Medical Affairs Scientist New
CPL Dublin
ROLE SUMMARY
- The Medical Affairs Scientist (MAS) is a key scientific ambassador for Pfizer, building long-term partnerships with healthcare professionals (HCPs), key opinion leaders (KOLs), and other stakeholders to advance patient outcomes. Operating at the intersection of science, healthcare innovation, and patient impact, as a MAS, your role is central to the success of medical affairs in the Country Cluster Structure.
MAIN REPONSIBILITIES / DUTIES
Insight Generation, Synthesis & Sharing- Engage with HCPs, KOLs, authorities, and scientific stakeholders as a peer, fostering trust and credibility in all
- Generate, document, synthesize, and compliantly share actionable medical insights from external engagements,
- Effectively disseminate key scientific insights using omnichannel and digital platforms, ensuring relevant
- Ensure insights are communicated effectively to cluster medical leadership, cross-functional teams, and relevant
- Support the Country Medical Lead (CML) in external engagement, acting as a visible and credible representative
of Pfizer Medical in the market.
External Engagement & Stakeholder Management- Formulate and execute a prioritized and impactful medical plan, including KOL mapping. Use metrics to learn
- Execute, manage and lead local projects, events and omnichannel activities in alignment with cluster and
- Build and optimize enduring relationships with external stakeholders, including medical societies, regulators,
- Actively participate in external forums and scientific events, representing Pfizer’s medical interests and supporting the CML’s leadership in these settings.
- Serve as a scientific point of contact for assigned therapeutic areas in-country, collaborating with above country cluster Scientific Experts and other internal stakeholders.
- Targeted support of the local clinical trial environment including protocol feasibility, site identification, investigator engagement, and supporting recruitment.
- Compliantly share stakeholder insights internally to identify collaboration opportunities and drive cross-functional alignment.
- Collaborate with cluster medical, access, regulatory, clinical, and commercial teams to support integrated planning and execution.
- Inform and contribute to the execution of cluster-level medical and brand strategies in alignment with global and International goals.
- Uphold the highest ethical standards, scientific integrity, and compliance in all activities.
- Take responsibility for own learning, ensuring your skills and knowledge are up to date.
- Support regulatory and pharmacovigilance departments for compliance activities (safety updates, product supply issues, etc.).
- Advanced healthcare or scientific degree coupled with deep pharmaceutical experience and knowledge. A
medical degree (MD) or equivalent and board certification, or TA-related PhD and post-doctoral experience is
desirable.- Robust scientific and medical experience, including clinical or research experience.
- Knowledge of the pharmaceutical industry, local healthcare systems, and regulatory environments.
- Demonstrated ability to analyze medical data and generate insights.
- Fluent business and medical English (additional languages as required by market).
- External Stakeholders: Healthcare professionals (HCPs), including physicians, pharmacists, and clinical
investigators; Key Opinion Leaders (KOLs) and scientific experts in assigned therapeutic areas; Medical
societies, professional associations, and academic institutions; Regulatory authorities, payors, and government
health agencies; Patient advocacy groups and relevant non-governmental organizations; Contributors to
national formularies.- Internal Stakeholders: Country Medical Lead (CML), supporting external engagement and strategic initiatives;
and Brand Teams; Cluster medical leadership and international medical colleagues.
RESOURCES MANAGED- Financial Accountability: The MAS may contribute to budget planning and oversight for medical initiatives, scientific events, and evidence generation activities, working collaboratively with the Country Medical Lead and cross-functional teams to ensure resources are used efficiently to maximize patient and business impact.
- People Management:
This role is an individual contributor.
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