Ulrike Ferentzi

- Experience in coordinating a wide range of OR studies on a global level including rare diseases - Overall accountability for the execution of clinical operations strategy on the study - Maintains a positive and results-oriented work environment and meets timelines to drive projects to success - Demonstrates an extensive range of leadership and influencing capabilities to achieve the business objectives and goals for both Parexel and clients

- Performed site identification and selection activities as assigned - Conducted on-site and remote site management and monitoring activities (qualification, initiation and termination) - Conducted ethics submissions in Germany - Performed contract negotiations with Principle Investigators

- Conducted remote visits and site visits to study sites in Germany to boost patient recruitment - Developed and implemented relevant recruitment strategies for a global multi-center trial - Met recruitment targets in Germany and presented results to European team - Discussed relevant recruitment hurdles, referral systems and implementation of recruitment aids - Conducted spirometry training and continuous support to study sites

- Reviewed site selection-, site initiation-, and monitoring reports in an oncological study - Reviewed eCRF databases - Reviewed trial master files - Liaised with multi-disciplinary teams to implement a high-quality database

- Coordinated a German multi-central trial involving the close liaison with study centers, support in patient recruitment and monitoring of trial-relevant descriptive statistics - Conducted site initiation visits, monitoring visits and query management - Reviewed internal Standard Operating Procedures - Performed ethics submissions in Germany - Generated subject narratives for the study - Contributed to the development of a study protocol

- Co-authored internal standard operating procedures according to GCP guidelines - Liaised and collaborated with various departments to meet business needs - Developed, managed and archived trial master files - Liaised with inter-disciplinary teams

- Managed patients with cardiology and respiratory diseases - Managed patients requiring emergency interventions - Ascertained a high standard of care

- Managed large number of genetically distinct zooplankton (Brachionus plicatillis) population - Set up and conducted laboratory populations - Conducted genetic analyses (DNA extractions, PCRs, gel electrophoreses)

- Coordinated an international phase III trial in acute stroke under supervision of PI - Coordinated clinical activities on international multi-center trials - Implemented strategies to ensure timely subject recruitment - Conducted site initiation and monitoring visits within the UK - Liaised with ethics committees and research & development departments

- Managed a group of patients with a wide range of diseases including heart disease and respiratory diseases - Conducting emergency nursing interventions in majors, minors and resuscitation area - Assessed and prioritized a wide range of emergencies patients with heart and respiratory diseases by using the UK triage system - Taught and trained nursing students in advanced nursing procedures

General and Mental Health Nursing