Early Development Asset Lead

Ipsen

8d•Hybrid

About The Position

The Early Development Asset Lead (EDAL) is a scientific and program leadership role within Ipsen's Early Development and Innovation organization, accountable for integrated development strategy and execution for one or more early-stage therapeutic assets from drug candidate nomination through first-in-human clinical trials. The EDAL leads the Early Development Asset Team (EDT), a cross-functional matrix team spanning clinical, regulatory, CMC, translational, clinical pharmacology, nonclinical safety, and biomarkers, ensuring that each program advances with scientific rigor, strategic clarity, and accountability to portfolio decisions. The EDAL maintains alignment with Therapeutic Area strategy to ensure EDT plans support agreed portfolio priorities, and serves as the scientific champion for assigned programs, articulating project goals, scientific rationale, and clinical line of sight internally and externally. Depending on pipeline needs, the EDAL may represent Early Development in due diligence as the ED lead within a multidisciplinary global team.

Requirements

PhD, MD, PharmD, or relevant advanced degree with a minimum of 10-15 years of multidisciplinary drug development experience in the pharmaceutical or biotech industry.
In-depth understanding of oncology required.
Experience with regulatory filings, including IND/CTA authorship and health authority interactions, required.
Strong understanding of drug development from discovery through life cycle management.
Demonstrated experience leading cross-functional early development teams, with accountability for integrated program strategy and governance-level presentations.
Proven scientific and leadership performance in a matrix environment, as evidenced by pipeline contributions, publications, and/or patent applications.
Demonstrated ability to lead decision-making in a multi-regional, diverse matrix environment.
Proficient in written and oral English.
Outstanding communication skills, with the ability to present complex program strategies to senior leadership and governance committees with clarity and scientific credibility.
Ability to build strong relationships with stakeholders across clinical development, clinical operations, translational pharmacology, regulatory, CMC, commercial, medical, and research functions.
Ability to integrate scientific, regulatory, clinical, and commercial perspectives into balanced, portfolio-aligned program strategies.
Strong organizational and project management skills, with the ability to manage multiple priorities and competing timelines.
High emotional intelligence, flexibility, and collaborative mindset, with the ability to seek and evaluate diverse viewpoints.

Nice To Haves

Experience in immuno-oncology and/or ADCs desirable.
Broad cross-functional drug development knowledge, with experience in more than one functional area, such as nonclinical, translational, regulatory, or clinical development, strongly preferred.
Expertise in small molecules, biologics, and novel modalities preferred.
Experience developing and delivering translational strategies, including biomarker and precision medicine approaches in early-phase clinical trials.
French or another European language is an advantage.

Responsibilities

Leads one or more Early Development Asset Teams.
Owns integrated program strategy across preclinical, translational, clinical, diagnostic, and regulatory activities.
Develops and maintains integrated asset strategy, including target product profile, indication strategy, key development options, competitive context, and evidence required for decision-making.
Ensures Early Development plans deliver against agreed Therapeutic Area strategy and portfolio priorities, with clear evidence-based rationale for stage-gate investment decisions.
Integrates input from critical functions and research teams to develop plans that balance scientific risk, timelines, cost, and clinical proof-of-concept potential.
Ensures adequate resources to deliver approved plans, proactively identifies risks, and leads mitigation strategies.
Presents plans, data, risks, options, and recommendations to governance bodies with scientific credibility, while appropriately leveraging functional expertise.
Builds high-functioning teams through clear communication of program vision, roles, responsibilities, and decision-making expectations.
Maintains a collaborative, inclusive team environment through influence, coaching, and active stakeholder alignment.
Serves as the scientific champion for assigned programs, articulating project goals, translational hypotheses, and clinical strategy internally and externally.
Contributes to due diligence for in-licensing opportunities and, depending on experience and pipeline need, may coordinate findings and present recommendations to governance.