual Case Safety Reports) to working on various aspects of Aggregate reports such as planning, authoring, reviewing and publishing of PBRER, PSUR, DSUR, PADER, Addendum to clinical overview (AdCO), Risk Management Plan (RMP), Signal detection and validation reports (SDVR), Cosmetovigilance Safety Reports (CoSR). The Pharmacovigilance team is also responsible for authoring and reviewing clinical documents such Protocols and amendments, Investigator brochures, Clinical Study Reports (CSR), Synoptic/Abbreviated CSR, Safety Narratives, Clinical Overview/abbreviated Clinical Overview.
  • In this role, you will be expected to produce variety of clinical documents throughout the lifecycle of a (potential) treatment, starting with describing and reporting data from clinical trials, through to preparing regulatory submission documents including post approval reports.

What are They looking for?

They are looking for individuals who have the following skillset:

  • Ability to perform under pressure
  • Ability to work well in a team
  • Ability to manage multiple stakeholders
  • Ability to meet deadlines

Roles and Responsibilities

  • In this role, you need to analyze and solve increasingly complex problems
  • Your day-to-day interactions is with peers within Accenture
  • You are likely to have some interaction with clients and/or Accenture management
  • You will be given minimal instruction on daily work/tasks and a moderate level of instructions on new assignments
  • You will need to consistently seek and provide meaningful and actionable feedback in all interactions
  • You will be expected to be constantly on the lookout for ways to enhance value for your respective stakeholders/clients
  • Decisions that are made by you will impact your work and may impact the work of others
  • You would be an individual contributor and/or oversee a small work effort and/or team.

Editors Note: Accenture Analyst-Pharmacovigilance Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.

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