IRMA G ATHEY

***** ******** ****, *** *******, Texas 78233

Home: 210-***-**** - Cell: 210-***-****

hsgl33@r.postjobfree.com

Clinical Research Coordinator with 9 years experience and Licensed Vocational Nurse. Able to function well in fast paced environment and multiple tasks. Reliable and ability to work well independently and in a team setting. Strong relationship-building skills with patients and coworkers.

• Bilingual (Spanish)

• GCP Certificate (current)

• IATA Certified (current)

• CPR Certified (current)

• Intravenous Therapy Certified

• Phlebotomy

• Patient Recruiting

• Numerous EDC Training (Inform, Rave, Macro, ePro,Oracle)

• Computer Literate

• Phase I, II, III, IV studies

• Numerous Study required procedures

RESEARCH EXPERIENCE:

Clinical Research Coordinator

October 2007 to March 2012

Texas Arthritis Research Center – San Antonio, Texas

• Evaluates, plans, implements and documents scientific research utilizing human

subjects (attends investigator meetings, prepares regulatory documents, prepares source

documents, interacts with sponsor, works under supervision of PI and participates in monitor

visits).

• Identifies and interviews potential subjects (identification made from referrals or advertising;

potential subjects interviewed for inclusion per protocol I/E criteria)

• Gathers sample data from human subjects following specific protocols (vital signs, protocol

specific procedures such as lab collection with submission-EKGs-completion of

diaries/questionnaires dispensation/collection of study IP, collection of AEs, subject

follow-up, CRF completion).

Clinical Research Coordinator

August 2006 to February 2007

Road Runner Research – San Antonio, Texas

• Evaluates, plans, implements and documents scientific research utilizing human

subjects (attends investigator meetings, prepares regulatory documents, prepares source

documents, interacts with sponsor, works under supervision of PI and participates in monitor

visits).

• Identifies and interviews potential subjects (identification made from referrals or advertising;

potential subjects interviewed for inclusion per protocol I/E criteria)

• Gathers sample data from human subjects following specific protocols (vital signs, protocol

specific procedures such as lab collection with submission-EKGs-completion of

diaries/questionnaires dispensation/collection of study IP, collection of AEs, subject

follow-up, CRF completion)

Clinical Research Coordinator

February 2003 to July 2006

Innovative Clinical Trials – San Antonio, Texas

• Evaluates, plans, implements and documents scientific research utilizing human

subjects (attends investigator meetings, prepares regulatory documents, prepares source

documents, interacts with sponsor, works under supervision of PI and participates in monitor

visits).

• Identifies and interviews potential subjects (identification made from referrals or advertising;

potential subjects interviewed for inclusion per protocol I/E criteria)

• Gathers sample data from human subjects following specific protocols (vital signs, protocol

specific procedures such as lab collection with submission-EKGs-completion of

diaries/questionnaires dispensation/collection of study IP, collection of AEs, subject

follow-up, CRF completion).

OB Gyn Office Nurse, Team Leader

December 1998 to December 2002

Institute for Women's Health – San Antonio, Texas

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