Pharmacovigilance Services Associate Opportunity at Accenture! Apply Now!
"Unlock Your Career: Pharmacovigilance Services Associate Opportunity at Accenture! Apply Now!"

Pharmacovigilance Services Associate Opportunity at Accenture! Apply Now!

Pharmacovigilance Services Associate

Bengaluru | Job No. aioc-s01549698 | Full-time

Job Description

Skill required: Pharmacovigilance Services – Pharmacovigilance & Drug Safety Surveillance

Designation: Pharmacovigilance Services Associate

Qualifications: Bachelor of Pharmacy

Years of Experience: 1 to 3 years

Language – Ability: English – Advanced

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. Visit us at www.accenture.com.

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 in 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 by improving outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.

  • Management of the Affiliate Mailbox
  • Reconciliation of reports per process
  • Performance of all written follow-up attempts to include both Serious and Non-serious cases

In this role, you will be expected to create and manage:

  • Case identification
  • Data entry
  • MedDRA coding
  • Case processing
  • Submission and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements

What are we looking for?

  • You are required to solve routine problems, largely through precedent and referral to general guidelines
  • Expected interactions are within your own team and direct supervisor
  • You will be provided detailed to moderate levels of instruction on daily work tasks and detailed instruction on new assignments
  • The decisions you make would impact your own work
  • You will be an individual contributor as part of a team, with a predetermined, focused scope of work

Please note that this role may require you to work in rotational shifts.

Qualifications: Bachelor of Pharmacy

To apply for this position, please visit the original notification.

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