Overview
On Site
Full Time
Skills
Operational Efficiency
FOCUS
Business Process
System Implementation
IQ
OQ
PQ
Web Portals
Web Development
Optimization
Interfaces
Budget
Stakeholder Engagement
Quality Assurance
Process Optimization
Privacy
Health Care
Pharmaceutics
Waterfall
Regulatory Compliance
Pharmaceutical Industry
Data Integrity
Communication
Leadership
Stakeholder Management
Management
Life Sciences
MBA
Veeva
Customer Relationship Management (CRM)
Documentation
Change Management
Data Analysis
Reporting
Decision-making
Project Management
PMP
Agile
GxP
Collaboration
Job Details
Job Description
We are seeking a dynamic and experienced Medical Affairs Business Implementation Lead to drive the execution of strategic initiatives, with a focus on digital transformation projects and validated systems. This role serves as a critical liaison between Medical Affairs business units and IT, ensuring seamless integration of technology solutions, including GxP-compliant systems, to enhance operational efficiency and support healthcare professionals (HCPs). The ideal candidate will bring expertise in Medical Affairs, project management, and digital tools to deliver innovative, compliant solutions that align with organizational goals.
Key Responsibilities
Strategic Implementation: Support the planning, execution, and delivery of Medical Affairs projects, with a focus on digital transformation initiatives and validated systems that enhance business processes and HCP engagement.
Cross-Functional Collaboration: Act as the liaison between Medical Affairs business units and IT teams to translate business needs into technical requirements, ensuring alignment on project goals and compliance with GxP standards.
Digital Transformation: Oversee the implementation of digital tools and platforms, including Veeva Vault, VeevaLink, Veeva CRM, Quello, and Sci Max, ensuring integration with GxP systems and adherence to validation requirements.
Validated Systems Implementation: Manage the deployment of GxP-compliant systems, ensuring proper validation processes (e.g., IQ/OQ/PQ) and compliance with regulatory standards.
Portal and Website Development: Drive the creation and optimization of portals and websites tailored for HCPs, ensuring user-friendly interfaces, regulatory compliance, and integration with validated systems.
Project Management: Develop and manage project plans, timelines, budgets, and resources to ensure on-time, high-quality delivery of initiatives, including those involving validated systems.
Stakeholder Engagement: Collaborate with internal stakeholders (e.g., Medical Affairs, IT, Quality Assurance, Compliance, and Commercial teams) and external partners to align on project objectives and deliverables.
Process Optimization: Identify opportunities to improve Medical Affairs processes through technology, data analytics, and validated systems.
Compliance and Quality: Ensure all initiatives, including GxP systems, adhere to regulatory, compliance, and data privacy requirements within the pharmaceutical and healthcare industry.
Qualifications
Experience:
6-10 years of experience in Medical Affairs and project management within the pharmaceutical or biotech industry.
Proven track record in leading digital transformation projects, with hands-on experience implementing tools such as Veeva Vault, VeevaLink, Veeva CRM, Quello, or Sci Max.
Demonstrated experience working with GxP systems and implementing validated systems, including knowledge of validation processes and regulatory requirements
Experience in developing or managing portals and websites for HCPs is highly desirable.
Skills:
Strong understanding of Medical Affairs operations and the ability to bridge communication between business units and IT.
Expertise in implementing and managing GxP-compliant systems, ensuring validation and regulatory compliance.
Exceptional project management skills, with proficiency in methodologies such as Agile or Waterfall.
Familiarity with regulatory and compliance requirements in the pharmaceutical industry, including GxP and data integrity standards.
Excellent communication, leadership, and stakeholder management skills.
Ability to manage multiple projects simultaneously in a fast-paced environment.
Education:
Bachelor's degree in Life Sciences, Business, or a related field; advanced degree (e.g., MBA, MS, or PharmD) preferred.
Technical Expertise:
Hands-on experience with Medical Affairs platforms (e.g., Veeva Vault, VeevaLink, Veeva CRM, Quello, Sci Max) is strongly preferred.
Knowledge of digital tools for medical inquiry response and HCP engagement platforms.
Experience with GxP system validation processes and documentation.
Preferred Qualifications
Experience with change management and driving adoption of new technologies, including validated systems, within Medical Affairs teams.
Familiarity with data analytics and reporting tools to support decision-making in a GxP environment.
Certification in project management (e.g., PMP, Agile, or equivalent) or GxP-related certifications is a plus.
