Dr. Martin Waldherr

Responsibilities included consultations for clinical research issues and conducting of clinical trials, especially Monitoring for international CROs, Pharma- and Biotech Companies, but also the position as a Country Manager for Austria on behalf of international CROs and the development of strategies for making the Austrian affiliate a very prosperous one, Contract Negotiations, Medical Liaison and performing Feasibility Assessments.

Responsibilities included working closely with the Director of Project Management, leading teams and CROs to ensure all aspects of the project are on target (recruitment of investigators, negotiation of study budgets, ethics submissions, investigator contracts, patient recruitment and study deliverables), assuring training for the CRAs.

Responsibilities included clinical trials coordination to oversee the conduct of a study to ensure the quality and integrity of the data produced at investigator sites, which includes responsibility for all project activities within Clinical Operations, liaising with Project Management, other functional leads and the sponsor.

Responsibilities included clinical trials monitoring in accordance with the ICH Guideline and the current monitor guidelines and SOPs including identifying sites.

Responsibilities included conducting of clinical trials, revising protocols and preparing financial agreements.

Responsibilities included conducting of clinical trials.

Responsibilities included development of new bacterial strains for the biotechnological industry.

PhD, Microbiology and Genetics