Pharmacovigilance Services Analyst-Vacancy for BPharm, MPharm MSc graduates and postgraduate at Accenture, CHENNAI

  • Clinical Research jobs
  • Chennai

Website Accenture

Pharmacovigilance Services Analyst-Vacancy at Accenture , CHENNAI

JOB NO. AIOC-S494271


Skill required:

  • Pharmacovigilance –
  • Safety Writing

Designation: Senior Drug Safety Associate

Job Location: Chennai

Qualifications: MSc/Bachelor of Pharmacy/Master of Pharmacy

Years of Experience: 3 to 5 years

About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries.

We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.

What would you do?

You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions.

Employees under this span will be a part of one of the sub-offerings –
Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.

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 amendment, Investigator Brochure, Clinical Study Reports (CSR), Synoptic/Abbreviated CSR, Safety Narratives, Clinical O In this role, you will be expected to manage and develop individual case narratives describing adverse events for inclusion in regulatory submissions and safety reports for completed/interim clinical study reports.

What are we looking for?

  • • Ability to establish strong client relationship
  • • Ability to perform under pressure
  • • Adaptable and flexible
  • • Problem-solving skills MSC Life Science Roles and Responsibilities
  • • In this role you are required to do analysis and solving of lower-complexity problems
  • • Your day to day interaction is with peers within Accenture before updating supervisors
  • • In this role you may have limited exposure with clients and/or Accenture management
  • • You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments
  • • The decisions you make impact your own work and may impact the work of others
  • • You will be an individual contributor as a part of a team, with a focused scope of work
  • • Please note that this role may require you to work in rotational shifts

Last date: 15 June 2024

For more detail: Click Here

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