Cesar Ormeno, MD

Director Medical and Scientific Affairs at i3Research
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Contact Information
us****@****om
(386) 825-5501
Location
Escondido, California, United States, US

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5.0

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Dragana Bugarski Kirola

One can easily attain a tremendous amount of advise when transitioning to another field or career.The key is figuring out who is willing to give sound and educated advise. As a newly appointed medical director at I3 I was extremely appreciative when Cesar shared his experience in trying to help me prepare for an audit.Sharing his own anxiety from that time he offered both guidance and support that helped me breeze through the audit. His expertise and years of experience in anesthesiology and neurology in industry on challenging trials such as new treatments of pain brought great satisfaction to clients as Cesar pays attention to the detail and addresses concerns with great clinical judgment and professional dedication. Despite his years of experience Cesar's has a non-assuming, gentle and respectful approach to his junior colleagues retaining the attitude that he too can learn from them, a virtue less frequently seen these days.His valuable consultation and expertise have allowed many sponsors to move forward with their projects. I remain grateful for his outstanding advise and support as a peer. It is my pleasure to recommend him to any company and sponsor who seeks experts with knowledge, professional dedication and more importantly , integrity.

Alex De Windt, MD

It is with pride that I have the pleasure to recommend Dr. Cesar Ormeño. During my tenure at i3 Research, Dr. Ormeño and I collaborated in different projects. He was known for his capacity, experience and dedication in the field of Pharmaceutical Medicine. An anesthesiologist by training, he successfully managed and advice the medical safety of many projects. Definitely, Dr. Ormeño is an asset to any institution that chooses to use his vast knowledge and expertise. Alex V. De Windt, MD Director, Medical Affairs Icon Clinical Research.

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Experience

    • Pharmaceutical Manufacturing
    • 200 - 300 Employee
    • Director Medical and Scientific Affairs
      • Nov 2004 - Present

      • Designated physician responsible for coordinating all activities related to the medical monitoring of a trial protocol. • Oversees overall reliability and validity of medical data generated• Responsible for coordinating activities of the medical team assigned to the project. • The responsibilities include:o carry out all medical monitor/advisor activities according to the sponsor established requirements and contract specifications, o reviewing of contracto draft versions of the protocolo all medical and safety informationo determine whether the subject medical information protocol, Investigator Drug Brochure or other available relevant safety information on the investigational product(s) under studyo will review the Investigator Drug Brochure with particular attention to those aspects relating to safety data involving human subjectso perform a periodic review of available literature on the therapeutic modality under investigationo aware of all relevant clinical research guidelines involving the therapeutic indication (ICH/GCP, FDA guideline, Declaration of Helsinki). Show less

    • Medical Advisor
      • Jul 2001 - Nov 2004

      Medical Advisor • Member of the Medical Affairs group, liaison between sponsor and investigators• Responsible for site management including medical monitoring; review of Inclusion/Exclusion criteria• Review of laboratory reports and electrocardiograms. • Ensuring that the medical data generated from the project is valid and reliable. • Provides medical and scientific input into the design of clinical protocols, including objectives, patient populations and procedures for evaluating safety and efficacy. Show less

    • Senior Clinical Research Associate
      • Jun 1999 - Jun 2001

      Member of clinical operations team and liaison between sponsorsand investigators; responsible for site management, including Pre- study Site Qualification Visit, Study Site Initiation, Monitoring and Closeout, Clinical reports and completion of all phases of clinical trials. Also, responsible for training and mentoring new CRAs.

Education

  • Universidad Nacional Mayor de San Marcos
    1970 - 1979

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