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MSD एक वैश्विक बायोफार्मास्युटिकल कंपनी है, जो कैंसर, संक्रामक रोगों, हृदय एवं चयापचय संबंधी स्थितियों और रोकथाम-केंद्रित देखभाल जैसी प्रमुख स्वास्थ्य चुनौतियों के लिए दवाइयों और टीकों को आगे बढ़ा रही है। संयुक्त राज्य अमेरिका, कनाडा और प्यूर्टो रिको में Merck & Co., Inc. के नाम से जानी जाने वाली MSD वैज्ञानिक अनुसंधान को विकास और वाणिज्यिक विशेषज्ञता के साथ जोड़कर लोगों और पशुओं तक स्वास्थ्य सेवाओं से जुड़े समाधान पहुँचाती है।
इसका कार्य मानव स्वास्थ्य, पशु स्वास्थ्य तथा अनुसंधान एवं विकास के क्षेत्रों में फैला हुआ है, जिससे वैज्ञानिक, क्लिनिकल, वाणिज्यिक, परिचालन और कॉर्पोरेट टीमों में पेशेवरों के लिए अवसर बनते हैं। दुनिया भर के विभिन्न क्षेत्रों में अपनी गतिविधियों के साथ, MSD का करियर-केंद्रित कार्य अनुसंधान, सहयोग, समावेशन और वैश्विक स्वास्थ्य में जिम्मेदार प्रगति पर इसके ध्यान को दर्शाता है।
Director, Global Scientific and Value Content – Payor
Lead global scientific and value content strategy for payor medical affairs at MSD. Oversee scientific planning, payer-focused content, cross-functional programs, analysis, and team development.
संयुक्त राज्य
न्यू जर्सी
पेंसिल्वेनिया$1,90,800 – $3,00,300 / वर्ष
हाइब्रिडपूर्णकालिकलीडआवश्यक भाषा: अंग्रेज़ीकंटेंट मार्केटिंग मैनेजरविवरण
- Define and guide V&I Plans and the Scientific Platform
- Develop, prioritize, and deliver annual GSVC product plans aligned with V&I Plans and the Scientific Platform
- Engage stakeholders and integrate medical insights into product planning
- Direct the development, review, approval, and communication of GSVC content
- Create or delegate medical information letters, FAQs, disease and product slide decks, congress booth materials, and digital medical content
- Evaluate materials for scientific accuracy, relevance, appropriate literature, internal information, and company standards
- Coordinate stakeholder input for content development, review, and approval, including CRT prioritization and reviewed-content management for the Payor team
- Communicate approved materials to Medical Information and Global Medical and Scientific Affairs stakeholders
- Develop globally reusable materials with Outcomes Research and address payer-landscape requirements
- Act as a subject-matter expert and lead complex product projects and initiatives
- Mentor and support GSVC P3/P4 staff and newly hired V&I GMVC team members
- Lead internal training on GSVC disease and product content
- Collaborate globally with Publications, Medical Directors, Payor and Health System Medical Affairs, Compliance, PDT, Outcomes Research, MSLs, and other stakeholders
- Direct complex cross-functional initiatives and departmental process improvements
- Write and maintain SOPs and lead organizational or cross-organizational initiatives
- Coordinate coverage and contribute as a medical writer for Global Input Meetings
- Provide strategic direction on complex issues, escalations, regulatory and compliance matters, and team objectives
- Perform quantitative and qualitative analyses and communicate findings
- Lead onboarding and training for core functions
- Promote change, innovation, and cross-functional collaboration
आवश्यकताएँ
- MD, PharmD, or PhD with at least five years of relevant Medical Affairs experience; or MSN, BS in Pharmacy, or MS in Life Sciences with at least 10 years of relevant Medical Affairs experience; or BS in Nursing or Life Sciences with at least 15 years of relevant Medical Affairs experience
- Deep knowledge of healthcare systems and payer processes and environments
- Relevant pharmaceutical-industry experience in Medical Affairs or Outcomes Research
- Demonstrated leadership through initiatives, mentoring, process improvement, and innovation
- Excellent scientific writing and verbal communication skills
- Ability to build networks, set priorities, and collaborate across functions
- Strong organizational and prioritization abilities
- Effective multitasking and problem-solving skills
- Advanced degree preferred
- Experience with global health systems and expertise in payer organizations
- Experience leading multiple global or regional Medical or Scientific Affairs Plans
- Experience with promotional review or medical and legal review processes
- Ability to create or present scientific content for scientific exchange with external customers
- Ability to negotiate with cross-functional teams
- Experience working across geographies with varying regulatory and compliance requirements
- Broad knowledge spanning multiple related therapeutic areas
- Strong analytical capability with the ability to turn strategy into action plans
- Established mentoring experience
- Ability to work effectively in a complex, global, team-based organization
- Visa sponsorship is not available
- Must reside in the United States or Puerto Rico
लाभ
- Annual bonus
- Long-term incentive, where applicable
- Medical, dental, and vision coverage
- Additional insurance benefits for employees and families
- Retirement benefits, including a 401(k) plan
- Paid holidays
- Vacation leave
- Compassionate leave
- Sick leave
- Hybrid work arrangement
- 10% travel
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