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Medical Affairs Manager Gi​/Inflammation

Job in Rome, Italy
Listing for: Altro
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Medical Science Liaison, Medical Science, Clinical Research
Salary/Wage Range or Industry Benchmark: 90000 - 110000 EUR Yearly EUR 90000.00 110000.00 YEAR
Job Description & How to Apply Below
Overview
Strategic Contribution:
Provide medical expertise to shape and execute Takeda’s strategy for Gastrointestinal / Inflammation Therapeutic Area and pipeline products (NPP) by collaborating cross-functionally.

Scientific Leadership:
Offer in-depth scientific insights to ensure alignment with evidence-based medicine for product development, launch, and lifecycle activities.

Stakeholder Engagement:
Strengthen relationships with key opinion leaders (KOLs), healthcare professionals (HCPs), and scientific communities to support medical strategies and advance therapeutic understanding.

Evidence Generation: generate new clinical data and scientific evidence to support both in line / pipeline assets.

Compliance and Training:
Advocate medical compliance to maintain high ethical standards and provide scientific training to internal teams (BUs and PVA) to elevate internal capabilities (scientific updates, newsletters, congress reports).

Accountabilities

Medical Expertise & Strategy :
Support medical strategies development and medical plans implementation across the GI portfolio to align with Takeda’s overall business objectives.

Scientific Support :
Provide medical and scientific input into clinical development plans while ensuring adherence to ethical and regulatory standards.

Stakeholder Engagement :
Build and maintain relationships with key opinion leaders (KOLs), key external experts (KEEs), DOLs (Digital Opinion Leaders), healthcare providers and academic researchers to drive awareness and credibility in GI / Inflammation TA.

Pipeline : provide support to cross-functional launch readiness: pre-launch medical strategy, stakeholder mapping & engagement plan, insight generation, evidence generation, scientific narrative & materials readiness, medical education & training, congresses, advisory boards & expert meetings.

Medical Education :
Plan and deliver scientific training and educational programs for internal teams (e.g. Commercial and PVA) to ensure understanding / alignment on both products and therapeutic areas GI and Inflammation.

Disclosure & Communication :
Manage external communication of scientific data, including presentations at conferences, advisory boards and other scientific platforms.

Cross-Functional Collaboration :
Partner with marketing, regulatory, PVA and commercial teams to provide medical input to co-create strategies and effectively achieve GI & Inflammation TAs objectives.

Evidence Generation :
Collaborate on real-world evidence generation, R&D clinical trials (active participation in the Global Enterprise Engagement Project) and publication strategies to support Takeda’s product lifecycle management. Discuss and collect independent research proposals (IIRs) according to the company guidelines and related SOPs.

Product Launch Activities :
Provide guidance in the preparation and execution of product launches by delivering medical and scientific support while ensuring compliance with industry standards.

PVA support :
Coordinate with PVA teams both for JCA activities, product dossier submissions, providing scientific expertise and scientific documentation to ensure successful outcomes.

Regulatory support : coordinate with the regulatory team to ensure support to regulatory activities.

Budget : support budget management allocated to medical projects and congresses delegations according to TA medical plans and congress plans.

Education, Behavioural Competencies and Skills
Education and experience

Education requirements:

Medical Degree (MD);
Pharm

D or PhD.

More than 3 years of experience in medical affairs roles.

Good written and spoken English (minimum level required : Intermediate B1).

Knowledge

Basic knowledge of pharma industry legislation

Drug Development and Marketing processes and requirements

Clinical research regulatory environment, including but not limited to ICH GCP and Dir 536 / 2014

Technical skills

Ability to engage with KOL community based on existing strong relationships and ability to build lasting relationships with KOLs.

Thorough understanding of life cycle management.

Experience with working in pre-launch phase and launch preparation.

Ability to interpret and communicate scientific /…
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