Podsumowanie roli od JobGrid
Associate Product Manager (Commercial) at Clinigen: Warriewood, Australia; Na miejscu; Marketing i wzrost. This listing is part of JobGrid's Oferty pracy dla product managerów z publicznych stron firm. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.
- Location and workplace: Warriewood, Australia, Na miejscu
- Role classification: Marketing i wzrost
- Source freshness: checked by JobGrid on 2026-05-28.
- Application path: candidates continue to the employer application page with non-personal referral tags.
Clinigen is a leading global specialty pharmaceutical and services company dedicated to improving patient outcomes through the secure and timely delivery of vital medicines worldwide. With over 1,100 employees and operations spanning the UK, US, EU, JAPAC, and South Africa, Clinigen continues to experience significant growth and innovation in the pharmaceutical sector.
Position Overview
The Associate Product Manager supports the execution of brand strategy and tactical marketing initiatives, working cross‑functionally to deliver commercial objectives while ensuring compliance with local pharmaceutical regulations.
Key Responsibilities
Brand Strategy & Execution
• Support the Senior Marketing Manager in executing strategy and annual brand plans
• Assist in the development of a tactical marketing initiatives aligned with brand positioning and business objectives.
• Contribute to product lifecycle management activities (launch, growth, maturity)
• Monitor key financial areas including the recording of monthly sales, expenditure and margins
• Cooperation with implementation of activities with key customers
• Attend relevant trade events
Marketing and Promotional Activities
• Develop and coordinate promotional materials for healthcare professionals, including detailing aids, visual aids, digital assets, and conference materials
• Coordinate with agencies (creative, media, digital) for asset development.
• Manage marketing campaigns across channels (sales force, digital, conferences, medical education)
• Track campaign effectiveness and recommend optimizations.
• Manage approval process through Veeva PromoMats with approval team and agency to meet agreed timelines
• Distribution of marketing materials to the sales team, conference venues and customers as required
• Manage Sales and Marketing SharePoint and ensure approved marketing materials assets are filed.
• Keep inventory of marketing materials up to date in the marketing stock room. Discard expired items.
CRM/IQVIA Reporting and Data Management
• Coordinate with Operations to ensure Monthly ex-factory data submitted to IQVIA
• Provide troubleshooting support on IQVIA and Veeva to the sales and marketing teams.
• Liaising with Veeva and IQVIA for new updates/ changes
• Provide Veeva CRM training to new staff as required
• Submit PBS pricing disclosure data every cycle on PDDA portal with information from Finance and Operations.
Budget Management and Reporting
• Enter new vendor on Navex system
• Assist in preparing SOW and coordinate MSA approval with management
• Initiate and escalate payment SOP on supplier invoices
• Responsible for monitoring spend to budget
Commercial Support
• Manage conferences, meetings & events
• Provide support for commercial team meetings (arrange meetings, agenda and minutes)
• Complete required reports within designated timeframes (e.g. monthly reports, expenses)
• Ensure filing and documentation is up-to-date and in compliant with standard processes and formats
Collaboration and Teamwork
• Build effective cross‑functional relationships with Supply Chain, Finance, Medical, Regulatory, Quality, and Customer Service.
• Communicate effectively with internal teams and management.
• Support efficient execution of projects and initiatives.
Knowledge and Compliance
• Ensure all activities comply with Medicines Australia Code and local regulations.
• Maintain knowledge of products, competitors, and therapeutic areas.
• Always follow pharmacovigilance and internal SOPs.
• Participate in relevant industry and product education activities.