Tanja Pendl

Senior Clinical Research Associate equipped with extensive experience in clinical research of pharmaceutical and medical device industry in the conduct of phase I, II, III & IV of clinical studies in different stages:

Feasibility, Initiation, Monitoring and Close-out.

Enormous comprehension and excellent fast analytical problem-solving skills. Outstanding background of medicine and strong knowledge of coordination and supervision of regulatory/competent authorities, audits and inspection. Very diligent goal-oriented person with in-depth understanding/knowledge of quality management, medical standards,

compliance requirements and operational procedures.

10 years experience in Clinical Research

Master of science in clinical research