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  Home  >   Pharmaceutical  >   Research

Clinical Research Associate Resume
Clinical Research Associate
  
St. Davids, PA

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OBJECTIVE
My objective is to gain employment as a Clinical Research Associate in a company that promotes both personal and professional growth.
 
RELOCATE
PA


*****Partial listing of resume.******* ******Please sign up for full access.****** ; Participate with in-house pre-audit committee.

 Maintain and complete all required CRF and source documents.

 Receive, dispense, and track all required study medication.

 Track all required regulatory documents, study equipment, and CRF’s.

 Work with CRA’s, FDA, and sponsor representatives to resolve study related issues, monitoring visits, and audits.

 Monitor FDA and GCP compliance for all assigned clinical trials.

2000-2003 Controlled Environmental Services Philadelphia,PA

Project Supervisor

 Supervised demolition and hazardous material removal projects.

 Recruited personnel, submitted payroll and cost reports, and negotiated the sale of salvaged materials.

 Conducted weekly progress meetings with the assigned Project manager.

 Performed and maintained OSHA and Union guidelines of operation.





1997-2001 Fairmount Behavioral Hospital Roxborough, PA

Patient Care Technician

 Conducted group and individual counseling sessions.

 Worked with treatment teams to develop individualized care plans.

 Provided daily progress reports for patients medical records.

 Performed medication/treatment orientation with patients and their family.



1991-1995 2nd Ranger Bn. Ft. Lewis, WA

Special Operations Team Leader

• Conducted training and equipment orientation classes.

• Submitted personnel assessment and training reports.

• Developed training and operations S.O.P.’s.







EDUCATION

2003-2005 PCOM Philadelphia, PA

 M.S., Master’s in Biomedical Sciences

1999-2003 Drexel University Philadelphia, PA

 B.S., Allied Physical Sciences

 Member of Golden Key National Honor Society





RESEARCH EXPERIENCE

In addition to the six years of research experience gained during my academic pursuits, please see the attached CV for my professional experience.



















DEREK LAMONDE, CRC

CURRICULUM VITAE





EXPERIENCE:



2004 – Present CNS Research Institute, P.C.

130 White Horse Pike

Clementon, NJ 08021

Clinical Research Coordinator



2000 – 2004 Controlled Environmental Services

Philadelphia, PA

Supervisor, Hazardous Material Removal



1997 – 2001 Fairmount Hospital

Roxborough, PA






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