Responsibilities:

• Develop and implement global medical TA strategy and plan for GMA activities
• Provide medical leadership, insight and strategy to TA global medical affairs team across functions and countries globally
• Co-lead development of the situational assessment and the global product disease strategy plan
• Oversight of the in-year global medical strategy, real world evidence generation plan, tactical plan and budget for global initiatives
• Providing medical strategic recommendation for late phase pipeline programs and post-approval in-line life cycle management (LCM)
• Contributing to Phase 3b/4 and ESR evidence generation strategy for late phase pipeline and in-line TA programs
• Developing and overseeing clinical study design for late phase pipeline and in-line TA programs
• Set strategy for externally sponsored research (ESR) and review and ensure alignment with TA strategy of proposals
• Providing clear strategic guidance to scientific communication, internal medical training, external medical education, medical info, PEVT teams
• Providing global medical guidance to country medical teams in developing country medical plans aligned with global medical strategy
• Responsible for the global and country quarterly management review

Requirements:

• PhD, PharmD or MD level degree or equivalent
• 1-4 years + experience in medical affairs organization
• Experience developing and implementing launch strategies in global or regional medical affairs functions
• Excellent communication skills both written and verbal
• Understanding of regulatory and compliance for a medical affairs organization
• Excellent interpersonal skills with demonstrated track record and ability to drive results as an effective a team member and project leader
• Proven ability to manage budget and resources
• Strong business acumen
• Ability to build partnerships cross-functionally
• Flexibility and ability to adapt to changing conditions
• Excellent problem solving, organizational, and negotiating skills
• Must demonstrate an energy and enthusiasm which brings a positive approach to all challenges
• Sense of ethics and responsibility

Preferred Qualifications:

• Experience leading cross-functional teams
• Experience in haematology, nephrology or solid organ transplant
• Experience in the Pharmaceutical or biotechnology industry
• Rare Disease Experience

Benefits:

• Annual base pay ranging from $206,827.20 to $310,240.80
• Short-term incentive bonus opportunity
• Eligibility to participate in equity-based long-term incentive program
• Retirement contribution
• Commission payment eligibility
• Qualified retirement program [401(k) plan]
• Paid vacation and holidays
• Paid leaves
• Health benefits including medical, prescription drug, dental, and vision coverage

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At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. AstraZeneca holds a unique position in respiratory disease, including asthma and chronic obstructive pulmonary disease (COPD), with a range of differentiated potential medicines in development by leveraging novel combinations, biologics and devices.

Responsibilities

This role is for a field-based professional with scientific, clinical and therapeutic expertise. The Respiratory Medical Science Liaison Respiratory is responsible for providing medical and scientific support for AstraZeneca's marketed products, new indication and compounds in development.

Key Responsibilities:

• Developing relationships and engaging in scientific exchange with medical and scientific partners, including Healthcare Professionals, Quality Assurance Managers, Population Health Experts, and Managed Markets Customers with in Health Systems. Each scientific engagement is focused on Practice Change within the Health System with the ultimate goal of causing Practice Change thus improving medical care for patients with Asthma and/or COPD.

• Partnering with key internal stakeholders including Commercial Account Directors/Managers, Payer Medical, Medical Directors, and Practice Change Champions.

• Identifying pre-clinical, clinical and post-marketing study investigators in alignment with Medical Affairs objectives; and provide impactful information that enhances the value and proper use of AZ products to internal partners.

• Responding to customer inquiries to provide focused and balanced clinical and scientific information that supports the appropriate use of or clinically differentiates AstraZeneca's products and services

Essential Requirements:

• 0-1 years' experience as a Medical Science Liaison in the pharmaceutical industry

• Advanced Clinical/Science Degree required (e.g., MD, PharmD, PhD, MSN, NP, PA, etc.). BSN with extensive clinical experience may be considered.

