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Data Clinical Research

Location:
San Antonio, TX
Salary:
will discuss
Posted:
December 07, 2011

Contact this candidate

Resume:

Jean A. Davidson, LPN

Clinical Research Coordinator

**** ***** *****

Lenexa, Ks 66219

Phone: 913-***-****

E-mail: st2xt2@r.postjobfree.com

Objective:

To join a clinical research organization as a productive team member and gain career growth while utilizing my in depth clinical research knowledge and experience.

Qualifications:

Tremendous research aptitude with vast knowledge

Good exposure to practical techniques through extensive work experience

Excellent communication and comprehension skills

Quality documentation

Extraordinary ability to maintain quality performance

Adherence to Protocols, GCP/ICH and FDA guidelines

Teamwork

Mentor

Computer skills

Time management

Professional Experience:

Aerotek Staffing Agency/Quintiles, Overland Park, Ks

February 2011- October 2011

Clinical Data Coordinator

Independently and accurately review CRF data for completeness, accuracy and consistency in accordance with all applicable procedures

Accurately and consistently apply data handling conventions to CRF as necessary in accordance with all applicable procedures

Identify and appropriately address data discrepancies in the clinical data via computerized edits and manual checks/listings

Accurately generate data queries to resolve data discrepancies

Appropriately address responses to data queries and accurately update the clinical data as necessary

Vince and Associates Clinical Research, Overland Park, Ks

June 2008 - January 2011

Clinical Research Coordinator

Screening/enrollment of appropriate qualified research subjects Phase I-IV

Accurate completion of source documents and CRF’s/data entry for each subject

Timely completion of data queries

Constant communication with investigators, sponsor company/CRO regarding subjects enrollment and subject visits

Scheduling of all subject visits

Subject recruitment for studies

Ensuring subject safety

Protocol compliance

Performing assessments of subjects, vital signs, EKG, etc

Maintained accurate records of all investigational/non investigational study drug and study supplies

Attend investigator/initiation meetings

Radiant Research, Overland Park, Ks

June 2000 - June 2008

Clinical Research Coordinator/Team Leader

Regulatory document preparation and submission to the Institutional Review Board

Completion of feasibility questionnaires

Screening/enrollment of appropriate qualified research subjects Phase II-IV

Accurate completion of source documents and CRF’s/data entry for each subject

Timely completion of data queries

Constant communication with investigators, sponsor/CRO regarding subject enrollment and subject visits

Scheduling of all subject visits

Subject recruitment for studies

Ensuring subject safety

Protocol compliance

Performing assessments of subjects, vital signs, EKG, PFT’s, phlebotomy, etc

Maintained accurate records of all investigational/non investigational study drug and study supplies

Scheduling monitoring visits

Attend investigator/initiation meetings

Quintiles, Overland Park, Ks

1998 - June 2000

Clinical Data Coordinator

Performed quality control checks for clinical data management documents

Completed case report forms to perform verification and database connections to clinical databases

Issuing queries

Update study database based on query resolution

IMTCI, Lenexa, Ks

1990 - 1998

Clinical Research Coordinator/Team Leader

Screening/enrollment of appropriate qualified research subjects Phase I-IV

Accurate completion of source documents and CRF’s/data entry for each subject

Timely completion of data queries

Constant communication with investigators, sponsor/CRO regarding subject enrollment and subject visits

Scheduling of all subject visits

Subject recruitment for studies

Ensuring subject safety

Protocol compliance

Performing assessments of subjects, vital signs, EKG’s, PFT’s, phlebotomy, etc

Maintained accurate records of all investigational/non investigational study drug and study supplies

Scheduling monitoring visits

Attend investigator/initiation meetings

Providence - St. Margaret Health Center, Kansas City, Ks

1980 - 1990

Licensed Practical Nurse/Floor Nurse

Managed priorities in a fast paced environment geared toward safe and competent patient care

Administrative experience of admission/assessment treatments, evaluation and education for a wide range of patients

Provided patient and family teaching

Followed physicians orders

Documented nursing reports

Education:

Area Vocational Technical School, Kansas City, Ks

Licensed Practical Nurse, 1980

Volunteer Experience:

Salvation Army bell ringer

Welcome Hero’s home

Aid with military families

Assist and educate ill patients and their families

License and Certificate

Licensed Practical Nurse, State of Ks

American Heart Association - CPR & AED

Nursing Continuing Education Units

Good Clinical Practice (GCP) Accreditation, 2011

References upon request



Contact this candidate