Toni Homberg

• Professor of Research Methodology. Lead master classes and discussions, including complex topics, thesis advising, motivating and inspiring students

• Attend monthly meetings to discuss human and animal research protocols. Participate in approval decisions, give scientific recommendations, provide advice to researchers, verify adherence to good clinical practice, ethics standards and regulations

Provide medical expertise and collaborate during planning, initiating, execution, control and closing of clinical studies

Coordination of clinical studies, developing skills including

• Leadership, organization and communication during project work
• Project management
• Monitoring and protocol oversight
• Leading investigator meetings and protocol training
• Identification of medical, safety and staff issues for escalation, problem solving and risk mitigation
• Supporting a multitude of activities
• Ensuring safety of research subjects
• Ensuring quality
• Ensuring compliance with protocol, regulation, good clinical practice, ethical standards and procedures
• Ensuring traceability of source documents
• Managing patient recruitment, informed consent process and data entry
• Establishing relationships with stakeholders

Writing and reviewing clinical protocols, study reports and scientific articles, mastering

• Research and planning skills
• Design, validation and selection of clinical and safety outcome measures
• Creativity and rigor in study design
• Data analysis, presentation and discussion
• Prioritization of patient safety

Preparing presentations for conferences, staff training and external audiences

Standard operating procedures (SOPs) design

Scientific support to align business strategies

Work on multiple projects simultaneously

• Specialty medical consultation with the main objective of providing exceptional medical care. Comprehensive patient evaluation of patients with multiple comorbidities, with thorough examination, attention to detail and analytic approach for correct diagnosis, treatment, monitoring and prognosis. Use of standardized tools for diagnosis and follow-up. Communicating complex problems to patients in simple terms
• Communication with other specialists and patient referrals as needed
• Participation in continuous medical education (CME)
• Adherence to medical guidelines, regulations and good clinical practice

• Principal investigator for 2 protocols and associate investigator for 6 protocols
• Evaluated clinical study patients with immune-mediated, infectious, oncologic and chronic diseases. Comprehensive patient evaluation with thorough examination, attention to detail and analytic approach for correct diagnosis, treatment, monitoring and prognosis. Used study tools for measuring efficacy and safety parameters
• Collected data and followed protocols, operations manuals and case report form requirements
• Identified and reported adverse events
• Provided support to other investigators, data management personnel and pharmacovigilance personnel.
• Provided scientific advice
• Kept updated on study topics and clinical research topics
• Adhered to regulations, good clinical practice and clinical record keeping practices

• Prepared syllabus, classes and exams.
• Collaborated with department head to create dynamic, ongoing curriculum development.
• Used lectures, discussions and demonstrations to increase learning and classroom success.
• Provided counseling, taught study skills and study habits while motivating students.

• Prepared and taught classes in a creative and interactive way. Helped students develop study skills and habits, while keeping them motivated.