Trilogy

Technical Project Manager

• Act as the single point of contact for brand teams working with Indegene on commercial marketing requests
• Work across brands, onsite teams, and offshore delivery teams
• Drive structured collaboration, in-person stakeholder engagement, process oversight, market-level prioritization, and cultural enablement
• Own tactical and technical delivery, converting approved demand into scoped project plans
• Coordinate offshore delivery teams on technical handoffs, QA checkpoints, and dependency tracking
• Represent delivery status, risks, and escalations to client stakeholders
• Serve as liaison among brand leads, channel owners, Activation Leads, and delivery units
• Facilitate country-level campaign planning and localization discussions
• Align stakeholders on customer experience objectives, message relevance, and omnichannel strategy
• Validate brief completeness before production
• Manage and prioritize intake in a high-volume content-factory environment
• Manage multiple concurrent content and campaign workstreams with competing SLAs and priorities
• Use workflow management tools to track timelines, risks, and SLAs
• Validate technical feasibility of briefs and troubleshoot delivery issues
• Ensure QA and channel-specific specifications are complete before delivery
• Maintain production trackers, rate cards, and retainer logs
• Report planned versus actual spend, SLAs, and delivery KPIs
• Contribute to budget reallocation and resource planning decisions
• Provide stakeholders with project status, delivery performance, and operational metrics

Technical Project Manager – Pharma, Agency

Project Manager

• Manage MLR/PRC workflows end-to-end from concept review through final approval, including resubmissions and re-reviews
• Assign and route reviewers based on content type and regulatory requirements
• Manage the material pipeline, including active workflows and offline activities
• Perform readiness assessments using pre-submission checklists to ensure SOP compliance
• Flag non-compliant or incomplete submissions and partner with originators to resolve issues
• Track material expiry and timely re-review or retirement
• Chair PRC/MLR meetings, lead discussions, capture decisions, and log action items
• Prepare and distribute meeting agendas and update them based on reviewer feedback and workflow status
• Attend brand, therapy area, and business-unit prioritization meetings
• Coordinate between reviewers, project owners, agencies, and material owners
• Drive agency accountability for submission quality and process adherence
• Share job aids and policy guidance; identify training gaps and escalate
• Generate compliance reports on submission, review, approval, expiry, and usage status
• Extract and analyze process metrics and provide actionable recommendations
• Maintain therapeutic area trackers and planning and prioritization forecasts
• Run periodic reports, including 90-day re-review and Open Jobs Status reports
• Identify optimization opportunities aligned with business objectives
• Co-create strategies with stakeholders to improve efficiency and measurable impact
• Support process documentation, training materials, and refresher sessions

Project Coordinator – MLR/PRC Promotional Review

Copywriter

• Edit promotional material content for global pharmaceutical clients, checking language, grammar, spelling, punctuation, consistency, and adherence to brand/client guidelines
• Proofread materials to ensure text has not been added or deleted inadvertently
• Ensure MLR reviewer comments are implemented in final compliance copy
• Proofread ISI against the approved version
• Format documents according to journal and congress guidelines
• Ensure adherence to AMA Manual of Style, brand style, and client guidelines
• Consistently deliver high-quality edits exceeding client expectations
• Contribute to knowledge-sharing exercises and resource documentation
• Participate in lead team meetings to discuss complex review resolutions and approaches
• Participate in client calls and collaborate with internal stakeholders for smooth project execution

Copy Editor

• Develop and update content for commercial assets across digital and printed channels
• Create banner ads, emails, sales-representative materials such as i-detail, social media content, websites, posters, slide kits, patient guidelines, sales content, leaflets, and conference materials
• Create promotional communication content for pharmaceutical-industry clients
• Translate science and data into compelling promotional copy while complying with medical, regulatory, legal, and compliance guidelines
• Adapt larger content into smaller, easy-to-read materials while maintaining key medical messaging
• Anchor medical literature references using authentic, current, and up-to-date sources
• Support omnichannel implementation on digital channels
• Participate occasionally in creative projects involving ideation and moving images for campaign-level activity
• Partner with graphic design, brand, and production teams on copy needs, briefs, workshops, and project deliveries
• Follow departmental best practices for processes, communication, project management, documentation, language, grammar, stylization, content search, summarizing, data conflicts, and referencing
• Produce copy drafts to the highest editorial standards
• Participate in client calls as required by projects
• Use, oversee, and harness AI tools to provide accurate and relevant copy content
• Maintain quality, confidentiality, and security while adhering to quality systems, processes, policies, training, and specifications

Technical Project Manager – Pharma, Agency

Project Coordinator – MLR/PRC Promotional Review

Copy Editor

Medical Copywriting Lead