Project Manager Clinical Research
Resume:
Diego Ceniceros, EMT-P,CCRP
San Antonio, TX 78213
************@*****.***
EDUCATION:
Eagle Pass High: Eagle Pass, TX
• Diploma 1991
Texas State Technical: Harlingen, TX
• Cert. of Completion, Emergency Medical Technology 1995-1997
• SoCRA Certification (CCRP) 2009 - current
EXPERIENCE:
Clinical Trials of Texas: 4/2010-4/2012 San Antonio, TX
Clinical Research Coordinator
• Responsible for assisting in conducting research protocols in a manner that ensures quality, consistency, timeliness, accuracy and patient safety
• Performed clinical assessments that included checking vitals, performing phlebotomy, EKG, and completing eCRF’s/CRF’s in a timely manner
• Provided frequent face-to-face, written, and telephone contacts with various persons involved in the study including but not limited to the patients, patient relatives, doctors, pharmaceutical sponsors, pharmacists and all levels of CTT staff
• Responsible for screening potential patients and targets specific study and enrollment goals
Impact Urgent Care: 3/2010-Current San Antonio, TX
Medical Assistant
• Responsible for assisting Physicians and nurses in the diagnostic testing, examination, education, and treatment of patients.
• Perform the following duties under direction of Physicians to assist in examination and treatment of patients:
• Using computer applications
• Answering phones
• Greeting patients
• Updating patient medical records
• Coding and filling superbill
• Interview patients, measure vital signs, height, weight, pulse, respirations, temperatures, ECG’s, establish IV’s and record information in patient charts
• Schedule appointments
• Prepare treatment rooms for examination of patients
• Prepare and drape patients with sterile covering and hand instruments to the Doctor
Phase One Research of Texas: 10/2009-4/2010 San Antonio, TX
Clinical Research Coordinator
• Ensured quality, consistency and accuracy in the conduct of clinical research trials and completion of case report forms
• Performed clinical assessments that included checking vitals, performing phlebotomy, EKG, administering Tuberculin injections and administration of IP
• Responsible for recruiting and screening potential patient candidates as well as performing follow up calls
• Maintained accurate communication with senior project manager, study monitors and related study personnel
Premier Research Group Limited: 5/2006-10/2009 San Marcos, TX
Clinical Research Coordinator I/Clinical Research Coordinator II
• Responsible for conducting and reporting research following protocol administered by the Principal investigator
• Assisted in patient recruitment and eligibility screening for each research project
• Responsible for conducting and compiling individual case reports for each clinical trial
• Performed clinical assessments that included checking vitals, performing phlebotomy, EKG, and administration of IP
Well Med Clinical Research: 7/2003-5/2006 San Antonio, TX
Clinical Research Coordinator I
• Maintained drug accountability, protocol compliance and FDA regulatory compliance maintains updated patient logs on study
• Screened and recruited potential patient candidates for research study including follow up calls to no show candidates
• Responsible for coordinating and constructing research procedures and activities in conjunction with fellow researchers
Healthcare Discoveries: 11/2002-6/2003 San Antonio, TX
Clinical Research Coordinator I
• Responsible for screening potential patients and targets for specific study and enrollment goals
• Coordinated study procedures and activities with participating co-investigators regarding ongoing and/or upcoming studies
• Performed clinical assessments that included checking vitals, performing phlebotomy and EKG’s
SCIREX : 7/2001-11/2002
Clinical Research Coordinator I/Clinical Research Coordinator II
• Responsible for conducting and reporting research following protocol administered by the Principal investigator
• Assisted in patient recruitment and eligibility screening for each research project
• Responsible for conducting and compiling individual case reports for each clinical trial
• Performed clinical assessments that included checking vitals, performing phlebotomy, EKG, and administration of IP
SCIREX: 10/2000-7/2001
Laboratory Coordinator
• Ensured that all shifts related to the laboratory functions were staffed adequately.
• Set daily schedule and informed laboratory staff and CRC staff. Performed laboratory assistant functions as necessary to ensure adequate staffing.
• Ensured maintenance of laboratory records and quality control logs of equipment.
• Oversaw phlebotomy, processing, storage and shipment of lab specimens.
• Trained and documented training in laboratory procedures and ensured that staff met the needs of the research lab.
• Practiced and ensured that laboratory staff practiced GCP and GLP where applicable and followed OSHA regulations and guidelines.
• Reviewed protocols and participated in protocol initiation as requested.
• Ensured that the laboratory and staff were prepared for study start up.
• Worked with all Site Managers and/or Site Office Managers to carry out duties.
THERAPEUTIC AREAS OF EXPERIENCE:
• Osteoarthritis
• Diabetes I & II
• Claudication
• Wisdom Teeth Extraction
• Constipation
• Overactive Bladder
• Cholesterol
• GERD
• Hypercholesterolemia
• COPD
• Bunionectomys Pain Model Study
• Healthy Volunteer Studies
• Hypertension
• Tourettes
• Depression
• Anemia
• Medical Devices
LICENSES/CERTIFICATIONS:
• Emergency Medical Technician-Paramedic, TDH San Antonio, Texas. Re-Certified
• October 2009 Exp: 10/2013
• BLS 7/2010- Current
• ACLS 4/11- Current
• PALS 3/12- Current
• CCPR 2/09- Current
References:
• Frank Rodriguez, Team Supervisor 210-***-****
• Michelle Kelly, Supervisor 210-***-****
• Vanessa Watson, Director of Operations 512-***-****
• Mary Jane Badger, CRA for Roche 801-***-****
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