Job Title

Location: Hyderabad;Role OverviewThe Project Manager will own endtoend delivery of creative, content, and digital initiatives in a regulated pharmaceutical environment, acting as the single orchestration point between brand stakeholders and internal delivery teams.Key ResponsibilitiesDrive delivery from intake and planning through execution, MLR/LMR review, approval, and releaseOrchestrate crossfunctional teams across creative, content, UX/UI, web, and digital productionManage MLR/LMR workflows, version control, audit trails, and compliance documentationAct as the primary interface between brand, medical, legal, regulatory, agencies, and delivery teamsOwn scope, timelines, resourcing, risks, dependencies, and change controlEnsure assets are onbrand, compliant, highquality, and delivered on timeTrack delivery metrics (cycle time, firstpass approvals, rework, throughput) and drive continuous improvementRequired Experienceproject management experience, with strong life sciences/pharma exposure and a deep understanding of pharma content lifecycles: claims development, annotations/references, fair balance, labeling-driven changes, expiry/refresh, country adaptation.Experience with scaled delivery models (POD-based structures with a PM per POD).Comfort operating in high-volume, high-urgency environments with shifting priorities and tight deadlines.Proven delivery of creative, content, and digital marketing assets in regulated environmentsHandson experience managing MLR/LMR processes (Veeva or similar workflows preferred)Strong stakeholder management, planning, and execution skillsWork management: Workfront / Jira / Azure DevOps / Smartsheet / MS Project (any comparable)Collaboration: Teams, SharePoint, ConfluenceReview/approval platforms (preferred): Veeva-style workflows and regulated approval systems.Creative and digital collaboration awareness (not hands-on required): Figma/Adobe ecosystem basics, DAM basics.What Success Looks LikePredictable, compliant delivery at scaleFaster review cycles with minimal reworkHigh stakeholder confidence and operational excellenceReporting, Metrics & Operational ExcellenceBuild dashboards and reporting packs:Ontime delivery %, cycle time, firstpass approval rate, rework rate, throughput by asset type, aging in review, and backlog health.Identify systemic bottlenecks (e.g., review latency, unclear briefs, rework drivers) and implement fixes.Standardize ways of working with templates, asset checklists, and process handbooks to reduce errors and improve predictability.Therapeutic & Domain Experience (Required)Cardiovascular, Immunology, Oncology (Hematology and Solid Tumors), NeuroscienceExperience supporting labelupdate led revisions across asset families and channelsComfort operating in regulated promotional/nonpromotional content environments and review cyclesDeliverables You Will Own (Typical)Project charter / kickoff pack, resourcing plan, integrated schedule, decision log, action trackerMLR submission package (final files, annotations, references, change summaries) & approval archiveWeekly status reports and leadership readoutsRelease readiness checklist and handover notes to publishing/ops