Clinical Program Head in Basel bei Ariceum Therapeutics GmbH

Clinical Program Head
Ariceum Therapeutics GmbH is a rapidly growing clinical stage oncology company focused
on developing next generation radiopharmaceutical oncology products. The product pipeline
includes satoreotide, a potent antagonist with high affinity for tumour cells expressing SST2
receptors. Satoreotide is being developed into products with complementary therapeutic and
diagnostic imaging opportunities in a range of solid tumours. Ariceum Therapeutics GmbH is
headquartered in Berlin with a subsidiary in Basel and employees in a number of European
countries.

Position
Job title: Clinical Program Head
Department/Function: Research and Development
Reports to: Head of R&D / Head of Clinical Development
Number of reports 0-2 direct reports, matrix management of cross-functional teams
Financial responsibility N.A.
Location of the role: Basel (office based with hybrid component)

Main Purpose of the Position

The Clinical Program Head

• Leads the strategy, scientific design, planning and management of the assigned

development programs

• Develops close working relations with medical experts and investigators in the

relevant disease area(s) and represents Ariceum Therapeutics in scientific and
regulatory meetings

• Oversees resource allocation and budget for the assigned programs
• Actively contributes to build an empowered organization that can adjust quickly to

business needs.

safety related documents, study reports), clinical components of regulatory
documents, clinical communication and publications

• Accountable for Patient Safety of the assigned compounds, including signal detection

and surveillance

• Responsible for resource planning and management for the assigned clinical

programs in close collaboration with finance, program management and other
functions

• Accountable for process development and implementation in compliance with

ICH/GCP and other relevant standards

• Responsible for medical and scientific leadership in interactions with external and

internal stakeholders (e.g., regulatory authorities, key opinion leaders, advisory
boards, patient advocacy groups)

• Responsible to identify risks and mitigation strategies including contingencies
• Contribute to the overall strategy and scenario generation for the R&D portfolio,

support the Head of R&D to align the organization behind agreed strategy

leadership and accomplishment in designing and conducting clinical trials (e.g.,
planning, executing, reporting and publishing)

• People management experience required, including matrix management