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CCRC

Location:
San Antonio, TX, 78244
Posted:
December 30, 2011

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Resume:

Professional Summary

Research Related: Prepared regulatory documents and budgeting issues for protocols, prepared research protocols for IRB approval, coordinated study implementation including recruitment, screening, and enrollment, preparing source documentation, completion of case report forms and EDC forms, drug compliance with GCP. Patient assessment, teaching and training to personnel regarding current studies.

Professional Experience:

Research and Development Coordinator:

MP Consultants Feb 2011- Present

• Negotiated and executed lease for facility with Attorneys

• Hired staff

• Negotiated and executed contracts with ALL vendors- Surgical Equipment and Supplies

• Hired Staff

• Implemented/ Trained staff on facility policy and procedures

• Implemented and Confirmed that all equipment, documents, training, licensing were in accordance with specific guidelines.

• Coordinated Grand Opening

• Prepared all documents for LT Physicians under TMA and TMLT

• Negotiated and executed staff medical benefits with insurance company

• Implemented research at the facility- Prepared/Negotiated contracts with Pharma Companies, prepared all regulatory documents for FDA review, and trained staff.

• Trained staff on specific protocols

• Implemented facility Laboratory, including completion of CLIA application.

• Generated SOP’s for facility

• Coordinate and maintain all hours including vacation/holiday for over 10 employees.

• Reputation for dependability, honesty, dedication and enthusiasm. Provide premium service to both internal and external customers.

• Demonstrated ability to quickly learn organizational processes, workflows, policies and procedures of various companies.

• Expert interpersonal and communication skills -- known for tactful handling of sensitive, confidential issues; ability to resolve customer complaints; and timely completion of polished, executive-level

Jeff Davis Law Firm:

Medical Case Manager Oct 2010- Feb 2011

• Review all client medical records for 3 Attorneys

• Prepared all documents/medical records for court and judge

• Updated all medical records for clients

• Scheduled Dr. appointments for clients

• Submitted required completed documents to SSA.

• Performed initial intake for Attorneys to determine/prove verbalized diagnosis.

Clinical Research Coordinator:

Covenant Clinical Research May 2009- Dec 2009

• Order lab and X-rays

• Prioritize patient daily care according to acuity and scheduled patient procedures

• Assist patients with A.M. care,take vital signs,prep for procedures, obtain and process specimens

• Perform preventative maintenance on emergency equipment

• Assist with patient and family diabetes education

• Perform sterile and non-sterile dressing changes

• Perform EKGs

• Utilize PC to enter and retrieve patient data

• Answer multi-line phone , operate fax and copy machine

• Prepare patient charts for interim monitoring visits

• Perform internal QA on clinic charts

Clinical Research Coordinator:

Peripheral Vascular Associates April 2008- May 2009

• Order lab and X-rays

• Prioritize patient daily care according to acuity and scheduled patient procedures

• Assist patients with A.M. care, take vital signs, prep for procedures, obtain and process specimens for shipping.

• Perform preventative maintenance on emergency equipment

• Assist with patient and family diabetes education

• Perform sterile and non-sterile dressing changes

• Perform EKGs

• Utilize PC to enter and retrieve patient data

• Answer multi-line phone , operate fax and copy machine

• Prepare patient charts for interim monitoring visits

• Perform internal QA audits

• Assist in cath lab holding; Consent patients prior to procedures, assist with IV placement, complete patient care

• Generate flyers for physicians/patient retention and recruitment

Alamo Area Heart Rhythm Consultants June 2010- Oct 2010

Receptionist/ Medical Assistant

• Check all patients

• Schedule appointments/surgeries

• Verify Insurance

• Obtain ALL pre-certifications

• Assist the physician when needed

• Phone triage

• Call in prescriptions/refills

• Answer multi phone lines

• Perform ALL Medical Assistant duties

Lead Clinical Research Coordinator

WellMed Clinical Research February 2006-April 2008

• Order lab and X-rays

• Prioritize patient daily care according to acuity and scheduled patient procedures

• Assist patients with A.M. care, take vital signs, prep for procedures, obtain and process specimens for shipping.

• Perform preventative maintenance on emergency equipment

• Assist with patient and family diabetes education

• Perform sterile and non-sterile dressing changes

• Perform EKGs

• Utilize PC to enter and retrieve patient data

• Answer multi-line phone , operate fax and copy machine

• Prepare patient charts for interim monitoring visits

• Perform internal QA audits

• Generate flyers for physicians/patient retention and recruitment

• Perform weekly staff meeting (incl :physicians)

• Cross train all staff on all protocols

• Generate recruitment plans for Director and Pharmaceutical companies

• Maintain patient payments

• Recruit for new clinical trials

Clinical Research Coordinator

Pro-Research Group March 2000- October 2005

• Order lab and X-rays

• Prioritize patient daily care according to acuity and scheduled patient procedures

• Assist patients with A.M. care, take vital signs, prep for procedures, obtain and process specimens for shipping.

• Perform preventative maintenance on emergency equipment

• Assist with patient and family diabetes education

• Perform sterile and non-sterile dressing changes

• Perform EKGs

• Utilize PC to enter and retrieve patient data

• Answer multi-line phone , operate fax and copy machine

• Prepare patient charts for interim monitoring visits

• Perform internal QA audits

• Generate flyers for physicians/patient retention and recruitment

• Perform weekly staff meeting (incl :physicians)

• Cross train all staff on all protocols

• Generate recruitment plans for Director and Pharmaceutical companies

• Maintain patient payments

• Recruit for new clinical trials

SKILLS

Skill Name Skill Level Last Used/Experience

MS Office Suite Expert Currently used/10 years

Spreadsheets Expert Currently used/7 years

Filing & Records Management Expert Currently used/10 years

Front-Desk & Phone Reception Expert Currently used/10 years

Customer Service Expert Currently used/7 years

Payroll Intermediate 1 year ago/1 years

Office Management Intermediate 1 year ago/1 year

Calendaring/Scheduling/Meeting Planning Expert Currently used/10 years

Administrative & Executive Support Expert Currently used/4 years

Word Processing/Typing (50 WPM) Expert Currently used/10 years

Certification:

IATA- Transportation of Dangerous Goods- April 2004

ACRP- Certified Clinical Research Coordinator- 2005

Education:

Northwest Vista College- Allied Health

Clinical Trial Experience:

Phase II- IV

Device Trials

NIH

Research Training:

ABI with Toe Pressures

Endothelial Testing

Pulmonary Function Testing

EKG

INR Testing

Glucose Monitoring

Treadmill/ Garner Protocol

TCPO2

24 Holter Monitoring/AMBP

INR Testing

Glucose Monitoring

Treadmill/ Garner Protocol

TCPO2

24 Holter Monitoring/AMBP

Therapeutic Areas

Peripheral Vascular Disease GERD

Critical Limb Ischemia Gastro paresis

Diabetes Mellitus- Type 1 and II Pneumonia

Hypertension GOUT

Hyperlipidemia Genital Herpes

Osteoarthritis/ Rheumatoid Erectile Dysfunction

COPD Chronic/Acute Sinusitis

Asthma Diabetic Foot Ulcer

Allergic Rhinitis Gastric Ulcers

Bronchitis Venus Ulcers

Pedi- Hypertension



Contact this candidate