Accenture Hiring Pharmacovigilance Jobs Fresher

Accenture Hiring Drug Safety Associate | B.Pharm, B.Sc & B.Sc Nursing Apply Online

Accenture is inviting applications for the position of Drug Safety Associate under its Pharmacovigilance Services division. This opportunity is suitable for candidates with a background in B.Pharm, B.Sc, and B.Sc Nursing who are looking to build a career in pharmacovigilance and drug safety. Candidates with 1–3 years of experience can apply for this full-time position based in Bengaluru. Interested applicants can check the eligibility criteria, job responsibilities, and application process below.

Job Description

Job Title: Drug Safety Associate

Department: Pharmacovigilance Services

Job Type: Full Time

Job Location: Bengaluru

Job ID: AIOC-S01655657

Experience Required: 1–3 Years

Qualification: B.Sc, Bachelor of Pharmacy (B.Pharm), B.Sc Nursing

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.
  • Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products. These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients.
  • The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements. Effective pharmacovigilance services are essential for maintaining public trust in medications.
  • 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?

  • Pharmacovigilance Services involve the detection, assessment, and prevention of adverse effects related to pharmaceutical products.
  • These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients.
  • The goal is to identify potential risks and take appropriate actions to protect patient health. They also help pharmaceutical companies comply with regulatory requirements.
  • Effective pharmacovigilance services are essential for maintaining public trust in medications.
  • 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.

Roles and Responsibilities:

  • In this role you are required to solve routine problems, largely through precedent and referral to general guidelines
  • Your expected interactions are within your own team and direct supervisor
  • You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
  • The decisions that you make would impact your own work
  • You will be an individual contributor as a part of a team, with a predetermined, focused scope of work• Please note that this role may require you to work in rotational shifts

 

How to Apply

Interested and eligible candidates can apply online through the official application link below.

Apply Here:

Tagged as: Case Processing, Clinical Trials, Drug Safety, MedDRA, Qualification

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