Freshers | Accenture in Pharmacovigilance

Freshers | Accenture in Pharmacovigilance

About Company:
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.

Position Name:
Fresher | Pharmacovigilance Services New Associate

Organization:
Accenture

Qualification:
B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences

Experience:
0 years / Freshers – 1 Year

Salary:
₹25,000 – ₹35,000 /month

Location:
Bangalore

Job Details:

Field	Details
Position	Fresher | Pharmacovigilance Services New Associate
Qualification	B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences
Experience	0 years / Freshers – 1 Year
Salary	₹25,000 – ₹35,000 /month
Location	Bangalore
Vertical	Life Sciences R&D
Date Posted	10/07/2024

Job Description:
You will be aligned with our Life Sciences R&D vertical. Our services span 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.

Responsibilities:

• Manage the Affiliate Mailbox
• Reconcile reports per process
• Perform all written follow-up attempts for both Serious and Non-serious cases
• 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 We Are Looking For:

• Life Sciences background
• Adaptable and flexible
• Ability to perform under pressure
• Ability to work well in a team
• Commitment to quality
• Strong written and verbal communication
• Pharmacovigilance & Drug Safety Surveillance skills
• Clinical Data Management skills

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