Pharma Jobs at Tata Consultancy Services (TCS) & Wipro

Job Description

Role-Team Member- Pharmacovigilance (PV) – Case Processor

Required Domain Skill Set- Triage and Prioritize cases

Location of Requirement- Mumbai/Pune/Indore/Chennai

Responsibilities-

• Triage and Prioritize cases
• Full data entry of all relevant information from the source data
• Manual coding of all codeable terms (that did not auto-encode), including adverse events, medical history, concomitant medications, and laboratory values
• Complete narratives for ICSRs based on Client GLPS’s auto-narrative templates and conventions
• Workflow Monitoring activities which include – Retrieving daily workflow reports and ensuring users are completing cases nearing the 7/15-day timelines
• Monitoring compliance by identifying and prioritizing expedited cases upto completion
• Review impacted cases daily and escalate/re-route cases to ensure follow up processing is initiated and completed in a timely manner;
• Monitor and maintain record of data correction requests including impact and actions taken.

Location Mumbai

1 – 4 years of experience

Job Function BUSINESS PROCESS SERVICES

Role Scientist

Job Id 273618

Desired Skills LS – Pharmacovigilance

Desired Candidate Profile

Qualifications : BACHELOR OF PHARMACY

Wipro is hiring for Medical & Scientific Writer – M.Pharm, B.Pharm, Pharm.D Apply

Post : Medical & Scientific Writer

Job Description :

1. Reviewing the published reports/biomedical literature to ascertain if they contain a case report of an adverse reaction and Non-individual case reports.
2. Applying regulatory and internal guidance to determine if the article meets the definition of a case report and Non-individual case reports.
3. Write accurate and concise summaries that capture the key elements from these published reports.
4. Ensure consistent coding of medical history, drugs and adverse event terms.
5. Evaluation of Serious Adverse Event to ensure accurate processing from source documents with emphasis on quality and timelines.
6. Creating summary content in a range of formats (narrative summaries, structured database inputs, electronic formats for regulatory filing) to support the drug safety reporting and information requirements of Pharma industry client.
7. To contribute/support the project through query resolution of peer team members.
8. To perform other responsibilities delegated by the team lead/manager.

Technical / Functional Competency :

1. Sound knowledge of regulatory guidelines related to PV domain.
2. Narrative Writing
3. MeDRA Coding
4. Sound knowledge of Pharmacological concepts
5. Command on Verbal and Written communication skills.
6. Team player
   Additional Information :
   Work Location – Pune
   Qualification – M.Pharm / B.Pharm / BAMS / BHMS / Pharm.D / BDS
   Experience – Minimum 0.4 – 2 Years in PV.
   End Date : 25th July, 2023

Send resumes to archita.majumdar@wipro.com