Address
Form of work• Bachelor or Master's degree in a scientific, business, or related healthcare area (or closely related discipline, such as health administration or biological sciences)
Experience | Knowledge | Skills
Required
• 5 (five) years in clinical/observational research within pharmaceutical industry, or equivalent
• Work independently and as a Team member with Integrity | Precision | Accomplishment | Motivational Ambition | Respect
• Lead and manage working teams without formal reporting structure
• Strong project management and prioritization skills with demonstrated ability to deliver on operational objectives for complex projects, portfolio planning and project management
• Highly motivated, able to work independently and collaboratively, raising issues with recommendations for solutions
• Principled written and verbal communications, interpersonal skills and ability to collaborate with and influence a wide variety of stakeholders, with a capacity to work across cultures and hierarchical boundaries
• Strong business acumen with ability to determine compliant path forward for new ideas and value-added solutions
Preferred
• PMP or CAPM certification
• Basic knowledge of epidemiologic or outcomes research and statistics
• Knowledge of the Medical Affairs and market access landscape within oncology
• Knowledge of Health Technology Assessment environment
• Collaborate across functional areas and geographic boundaries
Additional: Pharma or Biotech industry background. This is not an IT Project Management role. Hybrid role - 3 days onsite required each week. Site location: Rahway, NJ or Upper Gwynedd PA.
Responsibilities:
Value Medical Project Manager – Lead Project Manager
We are seeking a growth and improvement minded Value Medical Project Manager Lead Project Manager (VMPM) that can help drive our Strategic Operating Priorities. The Value Medical Project Manager Lead Project Manager will advance the development, planning, and execution of the integrated Value and Implementation Plan (V&I) to enable patient access. This role works closely with global cross-functional leads in different business groups within our Company Research Labs and Human Health to ensure the seamless development, coordination, and execution of all aspects of the V&I Plan. This includes aggregation and reporting of internal and external collected insights, tracking of evidence generating activities, planning and operations work for reimbursement/Health Technology Assessment (HTA) submissions / resubmissions and communication of data across different stakeholder groups to inform patient care. The Lead PM plays a critical role to collaborate with the value evidence generating (VT or Value Teams), Medical Affairs (MT or Medical Teams) and cross functional V&I Teams to manage deliverables related to insights, evidence, and communication as part of the V&I plan.
Additional Key Responsibilities
Planning | Prioritization
• Contribute strategic insights to drive operational excellence in the development and tactical execution of V&I plans
• Align and prioritize plans through cross-functional collaboration with key global and regional stakeholders in other groups
• Lead the coordination and execution of launch planning activities e.g., country surveys and strategic workshops
• Coordinate the planning, tracking and delivery of key components of the reimbursement/HTA submission dossiers. Support the preparation for Health Technology Assessment consultations in collaboration with local affiliates and the cross functional team
Communications Management
• Lead planning efforts related to internal global/regional team meetings including agendas, decisions, action items
• Manage document repositories and systems used for the exchange of information with affiliates and internal/external collaborators
• Coordinate and facilitate interactions and communications with countries and ensure that key learnings are shared across markets and therapeutic areas; facilitate communication with alliance partners
• Manage the V&I book of business (including Non-Interventional Studies, MISP, publications, etc.)
Stakeholder Management
• Collaborate with internal teams on the planning of deliverables related to scientific expert input and related activities; collaborate with alliance partners
• Lead the planning and preparation for key product development stage gate interactions with our Research & Development Division and Human Health senior leadership
• Coordinate medically important activities requiring therapeutic area coordination, including Regional and Local Data Generation study planning cycle
Reporting | Tracking
• Establish and track key performance indicators and value metrics for the global & regional plans and reimbursement/ Health Technology Assessment submission plans
• Provide financial stewardship, and milestone tracking of V&I Plan aligned global/regional activities and projects
Risk Management
• Manage Risk, Actions, Decisions, and Issues for the Value Evidence Generating, Medical Affairs and cross functional V&I Teams
• Support internal and department processes and procedures, including global and local compliance, to ensure compliant execution of team's activities and projects
• Collaborate extensively and troubleshoot issues by providing potential resolutions when necessary with internal and external partners to ensure timely management and dissemination of V&I deliverables and reimbursement/HTA dossier components
If interested ; kindly get back with answers:
1-how many years of exp epidemiologic or outcomes research and statistics
2-How many years of exp in Running and Managing clinical/observational research within pharmaceutical industry, or equivalent
3-Are you PMP or CAPM certification
4-How many years of exp in the Medical Affairs and market access landscape within oncology
5-Which location you wants to work from Rahway NJ or North Wales PA address as undeR:
351 North Sumneytown Pike, North Wales, PA
126 E. Lincoln Avenue, Rahway, NJ 07065
