Todd Cano

Todd Cano Email and Phone Number

Founding Principal and Chief Consultant @ Atlanta, GA, US
Atlanta, GA, US
Todd Cano's Location
Atlanta, Georgia, United States, United States
Todd Cano's Contact Details
About Todd Cano

Specialties: THERAPEUTIC EXPERIENCEAcute lymphoblastic leukemia (ALL)Acute Respiratory Syncytial Virus (pediatric device)Allergic RhinitisAllergy (pediatrics & adults) ALS Alzheimer’s Disease Anal fissures (Phases 1 & 3)Anaplastic large cell lymphoma (ALCL)Asthma (pediatrics & adults)Complicated Lower Urinary Tract Infections Crohn’s Disease Diffuse Large B cell lymphoma (DLBCL)Epilepsy (pediatrics) Hypertension Intra-abdominal infectionsMacular DegenerationMulti-Infarct DementiaMultiple myeloma Multiple Sclerosis Multiple Symptom Atrophy (MSA) Mycosis fungoidNon-Hodkin lymphoma (NHL)Optic NeuritisOral ContraceptivesOncology/Immuno-oncology (Cell Therapy)Parkinson’s Disease Peripheral T cell lymphomaPharmacokinetic and Safety StudiesPyelonephritis Renal cell carcinomaSickle Cell Disease (Gene Therapy)Sézary syndromeSocial PhobiaStroke Systemic Lupus (SLE) Arthritis Systemic Lupus (SLE) NephritisT cell leukemia/lymphoma (adult)Thalassemia (Gene Therapy)Transformed follicular lymphoma (FL)

Todd Cano's Current Company Details
Pharmaceutical Research Consultants

Pharmaceutical Research Consultants

Founding Principal and Chief Consultant
Atlanta, GA, US
Todd Cano Work Experience Details
  • Pharmaceutical Research Consultants
    Founding Principal And Chief Consultant
    Pharmaceutical Research Consultants
    Atlanta, Ga, Us
  • Pharmaceutical Research Consultants
    Founding Principal/Chief Consultant
    Pharmaceutical Research Consultants Sep 2006 - Present
    • 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
  • Ppd
    Project Manager
    Ppd Jan 2005 - Sep 2006
    • 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.
  • Ucb Pharma
    Clinical Trial Manager
    Ucb Pharma May 2003 - Dec 2004
    • 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
  • Covalent Group
    Senior Clinical Research Associate
    Covalent Group May 2002 - May 2003
    • 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
  • Teva Pharmaceuticals
    Senior Clinical Research Associate
    Teva Pharmaceuticals Oct 1999 - May 2002
    • 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
  • Quintiles
    Regional Clinical Research Associate
    Quintiles Feb 1996 - Oct 1999
    • 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
  • Quintiles Laboratories
    Project Manager Assistant
    Quintiles Laboratories 1996 - 1998

Todd Cano Skills

Clinical Trials Gcp Clinical Research Pharmaceutical Industry Clinical Development Protocol Cro Sop Neurology Oncology Fda Clinical Monitoring Good Clinical Practice Biotechnology Ctms Regulatory Submissions Training Edc Ind Clinical Data Management Medicine Regulatory Affairs Data Management Management Ich Gcp Electronic Data Capture Clinical Operations Software Documentation Asthma U.s. Food And Drug Administration Clinical Trial Management System Crf Design Human Resources Drug Development Allergy Pediatrics Access Testing Start Ups Regulatory Documentation Validation Hypertension Clinical Research Associates Therapeutic Areas Standard Operating Procedure Cro Management

Todd Cano Education Details

Frequently Asked Questions about Todd Cano

What company does Todd Cano work for?

Todd Cano works for Pharmaceutical Research Consultants

What is Todd Cano's role at the current company?

Todd Cano's current role is Founding Principal and Chief Consultant.

What is Todd Cano's email address?

Todd Cano's email address is to****@****hoo.com

What schools did Todd Cano attend?

Todd Cano attended Virginia Tech, Osbourn Park High School, Warrnambool High School.

What skills is Todd Cano known for?

Todd Cano has skills like Clinical Trials, Gcp, Clinical Research, Pharmaceutical Industry, Clinical Development, Protocol, Cro, Sop, Neurology, Oncology, Fda, Clinical Monitoring.

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