This is an exciting opportunity to Join a Rapidly Growing Biotech Company as Clinical Program Head in Basel
Our biotech client based in the city of Basel is seeking an experienced and driven individual to join their team as a Head of Clinical Program Management (M/W/D) . Our client is focused on developing next-generation oncology products, with the aim of bringing new hope to cancer patients worldwide. This is an exciting opportunity to work for a company that is dedicated to making a real difference in the lives of others.
Responsibilities:
As the Clinical Program Head, you will be responsible for overseeing clinical development programs from Phase I through regulatory submission. This includes developing protocols, study reports, investigator brochures and other relevant documentation. You will also manage cross-functional teams including medical affairs, data management and statistical analysis groups. Your expertise and leadership skills will be utilised to ensure the successful execution of clinical trials and programs.
As the Clinical Program Head, you will be involved in the development of the clinical development strategy, and will work closely with the senior management team to ensure that this is aligned with the overall corporate strategy. You will have a key role in the development of the annual clinical development plan, and will be responsible for the delivery of this plan within the agreed timelines and budget.
Experience / Professional Requirements:
- MD degree
- Advanced knowledge in relevant disease area(s) is essential.
- Minimum of 6 years of experience in clinical drug development, including demonstrated leadership and accomplishments in designing and conducting clinical trials (e.g., planning, executing, reporting, and publishing).
- People management experience is required, including matrix management.
Required Competencies:
- Ability to leverage scientific, clinical, and technical knowledge with excellent communication skills.
- A strategic thinker with strong influencing and negotiation skills; regulatory experience would be advantageous.
- Possesses excellent organisational skills.
- Demonstrates knowledge of Good Clinical Practice, clinical trial design, and the drug development process.
- Has a working knowledge of oncology- and nuclear medicine-specific aspects of clinical development.
- Able to travel internationally (anticipated requirement: 20% of the time).
- Fluent in English (both oral and written).
As the Clinical Program Head, you will be required to work closely with a range of stakeholders, including clinical investigators, regulatory authorities, and key opinion leaders. You will need to be able to build effective working relationships with these stakeholders, and will be expected to represent the company at external meetings and conferences.
Our client is committed to the development of its employees, and as such, the successful candidate will have access to a range of training and development opportunities. These will include both internal and external training courses, and the opportunity to attend industry conferences and events.
If you're interested in joining this dynamic company working towards finding solutions that will change people's lives forever then please apply today! This is an exciting opportunity to work for a company that is dedicated to making a real difference in the world of oncology.
