Attention Pharmacovigilance Professionals! Don’t Miss this Job Opening at Accenture

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"Attention Pharmacovigilance Professionals! Don't Miss this Job Opening at Accenture"

Accenture Pharmacovigilance Job Opening – Apply Online

Pharmacovigilance Services Specialist – Pharmacovigilance

Location: BENGALURU

JOB NO. 300872

Job Description

Skill required: Pharmacovigilance – Pharmacovigilance & Drug Safety Surveillance

Designation: Assistant Manager – Pharmacovigilance Services

Job Location: Bengaluru

Qualifications: Bachelor of Pharmacy/Master of Pharmacy

Years of Experience: 7 to 11 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 an 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 Overview/abbreviated Clinical Overview. 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?

• Adaptable and flexible

• Ability to perform under pressure

• Problem-solving skills

• Detail orientation

Roles and Responsibilities

  • In this role, you are required to do analysis and solving of moderately complex problems
  • May create new solutions, leveraging and, where needed, adapting existing methods

Qualifications

Bachelor of Pharmacy/Master of Pharmacy

Link to Original Notification to apply: Apply Here

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