Senior Medical Manager - Oncology, EU & Int'l

Azurity Pharmaceuticals - Ireland; Dublin; On-site; EUR 110,000 - 150,000; Full time

Job summary

Azurity Pharmaceuticals in Dublin seeks a Senior Medical Manager – Oncology, EU & Int'l to lead medical strategy and liaise with HCPs, KOLs, and academia. You will oversee advisory boards, publications, and cross-functional collaboration across clinical development, regulatory, and commercial teams.

The role emphasizes scientific leadership, strategic planning, and effective external engagement in a dynamic, office-based setting with in-person collaboration 3 days a week.

Qualifications

• Advanced terminal degree required.
• 2-3 years relevant experience in clinical, fellowship, or pharmaceutical industry settings.

Responsibilities

• Develop and execute an integrated Medical Affairs strategy aligned with brand objectives and corporate priorities.
• Serve as scientific and clinical expert across product lifecycle including pre-launch, launch, and post-marketing support.
• Support and sustain relationships with key opinion leaders (KOLs) and external scientific stakeholders.
• Plan and support advisory boards, investigator meetings, and scientific symposia.
• Support development, review, and approval of medical materials and publication planning.
• Provide strategic medical input for conference planning and on-site execution.
• Collaborate with cross-functional teams (Clinical Development, Regulatory, Commercial, Market Access, Pharmacovigilance).
• Support medical training and ongoing clinical guidance for sales and internal teams.
• Assist with Real-World Evidence and investigator-initiated studies as needed.

Skills

Interpersonal skills

Oral presentations

Scientific expertise

Strategic thinking

Operational execution

Cross-functional collaboration

Time management

Education

Advanced terminal degree (PharmD, PhD, MD, DO, DNP) OR other advanced medical (NP, PA, RN etc.)

Job description

Senior Medical Manager - Oncology, EU & Int'l

Dublin

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com .

Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

"Azurity roles are office based and are generally require individuals to be in office Tuesday through Thursday with Monday and Friday as optional days."

About the Role

Medical Affairs at Azurity Pharmaceuticals, a privately held company delivering innovative medicines for overlooked patients across 50+ countries, drives scientific and clinical initiatives with a portfolio of 30+ brands spanning 10 dosage forms and 9 therapeutic areas. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

The Senior Medical Manager - Oncology, EU & Int'l is a EU-based position within the Medical Affairs Department, reporting to the VP Head of Medical - ONCO. The role holder is responsible for leading and executing medical strategy to support the safe, effective, and evidence-based use of the company’s products. This role serves as a scientific expert and key liaison between internal teams and external stakeholders, including healthcare professionals (HCPs), key opinion leaders (KOLs), and academic institutions.

• Develop and execute an integrated Medical Affairs strategy aligned with brand objectives and overall corporate priorities.
• Serve as a scientific and clinical expert across the full product lifecycle, including pre‑launch planning, launch execution, and post‑marketing support.
• Support and sustain strong relationships with key opinion leaders (KOLs) and other external scientific stakeholders.
• Plan and support advisory boards, investigator meetings, and scientific symposia to advance scientific understanding and gather actionable insights.
• Support the development, review, and approval of medical materials (e.g., slide decks, FAQs, training content) and support publication planning and execution (abstracts, posters, manuscripts) in close collaboration with Medical Excellence
• Support stakeholder engagement and education planning in close collaboration with Medical Leads
• Provide strategic medical input for conference planning, scientific content, and on‑site execution.
• Partner cross‑functionally with Clinical Development, Regulatory Affairs, Commercial, Market Access, and Pharmacovigilance to ensure aligned and effective execution of medical strategy.
• Support sales and internal teams through medical training, scientific education, and ongoing clinical guidance.
• Support real‑world evidence (RWE), investigator‑initiated studies (IIS), and post‑marketing studies in collaboration with Clinical Development as needed.
• Collaborate with field medical team to analyze medical insights from external engagements to inform medical strategy and lifecycle planning.
• Apply all Medical Affairs SOPs, regulatory, legal, and compliance guidelines while executing activities.
• Demonstrate adaptability, focus, and composure in fast-paced settings while operating with minimal direction.

Qualifications and Education Requirements

Education:

• Advanced terminal degree (PharmD, PhD, MD, DO,DNP) OR other advanced medical (NP, PA, RN etc.) is required.

Experience:

• 2-3 years relevant work exp (clinical, fellowship, or research experience) and/or related pharmaceutical industry work experience is required.
• Thorough knowledge or experience in cardiovascular, obesity, renal or endocrine related diseases.

Skills:

• Excellent interpersonal and communication skills with a passion for excellence
• Demonstrated ability to present effective and influential oral presentations
• Deep scientific expertise - stays abreast of data, treatment trends, and new information in the profession and ability to articulate therapeutic knowledge and translate expert feedback into appropriate insights
• Strong strategic and operational thinking skills, with the ability to manage effective networks
• Ability to work effectively in a time and independently
• Highly collaborative team player with experience working across cross-functional teams.
• Excellent organization skills and decision-making abilities. Skillfully plans, prioritizes, and executes multiple responsibilities and projects.
• Knowledge of relevant US healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends.
• Travel: Up to 30-40% travel to attend medical conferences, engage with KOLs, and support strategic activities within the US.

I acknowledge that I have read the Azurity Candidate Privacy Notice ( https://azurity.com/candidate-privacy-notice/ ) and understand that Azurity Pharmaceuticals, Inc. will process my personal information for recruitment and hiring purposes, including reviewing my application, assessing my qualifications, communicating with me, conducting interview and selection activities, and complying with applicable legal and regulatory obligations.

I understand that certain information requested during the application process may be considered sensitive or special-category information under applicable privacy laws, such as demographic, disability, veteran status, accommodation-related, or equal employment opportunity information. Where such information is requested, I understand that providing it is voluntary unless otherwise required by law, and that Azurity will use it for recruitment administration, legal compliance, equal employment opportunity reporting, accommodations, and related purposes described in the Candidate Privacy Notice.

Voluntary Self-Identification

For government reporting purposes, we ask candidates to respond to the below self-identification survey.Completion of the form is entirely voluntary. Whatever your decision, it will not be considered in the hiringprocess or thereafter. Any information that you do provide will be recorded and maintained in aconfidential file.

As set forth in Azurity Pharmaceuticals - Ireland’s Equal Employment Opportunity policy,we do not discriminate on the basis of any protected group status under any applicable law.

If you believe you belong to any of the categories of protected veterans listed below, please indicate by making the appropriate selection.As a government contractor subject to the Vietnam Era Veterans Readjustment Assistance Act (VEVRAA), we request this information in order to measurethe effectiveness of the outreach and positive recruitment efforts we undertake pursuant to VEVRAA. Classification of protected categoriesis as follows:

A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.

A "recently separated veteran" means any veteran during the three-year period beginning on the date of such veteran's discharge or release from active duty in the U.S. military, ground, naval, or air service.

An "active duty wartime or campaign badge veteran" means a veteran who served on active duty in the U.S. military, ground, naval or air service during a war, or in a campaign or expedition for which a campaign badge has been authorized under the laws administered by the Department of Defense.

An "Armed forces service medal veteran" means a veteran who, while serving on active duty in the U.S. military, ground, naval or air service, participated in a United States military operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985.