Sr. Program Lead, Process Optimization (PS Content Optimization)

About This Role

We are seeking a skilled Sr. Program Lead, Process Optimization to implement regulatory, legal, and commercial compliance controls for identified areas of promotional risk. This position is responsible for working cross-functionally to develop and maintain Patient Services documentation and the Knowledge Management system to store documentation, including Patient Services policies, talking points, departmental procedures, frequently asked questions, scripts, letters, and related materials. This role helps provide consistent guidance for Patient Services business practices while supporting compliant, customer-focused communications.

Who We Are

Patient Services partners across commercial, medical, legal, regulatory, compliance, quality, training, operations, and technology teams to support business practices that are clear, consistent, compliant, and centered on the customer experience. The team develops and maintains documentation, processes, and knowledge management resources that guide frontline agents, program teams, Operations Leadership, and cross-functional partners.

What You’ll Do

Patient Services Material Development and Oversight

• Collaborate with US Business teams, including marketing, medical, legal, regulatory, and related partners, to develop communication strategies and materials for Patient Services customer written and verbal interactions, including talking points, letters, emails, faxes, and training materials.
• Determine what information Patient Services can share with customers; create talking points and scripts to support discussions; and provide direction and oversight to Operations Leadership on when and how materials should be used.
• Implement and manage the cross-functional document review process, including process steps, roles and responsibilities, communication, escalation paths, and continuous improvement to ensure documents are updated according to defined requirements.

Departmental Knowledge Management

• Create and maintain departmental practices, scripts, frequently asked questions, and letters containing promotional language for the Patient Services department, ensuring alignment with brand strategy and legal and regulatory requirements.
• Identify opportunities to improve content in support of business and customer needs; research market trends and developments in knowledge management technology, templates, and document management; and recommend alternative solutions.
• Manage the Patient Services departmental knowledge management structure and system.
• Identify and resolve system issues, partnering with IT Business Analysts and programmers on ongoing system development to improve organizational and program performance.
• Manage program KPIs and report results on a quarterly basis.

Promotional Guardrails and Customer Experience Oversight

• Support implementation of promotional guardrails by creating and implementing policies and documentation that apply to Patient Services, as determined by US Commercial Legal, Regulatory, Marketing, Commercial, and Promotional Compliance teams.
• Work with Operations Leadership to determine communication and training needs associated with new policies and procedures, creating materials as needed.
• Identify impacts of process or language on the customer experience and recommend solutions that reflect excellence from the customer perspective.
• Create forums to understand the customer experience and identify opportunities for improvement; work with appropriate groups to implement improvements.
• Partner with Quality and Training to help ensure promotional guardrails and the customer experience are optimized.

Promotional Review Committee

• Manage submissions and represent Patient Services at the cross-departmental Promotional Review Committee for two to four BIIB products.
• Partner with medical, legal, regulatory, drug safety, and marketing representatives to ensure record approval.
• Use strong knowledge of Patient Services business needs to explain requirements and influence PRC members so content remains user- and customer-friendly while aligned with legal and regulatory requirements.
• Collaborate with legal, regulatory, drug safety, and marketing representatives to review new content, new concepts, or significant changes to existing content and ensure alignment with each group’s requirements.

Who You Are

You are a collaborative, detail-oriented professional who can translate complex compliance, regulatory, legal, and operational requirements into clear, practical guidance for Patient Services teams. You are comfortable influencing without authority, facilitating cross-functional alignment, and balancing business needs, customer experience, and promotional compliance requirements. You bring strong technical writing skills, sound judgment, and the ability to prioritize quickly in a dynamic environment.

Required Qualifications

• Bachelor’s degree required.
• 3–5 years of experience within Patient Services or the Patient Support industry.
• Technical writing ability, including the ability to write and edit for clarity, conciseness, and accuracy.
• Ability to produce clear and concise written and verbal communications for a wide range of audiences, including frontline agents, program teams, Operations Leadership, and Biogen Compliance.
• Ability to influence and facilitate effective outcomes without authority.
• Strong sense of prioritization and ability to shift priorities quickly to meet business needs.
• Ability to identify issues and partner with others to identify, implement, communicate, and train on solutions.
• Strong collaboration and interpersonal skills.
• Ability to understand and navigate Visio diagrams and translate them into logically written steps.
• Demonstrated critical and creative thinking, problem-solving skills, and sound judgment.
• Experience using AI-enabled tools to support content development, drafting, editing, knowledge management, or process documentation in a compliant and business-appropriate manner a plus

 

Job Level: Professional

Additional Information

The base compensation range for this role is: $81,000.00-$105,000.00

Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. 

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:

• Medical, Dental, Vision, & Life insurances
• Fitness & Wellness programs including a fitness reimbursement 
• Short- and Long-Term Disability insurance
• A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
• Up to 12 company paid holidays + 3 paid days off for Personal Significance 
• 80 hours of sick time per calendar year
• Paid Maternity and Parental Leave benefit 
• 401(k) program participation with company matched contributions
• Employee stock purchase plan 
• Tuition reimbursement of up to $10,000 per calendar year 
• Employee Resource Groups participation

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.