Project Lead * (Reporting to the CMO)

Permanent employee, Full-time · Hybrid

Your mission

In collaboration with senior management and the team, the Project Lead* will be responsible development of the disease area strategy of the program and for generating the development plans to achieve this strategy, by closely interacting with internal and external experts. The Project Lead*, based in UK, Germany or France will report to the Chief Medical Officer.

Responsibilities

Leadership of a cross-functional project team to drive the development of a molecule to key go/no-go decisions, milestones or investment timepoints
Responsible for the generation of the disease area strategy, including the Target Product Profile, with respect to the competitor landscape, and generation of the development plans in collaboration with the project team
Highly skilled at inspiring and managing matrix teams through complex challenges and problem solving
Excellent project management skills including development of scenarios, balancing risk, timelines, cost and the probability of success to support decision-making
Plans and justifies required resources and budget for successful project completion, including missing functions in house
Coordinates the project team and the project-related activities
Must have a complete overview of the project at any given time
Supervises the progress of the project with respect to quality, timelines, costs /budgets, strategy / changes, IP protection
Identifies bottlenecks and possible risks, outlines solutions and implements them with the team
Selects/keeps good contact with external experts and KOLs
Ensuring that all project-related documents are appropriately maintained (e.g., agendas and minutes) and filed
Responsible for overviewing the update and completion of Due Diligence data room for projects
Represents the project in presentations and communications to third parties
Generates a publication strategy and implements it with the team

Your profile

PhD in natural science or health science or MD or other adequate title
At least 10 years’ experience in the pharmaceutical industry in an international environment with practical knowledge as project leader with excellent expertise in overall drug development
Good understanding of certain aspects of drug development and launch preparation, e.g. safety pharmacology, pharmacokinetics, toxicology, CMC, clinical development, competitor analysis and regulatory requirements
Clear scientific and medical understanding of the relevant indications, competitive drugs in the market and in development
Very good organizational skills including the capability of setting priorities, being accurate and able to maintain a complete overview of the project
Ability to communicate information effectively
Team-oriented personality with excellent interpersonal skills, i.e., positive and constructive attitude, desire and ability to work in interdisciplinary teams; very strong leader with ability to motivate and inspire their team members
Ability to work in a project-driven and results-oriented way, also in stressful situations
Ability to work independently and with self-motivation under tight timelines
Good knowledge of standard and specific software (e.g., Microsoft Office and Project)
Good English (oral and written) and German (advantageous but not a primary requirement) language skills

Why us?

Unique corporate culture: Scientific excellence, a collaborative working environment and the passion to improve the lives of patients defines our work. With us, you can work together with innovation awarded experts with the proven ability to translate science into commercial success. You can expect diversity, inspiration, as well as trustful collaboration.
Development: We encourage people to grow and strongly support individual development and learning opportunities.
Flexibility: Embracing flexible working accommodations, we enable our people to integrate business into their personal life.
Benefits: Competitive comprehensive benefit plan.

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About us

AiCuris is meeting the needs of the growing population of immunocompromised people who require precise therapies to effectively treat infection. Our flagship product, PREVYMIS, marketed by our partner MSD, treats CMV in a defined group of transplant recipients. Our pivotal phase 3 candidate Pritelivir aims to address recurrent and resistant HSV infections in a broad population of patients with weakened immune systems. For immunocompromised people, an otherwise manageable infection can mean life or death. AiCuris, with its expertise and growing pipeline, is committed to providing therapeutic solutions for them now and in the future.

Passionate about our mission to develop anti-infective therapeutics for patients in need, a team of internationally recognized experts is driving our research and development to improve the lives of patients. We believe in a culture of trust and transparency, where feedback is considered an opportunity to contribute to each other's personal and professional growth. We hire people who are collaborative, adaptable, communicate well, and love to learn.

*AiCuris is an employer that supports equal opportunities, diversity and inclusion. We welcome applications from people regardless of their national origin, skin color, religion, gender, age, marital status, disability, sexual orientation, gender identity or other legally protected characteristics.

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Your application!

We appreciate your interest in our company. Please fill in the following short form. Should you have any difficulties in uploading your files, please contact us by mail at jobs@Aicuris.com.