Clinical Research Medical
Resume:
M. JAY LANGNESS, CCRC
Auburn, KS *6402
(cell): 785-***-****
abj79j@r.postjobfree.com
SUMMARY
** ***** ********** ** ******** research, including coordinating phases I-
IV, administrative, supervisory, business development, recruitment, and
regulatory. 30 overall years in patient care settings.
EXPERIENCE
Truman Medical Center
2301 Holmes St
Kansas City, MO 64108
April 2008-August 2010
Certified Clinical Research Coordinator III
Supervisory position in the Department of Medicine which includes Research
Coordinators in: Pulmonary, Cardiology, Oncology, Internal Medicine, and
Gastroenterology. Also functions as Clinical Research Coordinator "at
large" providing coverage in the absence of the regular Coordinator. Also
tasked with expanding clinical research at the hospital. Recently has
become the GI study coordinator.
Stormont-Vail Hospital, Cotton O'Neil Clinical Research
823 SW Mulane #240
Topeka, KS 66606
785-***-**** ( Mary Martell, Director)
Oct 2006-Dec 2007
Certified Clinical Research Coordinator
Responsible for 5 clinical trials, three diabetes trials, one
hyperlipidemia, and one chronic pain study. Responsible for all aspects of
clinical trials assigned, including regulatory responsibilities,
communication with the host sponsor pharmaceutical companies and
Institutional Review Boards. Investigator meetings, and other duties
relating to clinical research.
Cientifica Inc.
910 E. Douglas Ave.
PO Box 2241
Wichita, KS 67201
Jan 2004-Jul 2006
Clinical Supervisor/Coordinator
Responsible for Cientifica's clinical operations including study
coordination staff, study implementation, staff training, regulatory
compliance and the delivery of quality services to sponsors. Responsible
for study selection, budget negotiation, and physician relations. Integral
member of Cientifica's management team.
University of Kansas Medical Center Research Institute
3901 Rainbow Blvd
Kansas City, KS 66160
Nov 2003-Jan 2004
Temporary Clinical Research Coordinator
Served in a temporary capacity for a special administrative project, and
served at the Research Institute performing administrative research related
activities.
nTouch Research Inc.
4620 J.C. Nichols Parkway, Suite 517
Kansas City, MO 64112
Feb 2002-Feb 2003
Clinical Research Coordinator
Responsible for all inpatient surgical studies at the research center,
specifically orthopedic trials. Maintained positive working relationships
with hospital staff including operating room, nursing staff, pharmacists,
and other ancillary hospital personnel in order to ensure integrity and
accurate execution of the hospital based studies. Also responsible for all
regulatory matters, and interfacing with sponsor pharmaceutical companies.
Supervisory duties included charge of the Research Center in the manager's
absence.
Seattle Clinical Research Center
901 Boren Ave. Suite 1800
Seattle, WA 98104
Jun 1998-Feb 1999
Clinical Research Coordinator
Responsible for all aspects of clinical trials assigned including
Investigators meetings, interpretation and execution of trial protocols and
monitoring of patient adverse experiences. Clinical duties included but not
limited to collection of laboratory samples and interpretation of lab
results in relation to study compounds, ECG and vital signs. Responsible
for meeting with and advising physicians concerning study related matters,
reviewing Informed Consent documents with patients and family members and
working with sponsor pharmaceutical company representatives, FDA and IRB
members. Responsible for all study related administration requirements.
Advanced Research Management
600 Broadway Street
Seattle, WA 98122
Jul 1995-May 1998
Clinical Research Coordinator, Assistant Director of Clinical Research
Duties and responsibilities similar to those listed above. Executed
protocols for Opthalmic Zoster, Peripheral Vascular Disease, Diabetic
Ulcers, NIDDM, HIV, HIV wasting, Heartburn, Smoking Cessation, and
Arthritis. Supervisory duties included Coordinator hire, training, and
supervision. Marketing duties included negotiating with pharmaceutical
sponsors for new studies and contracts. Also represented A.R.M. as the only
non-owner member with full voting rights for a research alliance, a group
of 22 other research sites across the country. This included weekly phone
meetings.
Tulane University School of Medicine
1414 Tulane Ave.
New Orleans, LA 70112
Apr 1992-Jan 1994
Clinical Research Coordinator
Executed clinical protocols in the department. Duties similar to those
previously stated. In addition assisted in the instruction of new Residents
in clinical research.
Clinical Research Center
143 So. Liberty Street
New Orleans, LA 70119
May 1989-Mar 1992
Screening Department Supervisor and Clinical Research Coordinator
Supervised 3 staff members in the screening and recruitment department.
Screened all patients for phase I inpatient trials. After 1990 duties
expanded to include coordination of phase I trials. Phase II and III
studies were done sporadically.
United States Navy
Apr 1978-Apr 1988
Hospital Corpsman and Aviation Medicine Specialist
Served as a Navy Hospital Corpsman for ten years. Obtained broad and
extensive medical, administrative, and supervisory experience. Stationed at
hospitals, a variety of medical clinics, onboard various naval vessels and
in Europe. Functioned as an EMT responding to ambulance requests, and
supervising medical staff members in the field and in the emergency room.
Worked in Internal Medicine, Cardiology, Pediatrics, Emergency Room,
Dermatology, Physical Exams, Medical Records, and Medical Supply. Served as
Aircraft Carrier Flight Deck Corpsman.
EDUCATION AND TRAINING
-USN Hospital Corps School
-Aerospace Medicine School
-EMT-A school
-Medication Dispensing (IV, IM, SC, Oral)
-IV and Phlebotomy
-Suture Certification
-Supervisory and management Training
-Numerous Sponsor Provided Industry Training in Clinical Research, GCP's,
Regulatory and good clinical practices
-ACRP Certification
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