Why Join Us?
Opportunity to lead cutting-edge digital transformation projects and validated system implementations in a high-impact role.
Collaborate with cross-functional teams in a dynamic, innovative environment.
Contribute to improving HCP engagement and advancing patient outcomes through compliant, technology-driven solutions.
#RecruitPS
We are seeking a dynamic and experienced Medical Affairs Business Implementation Lead to drive the execution of strategic initiatives, with a focus on digital transformation projects and validated systems. This role serves as a critical liaison between Medical Affairs business units and IT, ensuring seamless integration of technology solutions, including GxP-compliant systems, to enhance operational efficiency and support healthcare professionals (HCPs). The ideal candidate will bring expertise in Medical Affairs, project management, and digital tools to deliver innovative, compliant solutions that align with organizational goals.
Key Responsibilities
Strategic Implementation: Support the planning, execution, and delivery of Medical Affairs projects, with a focus on digital transformation initiatives and validated systems that enhance business processes and HCP engagement.
Cross-Functional Collaboration: Act as the liaison between Medical Affairs business units and IT teams to translate business needs into technical requirements, ensuring alignment on project goals and compliance with GxP standards.
Digital Transformation: Oversee the implementation of digital tools and platforms, including Veeva Vault, VeevaLink, Veeva CRM, Quello, and Sci Max, ensuring integration with GxP systems and adherence to validation requirements.
Validated Systems Implementation: Manage the deployment of GxP-compliant systems, ensuring proper validation processes (e.g., IQ/OQ/PQ) and compliance with regulatory standards.
Portal and Website Development: Drive the creation and optimization of portals and websites tailored for HCPs, ensuring user-friendly interfaces, regulatory compliance, and integration with validated systems.
Project Management: Develop and manage project plans, timelines, budgets, and resources to ensure on-time, high-quality delivery of initiatives, including those involving validated systems.
Stakeholder Engagement: Collaborate with internal stakeholders (e.g., Medical Affairs, IT, Quality Assurance, Compliance, and Commercial teams) and external partners to align on project objectives and deliverables.
Process Optimization: Identify opportunities to improve Medical Affairs processes through technology, data analytics, and validated systems.
Compliance and Quality: Ensure all initiatives, including GxP systems, adhere to regulatory, compliance, and data privacy requirements within the pharmaceutical and healthcare industry.
Qualifications
Experience:
6-10 years of experience in Medical Affairs and project management within the pharmaceutical or biotech industry.
Proven track record in leading digital transformation projects, with hands-on experience implementing tools such as Veeva Vault, VeevaLink, Veeva CRM, Quello, or Sci Max.
Demonstrated experience working with GxP systems and implementing validated systems, including knowledge of validation processes and regulatory requirements
Experience in developing or managing portals and websites for HCPs is highly desirable.
Skills:
Strong understanding of Medical Affairs operations and the ability to bridge communication between business units and IT.
Expertise in implementing and managing GxP-compliant systems, ensuring validation and regulatory compliance.
Exceptional project management skills, with proficiency in methodologies such as Agile or Waterfall.
Familiarity with regulatory and compliance requirements in the pharmaceutical industry, including GxP and data integrity standards.
Excellent communication, leadership, and stakeholder management skills.
Ability to manage multiple projects simultaneously in a fast-paced environment.
Education:
Bachelor's degree in Life Sciences, Business, or a related field; advanced degree (e.g., MBA, MS, or PharmD) preferred.
Technical Expertise:
Hands-on experience with Medical Affairs platforms (e.g., Veeva Vault, VeevaLink, Veeva CRM, Quello, Sci Max) is strongly preferred.
Knowledge of digital tools for medical inquiry response and HCP engagement platforms.
Experience with GxP system validation processes and documentation.
Preferred Qualifications
Experience with change management and driving adoption of new technologies, including validated systems, within Medical Affairs teams.
Familiarity with data analytics and reporting tools to support decision-making in a GxP environment.
Certification in project management (e.g., PMP, Agile, or equivalent) or GxP-related certifications is a plus.
Why Join Us?
Opportunity to lead cutting-edge digital transformation projects and validated system implementations in a high-impact role.
Collaborate with cross-functional teams in a dynamic, innovative environment.
Contribute to improving HCP engagement and advancing patient outcomes through compliant, technology-driven solutions.
#RecruitPS
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