Marisol Angel Corrales
Redding
Summary
I am seeking a position as an Administrator Secretary III (DSA). I can answer phones, transfer calls, and take messages. I have experience communicating with customers and staff members, collecting information needed by the office staff, inputting data into computers, typing, and filing. I also handle scheduling patients for appointments and ordering office supplies.
Professional administrative expert with broad experience in managing office operations, scheduling, and correspondence. Strong focus on team collaboration and achieving outcomes. Highly adaptable, reliable, and skilled in organizing, multitasking, and maintaining confidentiality. Known for effective communication and problem-solving abilities, contributing to a productive work environment.
Overview
22
22
years of professional experience
Work History
Phlebotomist
Quest Diagnostics
09.2019
- Accessing patients, and drawing all samples for testing, i.e. blood samples, urine, stool, and sputum. Scheduling appointments, answering phones, and processing insurance information.
Clinical Research Coordinator
Paradigm Clinical Research
10.2019 - Current
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
- CRC manages and conducts the day-to-day activities of a clinical trial. In general, the CRC ensures that the clinical study adheres to the protocol, applicable regulations, FDA audits, and Good Clinical Practice. The CRC is responsible for data entry, recruiting, patient care, monitoring vital signs, registering participants, setting them up with payment cards, and following protocols.
Phlebotomist
St. Elizabeth Hospital
02.2013 - 06.2013
- Accessing patients, and drawing all samples for testing, i.e. blood samples, urine, stool, and sputum. Scheduling appointments, answering phones, and processing insurance information.
Phlebotomist
Labcorp
02.2003 - 01.2013
- I was drawing blood samples from patients, including infants and trauma patients from the E.R. Processing, answering phones, and plating cultures.
Education
High School Diploma -
Alvord High School
01.1997
CNA Certification - undefined
Shasta College
01.2002
Skills
- Bilingual (English and Spanish)
- Excellent Customer service
- Ability to communicate orally and in writing
- Exceptional multitasking ability
- Record preparation
- Scheduling and calendar management
- Correspondence preparation
- Database entry
- Database administration
- File organization
Timeline
Clinical Research Coordinator
Paradigm Clinical Research
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Clinical Research Coordinator (CRC)
PARADIGM CLINICAL RESEARCH- REDDING CA
10.2019 - Current
Phlebotomist
Quest Diagnostics
09.2019
Phlebotomist
St. Elizabeth Hospital
02.2013 - 06.2013
Phlebotomist
Labcorp
02.2003 - 01.2013
CNA Certification - undefined
Shasta College
High School Diploma -
Alvord High School
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