TCS Hiring Life Sciences For Drug Safety Specialist Vacancy, Apply Online

TCS Drug Safety Specialist Vacancy For Life Sciences, Apply Online

TCS Drug Safety Specialist Vacancy For Life Sciences, Apply Online. Graduate and Postgraduate life sciences candidates apply for a Drug Safety Specialist vacancy at Tata Consultancy Services. TCS Mumbai Drug Safety Specialist job opening. Interested and eligible applicants can check out all of the details on the same below

Wondering what kind of interview questions can be asked? Then read further 

Drug Safety Specialist

Location – Tata Consultancy Services Mumbai, Maharashtra, India On-site

Skill – Pharmacovigilance – Drug Safety

Work location: Mumbai/ Pune/ Indore

Job Description:

• Analyses and Process case (ICSR) related data
• Contribute in Implementation of “New Safety Systems, SOPs & Processes”
• Excellent communication skills (verbal and written)

Education Criteria: Graduate/Postgraduate in Life Sciences/Pharmacy, Degree in Alternate Medicine, Bachelor/Master in Dentistry

Experience: 1 – 7 years of relevant experience in Pharmacovigilance

A purpose-led organization that is building a meaningful future through innovation, technology, and collective knowledge. We’re #BuildingOnBelief.

A part of the Tata group, India’s largest multinational business group, TCS has over 500,000 of the world’s best-trained consultants in 46 countries. The company generated consolidated revenues of US $22.2 billion in the fiscal year ended March 31, 2021, and

is listed on the BSE (formerly Bombay Stock Exchange) and the NSE (National Stock Exchange) in India.

TCS’ proactive stance on climate change and award-winning work with communities across the world have earned it a place in leading sustainability indices such as the MSCI Global Sustainability Index and the FTSE4Good Emerging Index.

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POSSIBLE INTERVIEW QUESTIONS AT TCS FOR DRUG SAFETY SPECIALIST ROLE

1. Can you tell us about your experience with pharmacovigilance and drug safety?
   Answer: Yes, I have 3 years of experience in pharmacovigilance and drug safety. During my tenure, I have worked on ICSR data analysis and processing. I have contributed to the implementation of new safety systems, SOPs, and processes. Additionally, I have excellent verbal and written communication skills.
2. What is your experience with new safety systems implementation, and how did you contribute?
   Answer: During my previous job, I was a part of a team that implemented a new safety system. My role involved reviewing the system and ensuring that it was functioning correctly, training the team members on the new system, and updating SOPs and processes as needed.
3. Can you describe your knowledge of pharmacovigilance regulations?
   Answer: Yes, I have a strong understanding of pharmacovigilance regulations, including ICH guidelines and regulatory requirements for different regions like FDA, EMA, etc. I keep myself updated with the latest developments in pharmacovigilance regulations.
4. Can you give an example of how you have improved the pharmacovigilance process in your previous role?
   Answer: In my previous role, I identified a process bottleneck, which was causing delays in the case processing. I proposed a solution to automate the process, which led to a significant reduction in processing time and improved efficiency.
5. How do you prioritize your work when dealing with a high volume of cases?
   Answer: When dealing with a high volume of cases, I prioritize them based on their urgency and severity. I ensure that cases with serious or unexpected adverse events are given top priority, while cases with less critical issues are processed promptly. Additionally, I maintain effective communication with my team and stakeholders to ensure that we are aligned with our priorities.

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