Phlebotomist ll

miasharpe**@Mia gmail.Sharpe com Orlando, FL

PROFESSIONAL SUMMARY

Highly skilled Medical Assitant/ Phlebotomist with extensive Leadership and clinical experience.

WORK HISTORY

Clinical research Coordinator at CareAccess

01/2023 - 04/2023 (4 months)

Assisting in screening patients, obtaining Informed Consent from the patient, maintaining patient

charts organized

Formulate observations, note results in CRF eCRF Source documentation systems.

Draw inferences about trial assessments and report on conclusions. Prepare lab specimens for delivery to reference laboratory. Ensure proper handling of specimens according to in house reference laboratory protocols.

Ensure lab specimens are appropriately labeled with proper test(s) ordered, correct accession

number, tube type, etc. required to perform necessary procedures. Provide research support by preparing trial assessments, analyzing data, perform comparative

analyses from former experimental data.

Notify lab processor of any issues with orders and or lab specimens. Develop research papers for publication based on experimental results and analysis.

Clinical Research Coordinator at APG Research, LLC 02/2022 - 11/2022 (1 year)

Assisting in screening patients, obtaining Informed Consent from the patient, maintaining patient

charts organized

Formulate observations, note results in CRF eCRF Source documentation systems.

Draw inferences about trial assessments and report on conclusions. Prepare lab specimens for delivery to reference laboratory. Ensure proper handling of specimens according to in house reference laboratory protocols.

Ensure lab specimens are appropriately labeled with proper test(s) ordered, correct accession

number, tube type, etc. required to perform necessary procedures. Provide research support by preparing trial assessments, analyzing data, perform comparative

analyses from former experimental data.

Notify lab processor of any issues with orders and or lab specimens. Develop research papers for publication based on experimental results and analysis.

Clinical Research Coordinator at SIH Research

06/2019 - 01/2022 (3 years)

Obtained Informed Consent Forms, enrolled subjects into clinical trials where eligible.

Scheduled obtained patient information including medical history, EKG information and any

biological samples as specified in each respective protocol. Formulated, prepared, and maintained source documentation while preparing patients for specific

trial assessments as specified per the protocol.

Assist Principal Investigator with patient examination and administration of investigational

product.

Collected and processed patient specimens for select diagnostic tests. Serves as liaison between physician and other business affiliates. Managed practice finances and inventory of office materials equipment Clinical Research Coordinator RMA at Rheumatology Associates of Central Florida

09/2016 - 05/2019 (3 years)

Protocol evaluation

Clinical trial preparation involving the planning, assembling, and instruction of the trial team.

Communicating with relevant authorities.

Recruitment and coordination of the trial subjects. Covering informed consent, screening, and inclusion exclusion criteria of the subjects.

Adhering to safety and compliance issues.

Communication with sponsor and authorities

Visit coordination, sampling, time management and product accountability. Data collection and management, collection of source documents, using and developing Case Report

Forms (CRF s), filling and archiving, resolving queries, managing, and monitoring visits, and

registration and management of Adverse Events (AEs) Phlebotomy performed according to study protocol and requirements. ECG

Preparation of blood samples for shipment to appropriate lab Vital cardinal signs, obtaining medical histories, assisting Principal Investigator Sub Investigator with physical exams or study specific procedures.

Answering phone calls from enrolled subjects, doctor offices and future subjects

Fax documentation to appropriate entity regarding studies and subjects. Clinical Research Assistant RMA at Florida Hospital Translational Research Institute for Metabolism and Diabetes

06/2015 - 09/2016 (1 year)

Processing and preparation of lab specimens.

Phlebotomy and patient care.

Subject observation

Review of study procedures and subject education.

Assisting physicians with trial procedures.

ECG and Vital signs

Collection and processing of twenty four hour urine collection IVs Team communication training of new staff

Clinical Research Assistant RMA at Compass Research 09/2010 - 05/2015 (5 years)

Lab Led or Phase I and Phase II studies.

Collection, Processing and Shipping of Lab specimens ECK and Vital and Cardinal Signs and IVs

Collection and processing of twenty four hour urine collection samples Patient Care

Assisting physician and nurses with trial procedures according to protocol Data collection

Assist with new staff training.

Clinical Research Assistant RMA at Florida Clinical Research Center 04/2008 - 09/2010 (2 years)

Lead Medical Assistant

Lab Coordinator

Updating and maintain subject enrollment logs.

Answering phone calls Maintain Subject Payment logs. ECG and IVs

Collections, Processing and Shipping of lab specimens including twenty four hour urine

collections.

Patient care and Education

EDUCATION

Graduated 1970

IATA Certificate

Graduated 1970

NIH GCH Training

Graduated 1970

CRP Certification

Graduated 1970

IV Certification

Graduated 1970

R.M.A

SKILLS

coordinating, 0 year

leadership, 0 year

problem solving, 0 year

appointment scheduling, 0 year

pharmaceuticals, 30 years

LANGUAGES

English, Moderate

SOCIAL NETWORKS

Facebook, https://**************@*****.***

Linkedin, https://www.linkedin.com/in/nancy-barkley-b2600a7/ ABOUT ME

I served in the military

I have a drivers license

I have management experience

I have a security clearance

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