Role: UK Life (Life & Pension) - customer service Job location: Malad (TRIL) Band: BPO 1/2 Salary Range: up to 7 LPA Requires 1-2 yrs international BPO exp, excellent communication, and CRM skills Required Candidate profile Handle UK life & pension customer queries via phone/email, resolve issues, and ensure compliance. Rotational shifts. Offers training, growth opportunities, and benefits.

Experienced Medical Writer with 5 years in authoring/editing clinical documents including protocols, CSRs, regulatory submissions (US/EU), and eCTD publishing using tools like Docubridge. Skilled in xEVMPD, RIM, and Veeva Vault. Required Candidate profile Strong knowledge of ICH-GCP, CTD format, and various therapeutic areas. Excellent communication, analytical, and coordination skills. Based in Mumbai/Pune/Bangalore with international BPO experience.

Authoring/editing of clinical documents Review of the clinical/safety documents Assist senior writers Keep abreast of project status Maintain and develop current knowledge of regulatory guidelines, technological advances and industry standards Required Candidate profile 3+ years’ of authoring/editing experience in medical writing domain across different therapeutic areas in clinical documents including protocol, informed consent document, clinical study report, etc.

• Respond to queries/ clarifications from EC/ IRBs and on sites • Attend drug safety/external meetings/investigator meetings • Patient eligibility review • Review AE/ SAEs • Protocol training of site staff, CRAs etc

Leads and mentors a team of Clinical Data Reviewer(CDR). Work closely with study team to meet study milestones. Provide inputs to protocol amendments, review and lead post go live changes to the eCRF, as appropriate. Required Candidate profile 5+ Years of Core Clinical Data Management Experience . Study Data Manager Hands on experience in all phases of Clinical Data Management with minimum 1 year of experience of leading a clinical trial.

Regulatory Submissions Publisher – Mumbai/Bengaluru (Night Shift). Prepares & QC’s regulatory dossiers (IND, NDA, CTA, BLA, IMPD, MAA) for US, EU, Canada, ANZ. Handles EDMF, COS/CEP, MRP/DCP/CP filings Required Candidate profile Requires 2+ yrs pharma publishing exp, Documentum/Liquent Insight skills, MS Office proficiency. Must have international BPO exp, grad degree, and be based in Mumbai/Bangalore. No ex-TCS candidates.

We are seeking a Clinical Programmer with expertise in JReview listings, dashboards, and visualizations to support clinical data review, safety monitoring, data validation and clinical data visualization, analysis, and reporting for clinical trials. Required Candidate profile 4+ Years of experience. MS SQL Server and R, R packages e.g., Tidyverse, ggplot2, dplyr, Pipeline creation, or Oracle, SAS, Python, Elluminate, BOXI, Spotfire, Tableau, Macros, RShiny, JReview, Plotly