• Knowledge of Health Systems, customer segments and market dynamics

• Demonstrated expertise in discussing scientific content and context to multiple audiences

• Experience initiating Practice Change within Health Systems

• Excellent project management ability

• Excellent oral and written communication and interpersonal skills

• Working knowledge of Microsoft Office Suite

• Thorough knowledge of regulatory environment

• Experience in the pharmaceutical industry

• Strong leadership capabilities

• Must reside in territory

• Ability to travel (50-70%) – percentage varies with geography

Desirable Requirements:

• 2+ years' experience as a Medical Science Liaison in the pharmaceutical industry

• Established track record of basic or clinical research

• Proven expertise in the drug discovery and drug development process

• Previous experience working within Health Systems or Integrated Delivery Networks

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting-edge methods and bringing unexpected teams together.

Ready to make a difference? Apply today and join our mission to change lives!

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As an Amyloidosis (ATTR) Medical Science Liaison (MSL), you’ll play a pivotal role in channeling our scientific expertise to positively impact patient care. You will be part of AstraZeneca’s mission to transform clinical practice through science and technology. You’ll partner with healthcare professionals to reduce acute episodes, disease complications, hospital admissions, and premature death. Through innovation, leadership, and sustainability, we put patients first.

In this field-based role covering NYC (Bronx, Brooklyn, Queens and Long Island) and surrounding areas you will:

Engage and build relationships: Develop and maintain strong connections with heart failure specialists, cardiologists, and key opinion leaders (KOLs) in cardiovascular and amyloid disease areas

Scientific exchange and insights: Collect, analyze, and share evidence-based insights while leveraging territory relationships to accelerate knowledge transfer and influence clinical practice

ATTR-CM expertise: Apply prior experience or meaningful exposure to ATTR cardiomyopathy in field activities and translate complex scientific data into clear, clinician-ready insights

Education and collaboration: Support clinician education, deliver presentations, and provide clinical guidance at regional and national meetings

Patient-focused impact: Identify opportunities to improve patient outcomes and provide actionable insights to internal teams

Regulatory and product knowledge: Respond to inquiries with clear, balanced scientific information while ensuring compliance with regulatory and company standards

Continuous learning: Stay current on disease state management, emerging therapies, and the competitive landscape

Development Opportunities - Structured onboarding and continuous learning programs - Exposure to clinical development activities and therapeutic brand strategies - Opportunities to lead projects within the medical team and develop leadership skills over time

Minimum Requirements - Bachelor’s Degree in a clinical or scientific field - 1–2 years of clinical experience in ATTR, Heart Failure, Cardiology and/or pharmaceutical experience with exposure to cardiovascular or amyloidosis disease areas, including KOL engagement, scientific exchange, and territory-based field activities - Understanding of healthcare delivery systems, payer structures, and treatment pathways - Clinical experience in the relevant therapeutic area and ability to build professional relationships - Strong communication skills to convey complex scientific information clearly - Demonstrated ability to lead projects and influence cross-functional teams - Knowledge of regulatory and compliance requirements related to medical affairs - Ability to travel 50–70% (varies by geography), including weekends and overnights

Desirable Requirements - Advanced degree in a clinical or scientific field (MD, PharmD, PhD, NP, PA) - 2+ years of pharmaceutical industry experience / previous MSL experience in ATTR - Rare Disease and/or Cardiology experience - Ability to build and leverage relationships to influence outcomes that improve patient care

The annual base pay for this position ranges from $160,396 – $240,594 USD. Our positions offer eligibility for various incentives, including short-term bonuses, equity-based awards for salaried roles, and commissions for sales roles. Benefits include retirement programs, paid time off, and health, dental, and vision coverage in accordance with applicable plans.

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This role is accountable for shaping and executing the medical strategy across the product launch and lifecycle, with a strong emphasis on launch readiness, US medical affairs strategy, evidence generation, cross-functional coordination, and external scientific engagement.

