Project Manager (Medical Affairs )
Apply NowCompany: Intelliswift
Location: Rahway, NJ 07065
Description:
Job ID: 24-04095
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.
Qualifications:
Education Required:
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 Skills / Experience:
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
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
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.
Qualifications:
Education Required:
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 Skills / Experience:
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
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