1. CURRICULUM VITAE
Kory E. Winkler, BS
7502 State Road, Suite 4400
Cincinnati, OH 45255
Telephone: (513) 281-3868
Fax: (513) 281-1370
4760 Red Bank Expressway, Suite 217
Cincinnati, OH 45227
Telephone: (513) 721-3868
Fax: (513) 639-7343
Corporate:
CTI Clinical Trial and Consulting Services
10123 Alliance Road
Blue Ash,OH 45242
Phone (513) 598-9290
Fax (513) 598-3426
Email: kwinkler@ctifacts.com
Professional Experience
2011- Present CTI Clinical ResearchCenter (CTI CRC)
Senior Clinical Research Coordinator (2011-Present)
 Maintain a high level of knowledge and understanding of assigned protocols, including
all protocol and training requirements: obtaining informed consent, adhering to study visit
schedules, tests, procedures, laboratory, and drug accountability requirements.
 Act as a technical resource and assist with training and mentoring to less experienced
research coordinators; answer questions, provide work samples or other assistance and
support as needed.
 Recruit study participants for studies. Work with the Marketing/Recruitment Department
with developing advertising strategy and materials and interview questionnaires.
 Meet with potential study participants to perform informed consent process and collect
medical history. Refer patients to other professionals as needed. Make calls to
participants to relate acceptance and next steps.
 Create source templates for study documentation, complete case report forms, and
other study specific documents.
 Coordinate and conduct patient care visits and assure all procedures are conducted in
compliance with the clinical protocol. Maintain patient safety, assess feedback from
patient and refer to investigators or other professionals as needed.
 Interact with Investigators or study sponsors as needed to assure study participants
receive appropriate medical evaluation and care when needed.
 Interact with sponsor Clinical Research Associate to facilitate the sponsor monitoring
and database clean-up process.
 Attend sponsor Investigator/Study Coordinator meetings as needed for assigned
protocols.

CV- Kory Winkler, BS

2. Professional Experience Continued
 Conduct clinical research in compliance with all applicable regulations. Comply with
Good Clinical Practices (GCPs).
2006-2011 Community Research
Clinical Research Coordinator II (2008-2011)
 Maintain knowledge and understanding of assigned protocols, including all protocol
requirements for patient visits, obtaining informed consent, patient visit schedules, tests,
procedures, laboratory information, and drug accountability requirements.
 Recruit study participants for studies. Work with the Marketing/Recruitment Department
to develop advertising strategies, materials, and interview questionnaires.
 Meet with potential study participants to perform informed consent process, and collect
medical history. Refer patients to other professionals as needed.
 Make final pre-study call to participants to relate acceptance and next steps.
 Create source templates for study documentation, complete case report forms and other
study specific documents
 Coordinate and conduct patient care visits and assure all procedures are conducted in
compliance with the clinical protocol. Maintain patient safety.
 Interact with investigators or study sponsors as needed to assure study participants
receive appropriate medical evaluation and care when needed.
 Interact with sponsor Clinical Research Associate to facilitate the sponsor monitoring
and database clean-up process.
 Attend sponsor Investigator/Study Coordinator meetings as needed for assigned
protocols.
 Conduct clinical research in compliance with all applicable regulations. Comply with
Good Clinical Practices (GCP’s)
Clinical Research Coordinator I (2006-2008)
 Maintain knowledge and understanding of assigned protocols, including all protocol
requirements for patient visits, obtaining informed consent, patient visit schedules, tests,
procedures, laboratory information, and drug accountability requirements.
 Recruit study participants for studies. Work with the Marketing/Recruitment Department
to develop advertising strategies, materials, and interview questionnaires.
 Meet with potential study participants to perform informed consent process, and collect
medical history. Refer patients to other professionals as needed.
 Make final pre-study call to participants to relate acceptance and next steps.
 Create source templates for study documentation, complete case report forms and other
study specific documents
 Coordinate and conduct patient care visits and assure all procedures are conducted in
compliance with the clinical protocol. Maintain patient safety.
CV- Kory Winkler, BS
Professional Experience Continued

3.  Interact with investigators or study sponsors as needed to assure study participants
receive appropriate medical evaluation and care when needed.
 Interact with sponsor Clinical Research Associate to facilitate the sponsor monitoring
and database clean-up process.
 Attend sponsor Investigator/Study Coordinator meetings as needed for assigned
protocols.
 Conduct clinical research in compliance with all applicable regulations. Comply with
Good Clinical Practices (GCPs).
2001-2006 Battelle Memorial Institute
Senior Safety Pharmacology Technician (2004-2006)
 Maintained knowledge and understanding of assigned protocols, including all protocol
requirements for tests, procedures, laboratory information, and drug accountability
requirements.
 Created source templates for study documentation, completed case report forms and
other study specific documents
 Coordinated and conducted animal care and assured all procedures were conducted in
compliance with the clinical protocol. Maintained animal safety.
 Interacted with sponsor Clinical Research Associates to facilitate the sponsor monitoring
and database clean-up process.
 Attended sponsor meetings as needed for assigned protocols.
 Conducted pharmaceutical research in compliance with all applicable regulations.
Comply with Good Laboratory Practices (GLPs).
 Completed Animal Husbandry and Enriched Animals daily
Senior Toxicology Technician (2003-2004)
 Maintained knowledge and understanding of assigned protocols, including all protocol
requirements for tests, procedures, laboratory information, and drug accountability
requirements.
 Provided support to veterinary staff when conducting PE/Animal Check Ups
 Completed Animal Husbandry and Enriched Animals daily
 Coordinated laboratory technician visits
 Assured all procedures were conducted in compliance with the clinical protocol
 Centrifuged samples and placed in appropriate vessels or vials properly per lab manual.
 Collected vital signs
 Collected electrocardiograms
 Maintained a safe and clean lab in accordance with Good Laboratory Practices and OSHA.
CV- Kory Winkler, BS
Professional Experience Continued

4. Pharmaceutical product Development Animal Technician (2001-2003)
 Maintained knowledge and understanding of assigned protocols, including all protocol
requirements for tests, procedures, laboratory information, and drug accountability
requirements.
 Completed Animal Husbandry and Enriched Animals daily
Therapeutic Experience
 Sleep Disorders
 Dermatology
 Rare Disease
 Musculoskeletal
 Endocrinology
 Moist and Dry Heat Products
 Phase 1 General Healthy
 Vaccine
 Neurology
 Psychology
 Rheumatology
 Pulmonology/Respiratory Disease
 Cardiology
 Traumatic brain Injury
Education Background
Bachelor of Science (Biology)
Heidelberg University