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Ascendis Pharma

Global Medical Affairs Planning & Effectiveness, Content Platform Lead -Job 2033

princeton, NJ

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Job description

Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.

Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues.

Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.

Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills.

Position Summary

The Global Medical Affairs Planning & Effectiveness, Medical Content Platform Lead is responsible for leading the global operating model, governance framework, and technology strategy for Medical Affairs content management and review processes within Veeva MedComms. This role serves as the business owner for Medical content platforms and capabilities, including Veeva MedComms and related systems, ensuring a scalable, compliant, and efficient framework for content creation, review, approval, distribution, and utilization across global and local markets.

The position requires significant cross-functional leadership and influence across Medical Affairs, Regulatory Affairs, Market Access, Commercial, Legal, Compliance, and Information Technology organizations. The individual will drive strategic alignment, establish governance and decision-making forums, define standards and metrics, lead global change management initiatives, and ensure technology investments support evolving business needs.

In addition, this role provides oversight and strategic direction for medical review processes, driving operational excellence, consistency, compliance, and continuous improvement across content review workflows.

Key Responsibilities

Global Content Governance and Operating Model

Own and evolve the global Medical content governance framework, including policies, standards, taxonomy, metadata strategy, content architecture, and lifecycle management

Establish and maintain an integrated operating model across Medical Affairs, Regulatory Affairs, Market Access, Commercial, and IT to ensure content systems function as a coordinated enterprise capability

Define governance structures, decision rights, prioritization frameworks, and cross-functional steering committees to support effective content operations

Lead resolution of competing stakeholder priorities and drive decisions that balance compliance, usability, scalability, and business objectives

Develop global standards for content repositories while minimizing duplication and ensuring alignment with enterprise architecture principles

Establish and maintain content management best practices and ensure consistent adoption across regions and functions

Platform Ownership and Technology Strategy

Serve as the senior business owner and primary Medical Affairs representative for MedComms and related content management platforms

Partner closely with IT to define platform roadmaps, enhancement priorities, investment strategies, and long-term capability development

Translate business requirements into scalable technical solutions and ensure alignment with Medical Affairs strategic objectives

Lead governance and prioritization of system enhancements, backlog management, taxonomy changes, workflow optimizations, and new capability implementation

Oversee platform adoption, training, user support models, and change management initiatives

Collaborate with vendors and internal technical teams to optimize system performance and user experience

Content Review and Approval Excellence

Provide strategic oversight for medical and non-promotional content review processes globally

Ensure compliant, efficient, and consistent review workflows across cross-functional stakeholders

Establish standards and best practices for content submission, review, approval, documentation, and audit readiness

Oversee review governance forums, prioritization processes, escalation pathways, and decision documentation

Guide support of product launches, new indications, data disclosures, and label updates through effective content review planning

Drive continuous process improvement initiatives to reduce cycle times and enhance review quality

Cross-Functional Leadership

Act as the primary liaison among Medical Affairs, Regulatory Affairs, Market Access, Commercial, Legal, Compliance, and Information Technology

Build strong relationships with senior leaders to align priorities and advance enterprise initiatives

Chair governance committees and facilitate strategic discussions related to content operations and platform capabilities

Influence stakeholders across organizational boundaries without direct authority

Foster collaboration and accountability across global functions and markets

Analytics, Metrics, and Operational Performance

Develop and maintain global performance measurement frameworks for content operations and governance effectiveness

Define key performance indicators related to adoption, utilization, review efficiency, compliance, content accessibility, and operational effectiveness

Create executive dashboards and reporting capabilities that provide visibility into system performance and business outcomes

Monitor trends and identify opportunities for optimization and innovation

Establish market-level targets and benchmarks to support continuous improvement

Change Management and Capability Building

Lead global change management strategies supporting new processes, governance models, and technology initiatives

Develop communication plans, training programs, knowledge resources, and adoption campaigns

Promote awareness and accessibility of available content and platform capabilities

Build organizational capability through education, coaching, and stakeholder engagement

Support development of future-state operating models that enhance effectiveness and scalability across the organization

Requirements

Knowledge, Skills and Experience

Education

Bachelor's degree required

Advanced degree in Life Sciences, Business Administration, Healthcare Management, Information Management, or related field preferred

Experience

Minimum 7 years of progressively responsible experience within the pharmaceutical, biotechnology, or healthcare industry

Significant experience in Medical Affairs operations, content governance, non-promotional review, or regulated content management environments

Demonstrated expertise with Veeva MedComms, Medical content management systems, electronic document management systems, and associated workflows

Experience leading global cross-functional initiatives and governance programs

Proven track record driving business process transformation and technology-enabled operational improvements

Experience partnering effectively with Information Technology organizations and managing enterprise platform strategies

Knowledge and Skills

Strategic leadership and enterprise thinking

Deep understanding of Medical Affairs operations and scientific content workflows

Expertise in content governance, taxonomy, metadata, and repository architecture

Strong knowledge of regulated content review and approval processes

Ability to translate complex business needs into scalable operational and technical solutions

Exceptional influencing and stakeholder management skills

Experience establishing governance structures, decision rights, and prioritization frameworks

Strong business process ownership within highly regulated environments

Excellent communication, facilitation, and executive presentation skills

Strong analytical capability with experience building metrics and performance dashboards

Sound decision-making and judgment in complex organizational situations

Project and change management expertise

Ability to balance consensus-building with decisive leadership

The estimated salary range for this position is $190 - $210K. Actual salary determination is dependent on a variety of factors, some of which include: experience, qualifications, and geographic location. This position may be eligible for a discretionary annual bonus or an incentive compensation plan (eligibility varies based on role and position level), discretionary stock-based long-term incentives, paid time off, and a comprehensive benefits package.

Benefits

401(k) plan with company match

Medical, dental, and vision plans

Company-offered Life and Accidental Death & Dismemberment (AD&D) insurance

Company-provided short and long-term disability benefits

Unique offerings of Pet Insurance and Legal Insurance

Employee Assistance Program

Employee Discounts

Professional Development

Health Saving Account (HSA)

Flexible Spending Accounts

Various incentive compensation plans

Accident, Critical Illness, and Hospital Indemnity Insurance

Mental Health resources

Paid leave benefits for new parents

Ascendis Pharma is proud to be an equal opportunity employer. We are committed to creating an inclusive environment for all employees.

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Worksite address

princeton, NJ, 08543, US

Who can apply

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