This position provides regional regulatory strategic implementation support for products in one or more therapeutic areas, collaborating with global and regional leaders to execute regulatory strategies.
Locations (4)
Horsham, Pennsylvania, United States
Raritan, New Jersey, United States
Spring House, Pennsylvania, United States
Titusville, New Jersey, United States
Compensation
The anticipated base range for this position is $120,000.00 - $207,000.00
Responsibilities
Implementing the regional regulatory strategy, including regulatory submission plans.
Representing the regions and contributing to regional & global regulatory strategy through product-related teams.
Advising product teams regarding regional and local requirements and impact of supply chain decisions.
Leading Regional Working groups to ensure timely execution of product objectives.
Facilitating tactical implementation at the regional level and ensuring effective communications.
Requirements
Bachelor's degree with 8 years experience (5 years pharm regulatory)
Masters/PharmD with 6 years experience (4 years pharm regulatory)
PhD with 4 years experience (3 years pharm regulatory)
Lead development and dissemination of evidence-based scientific materials for payer and health system audiences, support AI-generated content accuracy, and drive metrics and customer insights.
Compensation
The anticipated base pay range for this position is : $120,000.00 - $207,000.00
Responsibilities
Lead development and timely dissemination of tailored, evidence-based scientific materials for assigned therapeutic area products
Support development of AMCP standard and pre-approval dossiers, Medicaid formulary requests, and custom requests
Engage in shaping and development of the Payer Digital Assets in collaboration with Med Info CSI-Digital partners
Guide creation and delivery of responses to unsolicited Medical Information Requests from Payers and Health Systems
Support development and dissemination of scientific information in support of assigned products to Clinical Decision Resource Organizations
This role is responsible for the development and execution of Global Supply Management strategic sourcing strategies in support of the Technology (Research and Development) community. The primary purpose is to identify cost-effective solutions, drive value creation, and foster supplier partnerships.
Compensation
The range for this position is $129,903.00 - $178,617.00 assuming full time status.
Responsibilities
Leads the development, communication, and execution of GSM Strategic Sourcing strategies and plans to procure products or services
Develop and execute comprehensive strategic sourcing strategies for Research and Development
Conduct detailed spend analysis to identify opportunities for increased spend under contract, ensuring cost optimization and supplier consolidation
Works with Business, GSSM, and Buyers on assigned global commodities to prepare and solicit competitive bids, quotations, and proposals
Lead and manage a small team of procurement professionals, providing guidance, mentorship, and support
Requirements
Bachelor of Science Degree in Supply Chain Management
Support profitable growth and operational excellence by combining pricing analysis, offer validation support, performance reporting and process improvement.
Design and deliver end-to-end learning solutions across the organization for multiple business verticals in Global Capability Network to build leadership and behavioural capabilities.
Responsibilities
Design and deliver end-to-end learning solutions that build leadership and behavioural capabilities
Partner with business leadership, HR and global functions to define and implement sustainable learning initiatives
Lead data analysis to build advanced understanding of learning consumption and measurable impact
Track learner compliance with mandatory and recommended learning requirements including onboarding training
Use learning measurement and analytics to assess efficiency and effectiveness
The Global Medical Alliance Lead is responsible for leading the medical relationship with assigned strategic partners and ensuring alignment of Medical Affairs activities across Medison's markets. The role serves as the primary medical point of contact for partner organizations and works in close collaboration with the Commercial Alliance Lead and cross-functional Alliance Teams.
Responsibilities
Serves as the primary medical point of contact for alliance partners, ensuring effective medical collaboration and strategic alignment between partner organizations and Medison.
Represents Global Medical Affairs in cross-functional Alliance Team meetings and governance forums, as required.
Leads the medical strategy from launch preparation through launch and across the full product lifecycle, ensuring continuous adaptation to evolving evidence, stakeholder needs, and market dynamics.
Collaborates cross-functionally to develop and execute Global Medical Affairs strategies and activities for assets within the assigned Therapeutic Area.
Drives alignment on medical strategy, scientific content, and key messaging across functions and regions to ensure a consistent and scientifically robust approach.
Requirements
Advanced Degree in life sciences such as M.D, PhD or PharmD or DVM
Nice to have: M.D with specialty and experience in the field of cardiology
We are looking for an Associate Project Manager to own defined workstreams or smaller projects within Global Business Services (GBS) transformation programmes.
Responsibilities
Own agreed deliverables and outcomes for defined workstreams or smaller projects within delegated scope, cost, time and quality limits.
Own and maintain project plans for assigned projects or workstreams.
Monitor delivery against agreed limits. Resolve issues and take corrective action, escalating exceptions and proposed changes to the Lead Project Manager.
Coordinate activity across functional specialists, sending teams, delivery centres, the programme office, change teams, and service management teams.
Support transition activity through mobilisation, design, knowledge transfer, readiness, go-live and stabilisation.
Requirements
Working towards a recognised PM qualification such as APM PMQ, PMP or PRINCE2
Lead safety evaluations, data analysis, report writing, and support product safety management teams for cell therapy products.
Locations (3)
Horsham, Pennsylvania, United States
Raritan, New Jersey, United States
Titusville, New Jersey, United States
Compensation
The anticipated base pay range for this position is : $120,000.00 - $207,000.00
Responsibilities
Lead safety evaluations, including strategy discussions, collaborating with stakeholders, data retrieval, data analysis, report writing, and report revision.
Ensure high-quality safety evaluations and reports with minimal-to-moderate comments from stakeholders and minimal-to-moderate revisions required.
Provide support to Associate Director SASs for novel projects without defined processes.
Leading regional working groups to ensure timely execution of product objectives
Facilitating tactical implementation at the regional level and ensuring effective communication
Requirements
Bachelor's degree
Master's/PharmD
PhD
Nice to have: Experience in AP, LA, EMEA countries
Nice to have: knowledge of drug development regulations
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