Senior Global Clinical Program Director

At Ribocure, we are driven by science and innovation, with a mission to establish a world-leading company in RNA research and

development, ultimately making a positive impact on patients worldwide. We are seeking a Senior Global Clinical Program Director

to join our growing Clinical Operations team and take a leadership role in driving the successful execution of our clinical

development programs. The final title and level will be determined based on the candidate’s qualifications, experience, and

demonstrated leadership capabilities. Candidates who do not fully meet the requirements for the Senior level may be considered for

appointment as Global Clinical Program Director.

In this role, you will lead clinical programs across all phases of development, driving the strategic development and execution of

the Clinical Development Plan (CDP). You will provide program leadership and oversight across multiple clinical development

activities, ensuring alignment between program objectives, development strategy, operational execution, and regulatory

requirements. You will lead cross-functional teams, coordinate internal stakeholders and external partners, and oversee all

aspects of program planning, governance, risk management, and delivery.

We are looking for a candidate with extensive experience in clinical program leadership in the pharmaceutical/biotech industry,

strong leadership skills, and the ability to combine strategic vision with hands-on execution in a fast-paced, innovative

environment.

• Lead the Clinical Project Team (CPT), driving program strategy, cross-functional alignment, and delivery of the Clinical

Development Plan (CDP)

• Establish the team structure and ways of working required to build a high-performing CPT, ensuring strong Clinical Operations

leadership and effective cross-functional collaboration across functions including Medical, Clinical Pharmacology, Regulatory

Affairs, and Biostatistics.

• Serve as the Clinical Operations representative in the Global Project Team (GPT), contributing to overall program strategy,

governance, and clinical development and execution planning.

• Provide program leadership and direction to ensure adherence to scope, quality, budget, timelines, and proactive risk

management; escalate key program issues to the Global Project Team (GPT).

• Accountable for Clinical Operations deliverables supporting regulatory submissions, regulatory interactions, clinical study

reports, and inspection readiness activities.

• Oversee planning, start-up, conduct, reporting, and close-out of clinical trials, ensuring compliance with regulatory

requirements, GCP/ICH, and industry standards.

• Build and maintain effective relationships with investigators, clinical sites, and key external stakeholders to support program

execution and successful trial delivery.

• Extensive experience across the product life cycle with experience in late-stage development and ideally across multiple

therapeutic areas

We offer more than a job – we offer a mission. You’ll be part of a tight-knit, friendly team working on real challenges with real

potential. Your ideas matter. Your work matters. And your growth matters to us.

We encourage you to submit your CV and cover letter promptly, as applications will be reviewed on an ongoing basis. Final

application deadline: 15 Sep 2026.