Medical Access Manager – MD

Pharma Point; Italia; Remote; EUR 50,000 - 70,000; Full time

Job summary

A leading pharmaceutical company is seeking a medically qualified professional to support Market Access Strategy in Italy. This remote position involves developing medical-scientific content for NHS Pricing & Reimbursement dossiers, coordinating evidence generation projects, and collaborating with cross-functional teams to ensure patient access. Candidates should have 3–5+ years of experience in pharma, focusing on Medical Affairs and Market Access, along with a Degree in Medicine (MD).

Qualifications

• 3–5+ years experience in pharma/biotech.
• Strong command of medical evidence.
• Ability to communicate effectively with stakeholders.

Responsibilities

• Develop medical-scientific backbone for NHS P&R dossiers.
• Partner with cross-functional teams for evidence generation.
• Interface with Regulatory Affairs on lifecycle priorities.

Skills

Medical Affairs experience

Market Access knowledge

Strong communication skills

Education

University Degree in Medicine (MD)

Job description

We’re looking for a medically qualified professional to support Market Access Strategy, ensuring our portfolio is positioned for timely and appropriate patient access.

This is a high-impact role at the intersection of clinical science, evidence generation and reimbursement pathways, with direct contribution to NHS Pricing & Reimbursement (P&R) and regional access activities.

Mandatory: University Degree in Medicine (MD)

What you’ll do

• Develop the medical-scientific backbone of national P&R dossiers to secure and maintain NHS reimbursement.
• Craft scientific value narratives: clinical profile, unmet need, epidemiology, burden of disease, and integration of Real-World Evidence (RWE).
• Drive evidence-generation projects (e.g., epidemiology and RWE initiatives) aligned with local requirements.
• Partner with cross-functional teams and coordinate external experts (KOLs, advisors, consultants).
• Act as the scientific reference for Institutional & Regional Access (RAAM) teams, supporting compliant, high-quality materials and stakeholder initiatives.
• Interface with Regulatory Affairs on selected lifecycle priorities and support medical-scientific governance of internal/external communications.

What you’ll bring

• 3–5+ years in pharma/biotech within Medical Affairs, Market Access/HEOR, and/or Regulatory.
• Strong command of medical evidence (trials, meta-analyses, RWE; ideally exposure to pharmacoeconomics).
• Clear, influential communication style with both technical and non-technical stakeholders.

Location: Italy (Remote-based)

We are proud to be an equal opportunity employer. We don’t discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.