SENIOR CLINICAL RESEARCH CONSULTING
Clinical Research Consulting & Interim Management
Dr. Schaub – Clinical Research Services provides independent senior-level consulting and interim management for pharmaceutical and biotechnology companies.
With more than 20 years of international clinical development experience, I support clinical trial projects with a strong focus on quality, compliance, timelines and operational feasibility.
CLINICAL RESEARCH CONSULTING
Independent senior-level support for global and regional clinical trial projects, tailored to the specific needs of pharmaceutical and biotechnology companies.
GLOBAL CLINICAL TRIAL MANAGEMENT
Operational leadership and oversight of multinational Phase I–IV clinical trials, including timelines, budgets, cross-functional teams, clinical sites, CROs and vendors.
REGULATORY & INSPECTION READINESS
Support with clinical trial start-up, CTIS and regulatory submissions, essential study documentation, TMF quality, audit preparation and inspection readiness.
About Dr. Katharina Schaub
Senior expertise for successful clinical trials
Dr. Schaub – Clinical Research Services provides independent, senior-level consulting and interim management services to pharmaceutical and biotechnology companies.
With more than 20 years of experience in international clinical trials, I support projects across Clinical Operations, Clinical Project Management, Global Clinical Trial Management, Study Start-up and Sponsor Oversight, as well as Clinical Outsourcing, CRO and Vendor Management, Contract and Budget Management, Regulatory Submissions and Inspection Readiness.
Therapeutic Area Expertise
Oncology, Immunology, Dermatology, CNS/Neurology, Rare Diseases and Cell & Gene Therapy
20+ Years
Clinical Research Experience
Since 2012
Independent Clinical Research Consultant