Tata Elxsi Released Job Openings On 14/12/2021.Tata Elxsi is amongst the worlds leading providers of design and technology services across industries including Automotive, Broadcast, Communications, Industrial design and Healthcare. Tata Elxsi has approx. 9000 employees across 35 plus locations. We started our corporate journey way back in March 1989.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Tata Elxsi Recruitment 2021 are provided below. Interested and eligible candidates can submit application along with resume.Â
Vacancy Details:
Tata Elxsi Recruiting Master/ Bachelor in Pharmacy, Medicine, Nursing or Alternative medicine  Candidates with 0-2 years of experience in Pharmacovigilance is must  for Junior Associate – Pharmacovigilance ( Voice Process) Position.Complete Details for the Junior Associate – Pharmacovigilance ( Voice Process) as follows.
Important Details :
- Location :Mumbai
- No of Vacancies:Not Disclosed By Recruiter
- Details of Salary: Not Disclosed By Recruiter
- Opening date for online Application: 14/12/2021
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job: B.Pharm Jobs For Fresher And Experienced CandidatesÂ
Job Description/Skills Required
- To take telephone calls from consumers/ patients/ HCPs from the US and European regions in a professional and courteous manner
- Identify the customer concern and follow the adverse event, product complaint or medical enquiry call script as applicable
- On receipt of patient call, search computerized patient records, checking patient details and patient confidentiality and create initial or follow up case as applicable
- Maintaining confidentiality at all times with particular reference to patient confidentiality and Data Protection Act
- Identify callers requiring an immediate emergency response and refer to appropriate department
- Taking care of rapid and timely processing of new and follow-up reports of adverse events as well as Serious Adverse Events (SAE’s) both from Post-marketing safety programs and Clinical Trials, Product Complaints and Medical Inquiries
- Performs outbound calls as per agreed process
- Quality check of the information filled in the case in the safety database
- Ensure that the productivity targets are met and delivered within timelines
- Understand and comply with Standard Operating Procedures (SOPs), Work Instructions (WIs), global drug/biologic/device regulations, Good Clinical Practices (GCPs), ICH guidelines, Good Pharmacovigilance Practice (GVP) modules, study plans and the drug development process
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