Home Health Medical
Resume:
Sanford, FL *****
***********@*****.***
AMBER BROCKMEYER
OBJECTIVE Enthusiastic patient care provider seeks the opportunity to utilize extensive healthcare background to offer exceptional care to patients. SKILLS & ABILITIES ● Over fifteen years of experience in the field of medicine.
● Highly focused and proficient in medical terminology, management, reception and vendor marketing.
● Detail oriented, well organized multi-tasker.
● Excellent verbal and written communication skills.
● Dedicated, honest and dependable.
● over 5 years experience in clinical trials of phases I-III EXPERIENCE Oviedo Medical Research
July 2016-Present
Duties and responsibilities include,:
• Directs the conduct of clinical studies to ensure adherence to the research protocol and provides bimonthly updates to Principal Investigator on study progress.
• Screens patient records, databases, and physician referral summaries for identification of prospective candidates for research protocols.
• Interviews prospective subjects for participation in investigations and obtains informed consent.
• Participates in initiation visits/investigator’s meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor.
• Develops study working folders for assigned protocols to outline guidelines for protocol compliance and to assure complete source documentation.
• Educates human subjects for participation in investigations.
• Maintains consistent enrollment in protocols and provides monthly written documentation of screening/enrollment/follow-up activities.
• Draws, prepares, and ships laboratory samples for clinical trials.
• Maintains investigational drug/device dispensing accountability and shipping logs according to protocol guidelines.
• Performs EKGs and other procedures as directed by study protocol
• Instructs Principal Investigator on procedures and tests that need to be performed in compliance with the study protocol and advises Principal
• Completes phone logs for conversations with sponsors, patients, physicians, and coordinating organizations.
• Schedules follow-up visits for study patients in collaboration with Principal Investigator and provides source documentation for the activities conducted during these visits.
• Completes accurate and complete data entry into case report forms or pre-established computer programmed formats ensuring appropriate source documentation.
CLINICAL RESEARCH COORDINATOR, COMPASS RESEARCH/BIOCLINICA THE VILLAGES March 2014 – July 2016
Duties and responsibilities include,:
• Directs the conduct of clinical studies to ensure adherence to the research protocol and provides bimonthly updates to Principal Investigator on study progress.
• Screens patient records, databases, and physician referral summaries for identification of prospective candidates for research protocols.
• Interviews prospective subjects for participation in investigations and obtains informed consent.
• Participates in initiation visits/investigator’s meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor.
• Develops study working folders for assigned protocols to outline guidelines for protocol compliance and to assure complete source documentation.
• Educates human subjects for participation in investigations.
• Maintains consistent enrollment in protocols and provides monthly written documentation of screening/enrollment/follow-up activities.
• Draws, prepares, and ships laboratory samples for clinical trials.
• Maintains investigational drug/device dispensing accountability and shipping logs according to protocol guidelines.
• Performs EKGs and other procedures as directed by study protocol
• Instructs Principal Investigator on procedures and tests that need to be performed in compliance with the study protocol and advises Principal
• Completes phone logs for conversations with sponsors, patients, physicians, and coordinating organizations.
• Schedules follow-up visits for study patients in collaboration with Principal Investigator and provides source documentation for the activities conducted during these visits.
• Completes accurate and complete data entry into case report forms or pre-established computer programmed formats ensuring appropriate source documentation.
INSURANCE COORDINATOR AND PATIENT SERVICES REPRESENTATIVE, HCA/LAD IMAGING, DELTONA November 2009 – February 2016
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Provide professional and accurate service to schedule patient appointments, check-in and verify insurance eligibility. Update and maintain medical records in Meditech, utilizing proficiency in medical terminology and CPT/ICD-9 and ICD-10 codes. ADMINISTRATIVE SUPERVISOR, SANDLANDO SPRINGS ANIMAL HOSPITAL, LONGWOOD May 2003 – November 2009
Preform new employee training, Update and maintain medical charts in Avmark software system. Ensure steady workflow of daily procedures for both employees and doctors. Monitor and evaluate employee performance. Maintain and ensure adequate inventory for product displays. Process all rebate and reimbursement promotions. CERTIFIED CHIROPRACTIC ASSISTANT, DEMETREE CHIROPRACTIC GROUP, ALTAMONTE SPRINGS December 2008 – November 2009
Operate computerized medical equipment. Preform hydrotherapy, physiotherapy and electrotherapy to safeguard patient comfort and recovery. Assist with patient record updates and scheduling.
CERTIFIED HOME HEALTH AIDE, LIFE CARE HOME HEALTH, ALTAMONTE SPRINGS June 2001 – December 2008
Provide compassionate care and assistance for patients with limited mobility and terminal illness. Administer medication, track vitals and update medical records. EDUCATION SEMINOLE STATE COLLEGE – FLORIDA – ASSOCIATES DEGREE IN PRE NURSING Certified EMT
ACLS Provider
CPR Healthcare provider
GCP/IRB CERTIFICATIONS
IATA
REFERENCES AVAILABLE UPON REQUEST
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