- Страна
- США
- Зарплата
- 213 000 $ – 261 000 $
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Director, Patient Advocacy & Medical Affairs
Исключительная позиция в лидирующей биотехнологической компании с конкурентной зарплатой, бонусами и возможностью работать с передовыми технологиями генного редактирования.
Сложность вакансии
Высокий уровень сложности обусловлен требованием к стажу (более 15 лет) и необходимостью глубокого понимания как научной стороны генного редактирования, так и этических аспектов работы с сообществами пациентов.
Анализ зарплаты
Предложенный диапазон ($213k - $261k) полностью соответствует рыночным стандартам для позиций уровня Director в биотехнологическом хабе Кембриджа (Массачусетс), учитывая узкую специализацию в генной терапии.
Сопроводительное письмо
I am writing to express my strong interest in the Director, Patient Advocacy & Medical Affairs position at Prime Medicine. With over 15 years of experience in the biotechnology sector and a deep-rooted commitment to rare disease communities, I have consistently demonstrated the ability to bridge the gap between complex scientific innovation and the lived experiences of patients. My background aligns perfectly with Prime Medicine’s mission to deliver curative genetic therapies while ensuring the patient voice is integrated into every stage of clinical development.
Throughout my career, I have successfully built long-term, trust-based relationships with global advocacy organizations and led patient advisory boards that directly influenced clinical trial design and endpoint selection. I am particularly drawn to Prime Medicine’s Prime Editing platform and the potential it holds for hematology and immunology. I am confident that my expertise in translating scientific data into patient-centric narratives and my collaborative approach with Medical Affairs and Regulatory teams will contribute significantly to the success of your investigational programs.
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Откликнитесь в primemedicine уже сейчас
Присоединяйтесь к Prime Medicine, чтобы формировать будущее генной терапии, ставя интересы пациентов во главу угла.
Описание вакансии
Company Overview:
Prime Medicine is a leading biotechnology company dedicated to creating and delivering the next generation of gene editing therapies to patients. The Company is leveraging its proprietary Prime Editing platform, a versatile, precise and efficient gene editing technology, to develop a new class of differentiated, one-time, potentially curative genetic therapies. Designed to make only the right edit at the right position within a gene while minimizing unwanted DNA modifications, Prime Editors have the potential to repair almost all types of genetic mutations and work in many different tissues, organs and cell types.
Prime Medicine is currently progressing a diversified portfolio of investigational therapeutic programs organized around our core areas of focus: hematology, immunology & oncology, liver and lung. Across each core area, Prime Medicine is focused initially on a set of high value programs, each targeting a disease with well-understood biology and a clearly defined clinical development and regulatory path, and each expected to provide the foundation for expansion into additional opportunities. For more information, please visit www.primemedicine.com.
Job Title
Director, Patient Advocacy & Medical Affairs
Reports To
VP of Clinical Development
Position Summary
Prime Medicine is seeking an Associate Director or Director, Patient Advocacy & Medical Affairs to lead patient-focused engagement across our rare disease gene-editing programs. This role is central to ensuring that the patient voice meaningfully informs development strategy, clinical trial design, and external engagement, while also supporting Medical Affairs activities with credible, patient-grounded insights.
The successful candidate will build trusted relationships with patient communities, advocacy organizations, caregivers, and clinicians, and will work cross-functionally with Clinical Development, Medical Affairs, Regulatory, and Communications teams. This is a highly collaborative role for a leader who combines deep empathy and credibility with patients and a strong understanding of medical, scientific, and regulatory contexts.
Key Responsibilities
Patient Advocacy Leadership
- Serve as the primary internal advocate for patients and caregivers across rare disease programs.
- Build and maintain long-term, trust-based relationships with:
- Patient advocacy organizations
- Patient leaders and caregivers
- Community groups and foundations
- Ensure patient perspectives are integrated into:
- Clinical trial design and execution
- Endpoint selection and feasibility considerations
- Study materials and participant experience
- Lead patient advisory boards, listening sessions, and community engagements in a compliant and transparent manner, including oversight of sponsorship activities and events as well as inquiry tracking.