The primary responsibilities of this role are to:

• Lead strategic planning and execution of US and global Medical Affairs strategy for the cardiovascular radiotracer portfolio;
• Translate strategy into integrated medical tactics and coordinate cross-functional execution;
• Lead, author, own launch readiness medical strategy and plan according to priorities agreed within the multifunctional Product Team;
• Support and shape the US and global evidence generation strategy including IIRs, RWE, and publication activities;
• Participate in medical and promotional review committees ensuring scientific rigor and compliance;
• Ensure seamless and coordinated partnership with Field Medical leadership to achieve integration of insights into strategy development and execution;
• Establishes new and grow existing critical external relationships with US and global thought leaders and professional societies relevant to the cardiovascular molecular imaging portfolio;
• Lead medical engagement planning including advisory boards and scientific exchange;
• Active member and individual contributor in multidisciplinary Product Development Teams and Product Teams;
• Represent Medical Affairs at national and international scientific congresses and conferences;
• Manage key stakeholders including Global Medical Affairs, Commercial teams, and other internal partners;
• Ensure timely and appropriate management of the medical affairs budget and expenditure.

We seek an incumbent who possesses the following:

• A breadth of diverse leadership experiences and capabilities including the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

Required Qualifications:

• MD or PhD with industry experience required;
• Experience in Medical Affairs required, including past roles as a Medical Affairs lead individual contributor in multifunctional Product Teams;
• Strong strategic thinking, leadership, and scientific communication skills;
• Customer-oriented approach and ability to work in cross-functional teams;
• Proven strategic thinking skills and ability to interpret and implement strategic directions;
• Ability to manage multiple tasks and deal effectively with deadlines;
• Creativity, resourcefulness, high energy and flexibility;
• Excellent verbal and written communication skills;
• Strong Business acumen.

Preferred Qualifications:

• MD is preferred;
• 3-5+ years industry experience - Experience in cardiovascular molecular imaging, cardiac and/or systemic amyloidosis or related therapeutic areas preferred;
• Experience in product launch strongly preferred;
• Knowledge of clinical studies, real-world evidence, health care economics and its impact on medical decision making desired;
• Strong VACC (Visionary, Architect, Catalyst, Coach) attributes.

Employees can expect to be paid a salary of between $185,400 to $278,100. Additional compensation may include a bonus or commission (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc..

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The successful candidate will be responsible for developing and executing clinical/medical education strategies, providing training via in-person, virtual, and hybrid environments, and serving as medical and scientific support in the field for healthcare providers. They will also be responsible for maintaining scientific expertise, engaging with thought leaders, and collaborating with internal business partners.

Key responsibilities include:

• Maintaining scientific expertise through completion of core training curriculum and basic MSL certification, full participation in therapeutic area updates and/or training initiatives, medical conference attendance and reviews, routine self-paced reading of current publications, professional licensure with CEU documentation, and completion of recertification and advanced certification where applicable.

• Direct scientific exchange through presentations to external audiences, timely, accurate, specific, and balanced responses to professional requests for information (PIR) in collaboration with Medical Communications, adherence to SOP and FDA guidance for distribution of scientific information, adherence to SOP and compliance guidelines for all external contacts, preparation and presentation of data to internal audiences, and provision of inputs for developing materials for internal and external use.

• Thought leader engagement through criteria-based selection and validation to identify and confirm thought leader status, routine contacts with thought leaders, research site identification and investigator-initiated research (IIR) support, speaker training and evaluation, advisory board coordination, workshop leadership, and/or presentation at advisory board, and coordination of national/international thought leaders' engagement with senior management and other key internal partners.

• In addition, the successful candidate will identify customer medical/clinical needs and challenges within the suite, clinically and medically differentiate the features and value of Bayer products/solutions and services across the Molecular Imaging product portfolio, assist customers on basic protocol adaptation and answer to any focused/alternative protocols inquiries for the best outcome for patients, ensure a good alignment and collaboration between internal Bayer stakeholders, drive high customer satisfaction and experience, regularly report relevant competitive activity, assist in planning and execution of medical field force initiatives, including training and communications, identify account/hospital influence level for input into commercial segmentation, and drive scientific discussions on patient needs and data gaps, e.g., IIRs.

To be successful in this role, you will need to possess a bachelor's degree, at least two years of industry experience, strong presentation, verbal, and communication skills, excellent oral and written communication skills, excellent interpersonal skills, working knowledge of FDA, OIG requirements, and a valid driver's license and eligibility to drive a company car or pooled vehicle.

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