Medical Manager Gene Therapy (Xico)

Medical Manager Gene Therapy (Xico)

01 nov
|
General Management
|
Xico

01 nov

General Management

Xico

Summary
We are looking for a Medical Manager to provide scientific and medical leadership for an assigned Therapeutic Area, helping translate scientific evidence into meaningful impact for patients and the healthcare community.
This role offers the opportunity to work at the intersection of science, clinical research and medical strategy, partnering with leading external experts and internal cross-functional teams. The Medical Manager will build trusted scientific relationships with Key Opinion Leaders (KOLs) and relevant healthcare and regulatory stakeholders, generate actionable medical insights, and contribute to the development and execution of clinical and evidence-generation activities.
About the Role
Main Responsibilities:
Build and maintain strong scientific relationships with
Key Opinion Leaders (KOLs), healthcare professionals and relevant external stakeholders
, fostering high-quality scientific exchange and identifying insights that can inform the medical strategy.
Ensure medical and scientific enquiries are addressed with
high quality and in a timely manner
, in accordance with applicable standards, and develop standard scientific response documents for frequently asked questions when appropriate.
Provide medical and scientific input into the
design, development and execution of clinical trials and clinical research activities
, including the initiation and oversight of studies within the assigned Therapeutic Area.
Support the country strategy and execution of
Non-Interventional Studies (NIS) and Investigator-Initiated Trials (IITs)
, contributing to local evidence-generation priorities.
Contribute medical expertise and scientific insights to the development and execution of the




Therapeutic Area medical strategy and annual medical activities
.
Coordinate the medical review and approval of locally developed medical and promotional materials, ensuring that integral and regional materials are appropriately adapted to local scientific needs and approved according to applicable local and P3 guidelines.
Translate scientific developments, external stakeholder perspectives and medical insights into
actionable recommendations for cross-functional teams
.
Work collaboratively with
Pharmacovigilance, Regulatory Affairs, Market Access, Quality Assurance, Commercial, Brand and other relevant functions
, ensuring the medical perspective is incorporated into strategic discussions and business priorities.
Support scientific and educational initiatives, including advisory boards, congress-related activities, scientific meetings and other medical education activities, as appropriate for the Therapeutic Area.
Identify and assess potential risks within the area of responsibility and contribute to appropriate
risk mitigation plans, internal controls and monitoring activities
.
Ensure all activities are conducted according to the highest standards of
Ethics & Compliance
, applicable regulations and company policies.
Ensure technical complaints, adverse events and special case scenarios related to company products are reported within the required timelines and processes.




Profile Requirements
University degree in
Medicine.
Strong scientific understanding and ability to critically interpret and communicate
clinical and medical evidence
.
Relevant professional experience within
Medical Affairs, clinical research, the pharmaceutical/biotechnology industry or a closely related scientific healthcare environment
.
Experience working within a
Therapeutic Area
and developing a strong understanding of the scientific landscape, patient journey and evolving standards of care.
Experience interacting and developing credible scientific relationships with
KOLs, investigators, healthcare professionals and other external scientific stakeholders
.
Understanding of
clinical research and evidence generation
, including clinical trials, non-interventional studies and/or investigator-initiated research.
Experience collaborating with cross-functional partners such as
Regulatory Affairs, Pharmacovigilance, Market Access, Commercial, Quality and Brand teams
.
Scientific credibility:
Able to understand complex scientific information, critically assess clinical evidence and communicate it clearly to different audiences.
Strategic thinking:
Able to connect scientific developments, stakeholder insights, evidence gaps and patient needs with the broader Medical Affairs strategy.
External stakeholder engagement:
Strong ability to develop trusted, credible and non-promotional scientific relationships with KOLs and healthcare stakeholders.
Communication and influencing:
Excellent presentation, facilitation and communication skills, with the ability to influence across functions without relying on formal

📌 Medical Manager Gene Therapy (Xico)
🏢 General Management
📍 Xico

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