•

Advanced scientific or healthcare degree such as a PharmD, PhD, MD, DO, or another relevant advanced degree.

•

Four or more years of relevant pharmaceutical industry experience preferred, including experience within Medical Affairs.

•

Strong scientific and clinical acumen, including knowledge of medical terminology, clinical study design, biostatistics, evidence appraisal, and interpretation of clinical and real-world evidence.

•

Demonstrated ability to critically evaluate and synthesize complex scientific, clinical, safety, and technical information and translate findings into clear, balanced recommendations.

•

Strong scientific writing and communication capabilities, including experience developing medical education materials, evidence summaries, abstracts, posters, manuscripts, presentations, and other scientific content.

•

Working knowledge of publication standards, copyright requirements, scientific exchange principles, and applicable Medical Affairs laws, regulations, industry guidance, and internal requirements.

•

Ability to establish credible and compliant relationships with KTLs, healthcare professionals, and external scientific experts.

•

Strong presentation skills and the ability to adapt complex scientific information for scientific, executive, and cross-functional audiences.

•

Strategic thinking, sound judgment, and the ability to connect scientific evidence and stakeholder insights with broader Medical Affairs priorities.

•

Demonstrated ability to collaborate and influence cross-functional stakeholders while maintaining appropriate Medical Affairs independence.

•

Strong project and program management skills, including the ability to manage multiple priorities, complex workstreams, and time-sensitive deliverables.

•

Ability to aggregate and synthesize insights to identify evidence gaps, educational needs, stakeholder barriers, and strategic opportunities.

•

Strong awareness of quality, compliance, and risk, including the ability to recognize and appropriately escalate safety, product quality, and compliance information.

•

Prior experience in Pharmacovigilance, Medical Information, or product complaints is preferred; the ability to complete role-based training and provide designated backup support is required.

•

Experience with KTL engagement, scientific exchange, congress planning or coverage, and scientific communications is preferred.

•

Strong organizational, stakeholder-management, communication, and presentation skills.

•

High degree of accountability, adaptability, integrity, discretion, and commitment to continuous improvement.

•

Ability to work independently within a lean, cross-functional environment and exercise sound judgment when managing competing priorities and potential risks.

•

Fluent English communication skills and willingness to travel overnight up to approximately 20%, including for scientific congresses and external stakeholder engagements.

•

Flexibility to occasionally work evenings or weekends when required by congress schedules or external engagements.