Annette Burkhardt

Über mich

Dynamic consultant, manager and clinical research associate with specialised expertise leading and supporting pharmaceutical and oncology studies and managing all needed documentation.
Advanced expertise in independent study site start-up and monitoring, including on-site visits, certified translations German-English-German, reporting and follow-up.
Strong background in Good Clinical Practice, with expertise spanning clinical study audits, management and monitoring, post-market surveillance, quality management and compliance.
Demonstrated technical proficiency in use of clinical trial management systems and databases proficient in developing new procedures to ensure data integrity and accessibility.