Todd Cano Email & Phone Number

Atlanta, Ga, Us

• Work as a consultant on various clinical research projects as a Project Manager, Program Director, or Clinical Research Associate.• Provide assistance on writing protocols, selecting study sites, contract and budget negotiations, training of study and site staff, global management of research study, monitoring of subjects at study sites, closing down of study sites and study, archival of study records, submission of IND applications

• Successfully managed two Global, Full-service clinical trials according to timelines and quality standards. • Coordinated activities of all functional departments and vendors involved in the projects. Worked with teams and management to develop plans/guidelines for project implementation using PPD tools. Monitored and analyzed project status to ensure successful completion of project parameters, milestones, and timetables (i.e, regulatory document, research agreement, site payments, interim monitoring, CRF retrieval, CRF data entry, etc.). Ensured teams entered and updated internal tracking tools. Worked with teams to identify potential risks, developed contingency plans as warranted.• Supervised and mentored CRAs and provided guidance to newly hired Project Managers and Clinical Team Managers.

• Managed the United States and Canadian regions of an in-patient Global Pediatric (Ages 1 Month to less than 4 years old) Epilepsy Clinical Trial using Video-EEG for patients with Refractory Partial Onset Seizures• Performed co-monitoring visits to ensure CRA and investigator adherence to SOPs, ICH guidelines, GCP, and that the data was complete, accurate and consistent• Prepared project timelines and ensured adherence by the study team• Coordinated writing of clinical trial documents, such as informed consent templates, protocol amendments, monitoring guidelines, case report forms (CRF) and CRF completion guidelines• Oversaw the identification, evaluation, selection, initiation, and monitoring of clinical investigators in the US and Canadian regions• Provided updates to a Global Clinical Project Manager and ensured that IMPACT tracking databases are consistently updated

• Responsible for monitoring several Hypertension studies • Managed the CRAs assigned on two Hypertension studies and ensured monitoring visits were completed within the monitoring guidelines set forth for the study• Reviewed trip reports, letters, and telephone call reports written by CRAs for accuracy and thoroughness• Ensured outstanding issues noted by CRAs received appropriate follow-up and resolution

• Responsible for monitoring Primary Progressive Multiple Sclerosis study• Verified patients met inclusion criteria for entry into Primary Progressive and Relapsing-Remitting Multiple Sclerosis studies, through the review of medical charts including Lumbar Puncture results, Cervical MRIs, Brain MRIs, documentation of disease course, B12 results and other testing used to confirm diagnosis • Cross-trained to assist as needed with Parkinson’s Disease studies• Averaged 95% travel, monitoring up to 15 sites, in 10 states with a total of over 250 patients• Trained site staff on Good Clinical Practices, FDA Regulations, and Protocol requirements• Conducted a thorough review of the Regulatory documentation for completeness• Verified patients maintained compliance with study medication as specified by the protocol

• Responsible for monitoring multi-infarct dementia and Alzheimer’s studies• Conducted site selection, site initiation, interim monitoring and closeout visits• Co-monitored on stroke, Alzheimer’s disease, social phobia and ALS studies• Assisted clinical project teams with in-house monitoring activities and locking of databases• Participated in the development of edit specifications for data• Ensured adherence to Good Clinical Practices, FDA Regulations, investigator integrity and compliance with protocol• Verified accuracy and accountability of regulatory documentation and patient’s compliance with study medications• Performed an in-house review of case report forms (CRFs) for completion, accuracy and consistency, generated data clarification requests, verified corrected CRF accuracy and sent the CRFs to data management for entry

Education record

Education record

Education record