Experience

Yale Cancer Center

• United States
• Hospitals and Health Care
• 1 - 100 Employee

• Clinical Research Coordinator

  • Jun 2022 - Present

  • Administratively and clinically manage several clinical trials• Adhere to research standard of procedures• Adhere to good clinical practices and the study protocols• Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials• Discuss study protocols with patients and verify the informed consent documentation• Provide patient with written communication of their participation (i.e. copy of the signed informed consent)• Ensure patient’s referring physician receives notification of patient’s participation in studies as requested by the patient• Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study• Dispense study medication in a professional and accountable manner following protocol requirements• oversees scheduling of all patient research visits and procedures consistent with protocol requirements• Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy• Administer questionnaires/diaries per protocol• Ensure that non-serious and serious adverse events are properly documented and reported• Screen all laboratory results when received and follow protocol procedure regarding abnormal results• Ensure all laboratory results are given to appropriate doctors for review of clinical significance, then file results in the patient study binder• Submit patient reimbursement requests at the conclusion of patient’s participation in protocol• Ensure the filing and maintenance of all regulatory documents• Schedule monitor visits and set up for monitoring visits prior to monitor’s arrival



Montefiore Health System

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Clinical Research Coordinator

  • May 2020 - Aug 2022

  • Administratively and clinically manage more than one clinical trial• Adhere to research standard of procedures• Adhere to good clinical practices and the study protocols• Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials• Discuss study protocols with patients and verify the informed consent documentation• Provide patient with written communication of their participation (i.e. copy of the signed informed consent)• Ensure patient’s referring physician receives notification of patient’s participation in studies as requested by the patient• Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study• Dispense study medication in a professional and accountable manner following protocol requirements• Collect, process, and ship blood/urine specimens at scheduled patient visits• Perform ECGs, Phlebotomy and obtain vital signs of patients• Schedule all patient research visits and procedures consistent with protocol requirements• Complete and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy• Administer questionnaires/diaries per protocol• Ensure that non-serious and serious adverse events are properly documented and reported• Screen all laboratory results when received and follow protocol procedure regarding abnormal results• Ensure all laboratory results are given to appropriate doctors for review of clinical significance, then file results in the patient study binder• Submit patient reimbursement requests at the conclusion of patient’s participation in protocol• Ensure the filing and maintenance of all regulatory documents• Schedule monitor visits and set up for monitoring visits prior to monitor’s arrival

• Patient Care Technician

  • Nov 2012 - May 2020

  • Assisted 30+ patients per day and post examination protocol• Measured and recorded vital signs.• Urinalysis tests.• Assisted the Doctor during GYN procedures.• Prepared and sent out specimens for laboratory testing.• Contacted Hospitals, clinics or diagnostic Labs to obtain the tests results.



Weill Cornell Medicine

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Clinical Technician

  • Feb 2011 - Nov 2012

  • Assisted 30+ patients per day and post examination protocol• Measured and recorded vital signs.• Performed Phlebotomy daily.• Assisted the Doctors with Co- culture biopsy’s, Saline Ultrasound• Assisted the Doctor during GYN procedures.• Prepared and sent out specimens for laboratory testing.• Verify patients’ insurances.• Assists patients with recovery after procedures • Assisted 30+ patients per day and post examination protocol• Measured and recorded vital signs.• Performed Phlebotomy daily.• Assisted the Doctors with Co- culture biopsy’s, Saline Ultrasound• Assisted the Doctor during GYN procedures.• Prepared and sent out specimens for laboratory testing.• Verify patients’ insurances.• Assists patients with recovery after procedures