Noema Pharma is a biotech company developing ground-breaking therapies to address the most disabling symptoms in orphan conditions of the brain and nervous system. Noema’s research and development is focused on understanding and meeting patient needs using our novel therapies.
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Administration / Fulltime
The TMF Manager is responsible for managing and ensuring the quality, organisation and inspection readiness of all essential clinical trial documentation across Noema Pharma’s programmes. This includes setting up and maintaining the electronic Trial Master File (eTMF), overseeing document filing and tracking, reviewing document quality in both sponsor and CRO systems, and coordinating documentation activities across internal and external teams such as CROs, vendors and clinical sites. You will also act as the point of contact for TMF?related audits and inspections and support corrective actions when needed, while ensuring compliance with SOPs and regulatory guidelines (ICH/GCP/TMF).
Administration / Fulltime
The Senior VP Clinical Sciences leads clinical research and medical strategy for Noema Pharma’s therapeutic programmes, reporting to the Chief Medical Officer. This executive role oversees the design, execution, and interpretation of clinical studies (from early phase through later stages), provides medical leadership and strategy, and ensures scientific integrity and data quality across clinical development. You will serve as a core member of the Research & Development leadership team, act as a medical spokesperson within and outside the company, build strategic relationships with key opinion leaders, and help prepare clinical components of regulatory submissions. Operational leadership, cross?functional collaboration, and oversight of budgets, timelines, external partners (such as CROs), and clinical data interpretation are central to the role.
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Website:
noemapharma.com/
Headquarter:
Basel
Foundation Date:
July 2020
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