Associate Director, Global Scientific Content
Madrigal Pharmaceuticals
Summary
Willingness to travel up to 30% for conferences, various corporate locations, and stakeholder meetings, including overnight trips
Job description
Key Responsibilities and Primary Activities
Content Development
- Create, adapt, and distribute content across multiple channels to deliver consistent and impactful information for scientific exchange
- Assist in the development of comprehensive content strategies that leverage digital and omnichannel approaches to enhance engagement with healthcare professionals (HCPs) and internal stakeholders, ensuring alignment with scientific communication platform within compliance and practice standards
- Determine scientific accuracy, stakeholder relevance, and appropriateness of the various formats utilized across all the scientific content materials
- Obtain timely feedback and approval to make adjustment to scientific content materials
- Uphold unwavering commitment to scientific rigor and data-driven decision-making
Cross-functional Collaboration
- Partner closely with colleagues within Scientific Communications, Content and Training including the Training managers
- Partner with internal cross-functional and regional teams to align content priorities
- Collaborate with external vendors and partners as needed to support deliverables
- Contribute to launch readiness and support lifecycle medical affairs activities in alignment with strategic objectives
Strategic Planning and Alignment
- Support the identification and prioritization of scientific content needs of internal and external stakeholders, including Health Systems content, as appropriate
- Ensure content planning is aligned with Madrigal Medical Affairs strategies and Scientific Communication platforms
Congress & External Engagement
- Contribute to U.S. and global medical congress activities, as needed, including support for scientific content and training
Compliance & Quality
- Ensure compliance with regulatory and industry standards, Madrigal policies, ethical guidelines, and proper utilization of the escalation process
- Uphold the highest ethical standards in all external engagements
Travel Requirement
Willingness to travel up to 30% for conferences, various corporate locations, and stakeholder meetings, including overnight trips
Required Qualifications, Skills & Experience
- Advanced degree in a scientific or healthcare discipline (BSc, MD, PharmD, PhD, DNP, etc.)
- Rich scientific background capabilities derived from experience or clinical practice
- A minimum of 3 years headquarters work and/or Scientific Content experience
- Proven ability to understand, communicate, and translate complex scientific information
- Knowledge of Scientific Content and Communication trends and landscape
- Demonstrated ability to plan, lead and create scientific content
- Emphasis on providing leadership though factual evidence gathering influencing and inspiring cross-functional teams to drive innovation and achieve goals
- Ability to interact and strategize with leadership and stakeholders across the business
- Strong knowledge of US/EU healthcare systems, global regulatory standards (e.g., FDA, CE), and medical affairs compliance standards
- Proficiency in Microsoft Office Suite, virtual communication platforms (e.g., Zoom), and CRM systems (e.g., Veeva)
Preferred Attributes
- In-depth knowledge of liver disease; experience in cardiometabolic health or metabolic dysfunction–associated steatohepatitis (MASH)
- Adaptable and proactive in a fast-paced, evolving environment
Requirements
- Advanced degree in a scientific or healthcare discipline (BSc, MD, PharmD, PhD, DNP, etc.)
- Rich scientific background capabilities derived from experience or clinical practice
- A minimum of 3 years headquarters work and/or Scientific Content experience
- Proven ability to understand, communicate, and translate complex scientific information
- Knowledge of Scientific Content and Communication trends and landscape
- Demonstrated ability to plan, lead and create scientific content
- Emphasis on providing leadership though factual evidence gathering influencing and inspiring cross-functional teams to drive innovation and achieve goals
- Ability to interact and strategize with leadership and stakeholders across the business
- Strong knowledge of US/EU healthcare systems, global regulatory standards (e.g., FDA, CE), and medical affairs compliance standards
- Proficiency in Microsoft Office Suite, virtual communication platforms (e.g., Zoom), and CRM systems (e.g., Veeva)
Benefits
- Flexible paid time off
- Medical, dental & vision insurance
- Life/disability insurance
- 401(k) with employer match
- Equity
- Mental health benefits
- Employee assistance program
- Supplemental life insurance
- Legal services
Company overview
Madrigal Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company focused on developing novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), formerly known as non-alcoholic steatohepatitis (NASH), a serious form of fatty liver disease. The company's lead product, Rezdiffra (resmetirom), is a once-daily, oral thyroid hormone receptor (THR)-β selective agonist that targets key underlying causes of MASH in the liver. Rezdiffra received FDA approval in 2024 as the first treatment for MASH with moderate to advanced liver fibrosis, representing a significant breakthrough in hepatology. Headquartered in Conshohocken, Pennsylvania, Madrigal is publicly traded on NASDAQ under the symbol MDGL. The company continues to advance its clinical development programs, including ongoing Phase 3 trials evaluating Rezdiffra for the treatment of compensated MASH cirrhosis. Madrigal's innovative approach addresses a critical unmet medical need in liver disease therapeutics.