- Partner with cross-functional teams to incorporate patient insights into development decisions.
Medical Affairs Partnership & Support
- Collaborate closely with internal teams to:
- Support external scientific engagement with healthcare professionals and key opinion leaders
- Ensure patient-focused insights inform medical strategy and external education
- Contribute to the development and review of:
- Medical and scientific communication materials
- Patient-facing educational resources
- Advocacy-appropriate disease and treatment education content
- Support congress planning, advisory boards and patient panels, and non-promotional medical education activities with a patient-centered lens.
Clinical Development & Cross-Functional Collaboration
- Partner with Clinical Development and Clinical Operations to:
- Provide patient-centric input on protocol design, inclusion/exclusion criteria, and visit burden
- Improve trial awareness, access, and participant experience
- Support regulatory interactions and briefing materials by articulating patient needs and unmet burden.
- Collaborate with Regulatory and Legal teams to ensure advocacy activities are compliant and aligned with company values.
Strategy, Insights & Impact
- Monitor and synthesize patient community insights, unmet needs, and emerging trends across relevant rare diseases.
- Translate patient insights into actionable recommendations for leadership and program teams.
- Help shape long-term patient engagement strategy as programs advance through development.
- Represent the company externally as a credible, compassionate, and scientifically grounded partner to the patient community.
Qualifications
Required
- Bachelor’s degree required; advanced degree (Master’s, PhD, PharmD, MD, MPH) preferred.
- 15+ years of experience in patient advocacy, medical affairs, rare disease engagement, or related roles within biotech, pharma, federal or nonprofit settings.
- Demonstrated experience working directly with patient advocacy organizations and patient communities.
- Strong understanding of clinical development and medical affairs in rare diseases.
- Excellent communication skills, with the ability to translate complex science into patient-appropriate language.
- Proven ability to collaborate cross-functionally in a fast-paced, mission-driven environment.
Preferred
- Experience in gene therapy, gene editing, or other advanced modalities.
- Industry experience supporting early-stage clinical programs.
- Familiarity with regulatory and compliance considerations for patient engagement.
- Background in rare genetic diseases.
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus) and an annual long-term incentive award (e.g., equity).
Prime Medicine offers a comprehensive Total Rewards package with robust health, financial, and wellness benefits—including medical, dental, vision, life insurance, a 401(k) match, and equity programs—along with generous paid time off, wellness days, and company-wide recharge breaks.
Our commitment to employee well-being reflects our belief that when we care for our people, we strengthen our ability to put patients first and make meaningful impact together.
U.S. Pay Range
$213,000—$261,000 USD
Prime Medicine is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, disability, veteran status, or any other classification protected by law.
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Навыки
- Patient Advocacy
- Medical Affairs
- Clinical Development
- Rare Diseases
- Gene Therapy
- Gene Editing
- Stakeholder Management
- Regulatory Compliance
- Scientific Communication
Возможные вопросы на собеседовании
Оценивает способность кандидата влиять на стратегию компании через обратную связь от пациентов.
Приведите пример, когда мнение пациентского сообщества кардинально изменило дизайн клинического исследования или выбор конечных точек. Как вы этого добились?
Важно для понимания того, как кандидат балансирует между наукой и доступностью информации.
Как вы адаптируете сложные научные данные о технологии Prime Editing для аудитории пациентов и их семей, не теряя при этом точности?
Проверка знаний регуляторных ограничений в США при работе с НКО и группами защиты прав пациентов.
Какие основные комплаенс-риски вы видите при организации консультативных советов с пациентами и как вы их минимизируете?
Оценивает навыки кросс-функционального взаимодействия.
Как вы будете разрешать конфликт интересов между требованиями отдела клинических операций (скорость набора) и интересами пациентского сообщества (бремя участия)?
Проверка стратегического видения в контексте редких заболеваний.
Какова ваша стратегия по выстраиванию доверия в сообществах редких заболеваний, где пациенты могут скептически относиться к новым методам генной терапии?
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- Страна
- США
- Зарплата
- 213 000 $ – 261 000 $