Samuel Anaya Cantu

Program Manager at emocha Health
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Contact Information
Location
US
Languages
  • Spanish Native or bilingual proficiency

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I have worked along Samuel for close to a year and it was an absolute pleasure. Not only did he excel at the core elements of his job - like contact tracing and enrollment specialist - but he was promoted from my peer to supervisor due to his hard work and dedication. He was always available to answer any questions that I would have and so patient and hard working. His willingness to learn and take on any new responsibility that comes his way is something to be desired in any professional.

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Credentials

  • Basic Life Support for Healthcare Providers (BLS)
    American Heart Association
    Dec, 2017
    - Sep, 2024
  • Advanced Cardiac Life Support (ACLS)
    American Heart Association
    Nov, 2013
    - Sep, 2024
  • Certified Clinical Medical Assistant (CCMA)
    National Healthcareer Association (NHA)
  • Certified Phlebotomy Technician (CPT)
    National Healthcareer Association (NHA)
  • Radiologic Technologist [Limited]
    Virginia Department of Health

Experience

    • United States
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Program Manager
      • Oct 2021 - Present

    • Assistant Project Manager
      • Oct 2020 - Present

    • Contact tracer and enrollment specialist
      • May 2020 - Oct 2020

      •Performed outreach via phone to enroll people into the emocha COVID-19 symptoms tracking app and provide COVID-19 information that complies with CDC guidelines•Assessed exposure details, symptoms and testing status of contacts and report to local health department.•Walked participants through onboarding onto the mobile app and help resolve any technical challenges.

    • United States
    • Medical Practices
    • 200 - 300 Employee
    • Certified Medical Assistant
      • Feb 2018 - May 2020

      •Performed a variety of clinical tasks, including taking patient medical history, providing wound care, casting, drawing blood, educating patients on use of medical equipment, providing post-surgical recovery instructions and care, performing foot/ankle x-rays, assisting physicians during in-office procedures etc. •Conducted administrative tasks such as maintaining electronic medical records, medical scribing, answering patient phone calls, and verifying patient insurance benefits. •Served as the team leader and coordinated with other medical assistants to ensure daily tasks were performed and completed in a timely fashion.

    • Medical Sub-Investigator
      • Mar 2014 - Dec 2014

      •Sub-Investigator in phase III/IV clinical trials. Ensured trials were conducted according to IRB approved protocol and complied with applicable regulations, including adherence to Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). •Screened, evaluated, and enrolled human subjects to clinical trials and obtained informed consent. •Ensured human subjects’ privacy, rights, and safety for the duration of a clinical trial. •Performed physical exams and monitored human subjects’ adherence to investigational drug. •Documented adverse effects and reported to Principal Investigator.

    • Mexico
    • Medical Practices
    • 1 - 100 Employee
    • General Physician
      • Mar 2014 - Nov 2014

      •Provided first aid and emergency care services to private companies and individuals. •Worked alongside paramedics to ensure patient safety during transportation to hospital and medical facilities •Provided first aid and emergency care services to private companies and individuals. •Worked alongside paramedics to ensure patient safety during transportation to hospital and medical facilities

    • Mexico
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Research Physician
      • Sep 2013 - Mar 2014

      •Recruited and enrolled individuals to bioequivalence clinical trials. Performed physical exams. Ensured the human subjects met the inclusion/exclusion. Explained risks to study subjects and obtained informed consent from them. •Attended staff meetings and contributed to the logistics, monitoring, and execution of trials. •Followed GCP/ICH guidelines, Standard Operating Procedures (SOPs), and good documentation practices (GDocP) for each protocol. •Supported clinical research assistants with reviewing and submitting documents to the IRB/IEC for approval. •Updated SOPs and manuals of the clinical department.

    • Government Administration
    • 1 - 100 Employee
    • General Physician
      • Jul 2012 - Sep 2013
    • Mexico
    • Hospitals and Health Care
    • 700 & Above Employee
    • General Physician
      • Jul 2012 - May 2013

Education

  • Universidad Autónoma de Nuevo León (School of Medicine)
    General Practitioner, MD, Medicine
    2004 - 2011

Community

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