Development Program Lead Science & Innovation (m/f/d)

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Dr. Falk Pharma GmbH
Munkavégzés helye

Hibrid

Munkaidő, foglalkoztatás jellege
- Alkalmazotti jogviszony
- Általános munkarend
Elvárások
- Angol középfok
- 1-3 év tapasztalat
- Középiskola

Állás elmentve

A hirdetést eltávolítottuk a mentett állásai közül.

Responsibilities

Your tasks

The Development Program Lead (DPL) is responsible for the strategic and operational management of a development program from the early stages through to approval.

The DPL develops the cross-functional development strategy in collaboration with the Integrated Development Team (IDT), oversees its implementation across all functions, and serves as the central point of contact for the Steering Committee and external partners. The IDT consists of the following functions: Pre- & Early Clinical Research, Clinical Research, CMC Project Management, Global Safety, Global Medical, Global Commercial New Products, Global Market Access, Intellectual Property and Technical Operations.

Key Responsibilities:

The DPL and IDT ensure that the project is advanced in a scientifically sound, efficient, and regulatory-compliant manner, with optimal use of resources
The DPL should possess a broad, cross-functional skill set and act less as a subject matter expert (SME) in a single area
When development programs are carried out in collaboration with external partners, the DPL also assumes the role of the Alliance Manager
The DPL assists in coordinating timelines, risks, resources, and budgets across programs with the Head of CPMO and the Steering Committee
The DPL implements project management standards, processes, and templates across all pre-clinical and clinical projects

Requirements

Your qualification

Degree in a medical or scientific field
Several years of experience in drug development (e.g., preclinical or clinical development in Phases I–III) and cross-functional program management
Strong project management skills (certification PMI, Prince2 or similar highly preferred) with a minimum of 5 years project management experience
Experience in a regulated work environment
In-depth knowledge of GxP and regulatory standards
Industry experience (pharmaceuticals or biotechnology)
Basic knowledge of hepatology and gastroenterology is a plus

Furthermore:

Strong leadership and influence skills within a matrix organization
Experience leading cross-functional teams
Excellent communication skills in English; German language is beneficial
Ability to present complex scientific content clearly, precisely, and in a manner tailored to the target audience
Strong decision-making skills and sovereignty in dynamic or uncertain situations; ability to make high-quality decisions under time pressure
We support hybrid working arrangements: remote work is possible, but we place value on consistent on-site presence to ensure effective teamwork and communication

What we offer

Your benefits

Supportive, respectful and appreciative work atmosphere in a small, dedicated team
Diverse learning culture and individual development opportunities
International and growing family business with short decision-making processes, financial independence and long-term perspective
New work, flexible working hours and mobile working
Wide range of benefits (free beverages, health and sports benefits, canteen, JobRad)
Comprehensive onboarding and mentoring program

If you have any questions, please do not hesitate to contact Sabine Aicher at online portal.

Company info

As the experts in digestive and metabolic medicine and as a family-owned business with a global presence, we focus on developing and marketing innovative medicines to treat a wide range of gastrointestinal disorders like inflammatory bowel disease or eosinophilic esophagitis as well as hepatobiliary disorders such as primary biliary cholangitis. Our aim: to meaningfully improve therapeutic practice as well as patient health and well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: