cardiovascular research clinical coordinator resume example with 20+ years of experience
JessicaClaire
Montgomery Street, San Francisco, CA94105609 Johnson Ave., 49204, Tulsa, OK Home: (555) 432-1000 - Cell: - resumesample@example.com - : - -
Professional Summary
Patient-centric Clinical Researcher with over 15 years' combined experience as a Clinical Research
Coordinator and Registered Nurse. Excellent communicator that exhibits superior interpersonal,
organizational, and negotiation skills. Dedicated medical professional armed with remarkable scientific
and technical expertise. Determined to make life better for people around the world.
CORE QUALIFICATIONS
Clinical Research & Planning Regulatory Support
Clinical Trial Coordination Confidential Information Management
Trial Execution & Support Cross Functional Team Collaboration
Scientific Data Dissemination Business & Customer Support
Skills
quick learner
dependable hard worker
Work History
2016 to 2017
Cardiovascular Research Clinical CoordinatorFairview Health Services – Brooklyn Park, MN,
03/2008 to 03/2015
Anticoagulation NurseCvph Medical Center – Plattsburgh, NY,
Monitored all anti-coagulation patients per protocols.
Developed, coordinated, and delivered patient and staff education.
Covance; Indianapolis / Evansville, Indiana 2000 - 2008
Global Project Manager - Central Lab Services (2008).
Participated in training for supply chain management of lab kits for all clinical trials.
2007 to Current
Clinical Operations SupervisorBaylor Scott & White Health – Prosper, TX,
Led and directed clinical operations at a top performing site for phase one studies.
Managed 90-bed inpatient phase one clinic and oversaw a feasibility study and bid process for
budgeting of a trial.
Supervised staffing and training of approximately 60 Registered Nurses and Medical Assistants
and decreased agency staffing by 60 - 70%.
Cross trained all medical and non-medical staff to perform study tasks.
Monitored performance of Clinical Research Organization to ensure compliance with study
protocols, SOPs, and ICH/GCP regulations and study specific manuals and procedures.
Assessed need for, ordered, obtained and interpreted appropriate lab tests.
Conducted mandated health screenings, physicals and special education assessments in [number] schools with [number] students. Ensured external follow-up where required.
Chronic patient care in med-surg unit, adeptly handling all aspects of treatment from medication to wound care to monitoring for [number] patients per shift.
Chronic patient care in med-surg unit, adeptly handling all aspects of treatment from medication to wound care to monitoring for [number] patients per shift.
2000 to 2006
Clinical Research CoordinatorUniversity Of Tennessee Medical Center – Knoxville, TN,
Recognized for outstanding study performance by a small pharma organization.
Developed and implemented study team logistics for all in-house phase one trials.
Prepared and submitted documents to Institutional Review Board and coordinated and
conducted phase one clinical trials.
Initiated protocol review, participated in study planning, conducted subject enrollment and
visits, documented adverse events, and maintained source documents.
Prepared for study visits with monitor, sponsor, or auditor.
Assisted with updating and implementation of SOPs in union with the regulatory department.
1990 to Current
Staff NurseDepartment Of The Air Force – , ,
Coordinated and implemented initiatives relative to wellness promotion.
Assisted in making decisions regarding health and medical services and treatments.
Documented assessments, diagnosis, interventions, and outcomes.
1991 to 1997
Jessica Claire, RNInternists Of Southern Indiana – City, STATE,
1990 to Current
Office Staff NurseBristol Hospital – City, ,
1988 to 1990
Cardiac Care NurseKettering Medical Center – City, STATE,
Current to Current
Critical Care NurseMiami Valley Hospital – City, STATE,
Demonstrated advanced skills to care for critically ill patients who are at high risk for life
threatening problems and illnesses.
Assessed, planned, and implemented patient care.
Collaborated with fellow members of critical care team.
Acted as an expert in evaluating intensive care patients, administered care, recognized
complications, and coordinated with team members.
Provided advanced life support, assisted physicians with procedures, and monitored ventilators
and other life support equipment.
Administered IV medications and utilized nursing standards and protocols for treatment.
Acted as an integral code team member and participated in preceptorship and mentoring.
Interests
Holy Rosary School; Evansville, Indiana 1998- 2002
School Nurse
· Maintained student immunization and health records and conducted state require student
screenings, acting as a volunteer.
Education
Expected in 2009 to to
Anticoagulation Therapy Management Program: University of Southern Indiana - Evansville, Indiana GPA:
Expected in 2007 to to
Certified Clinical Research Coordinator (CCRC): American Clinical Research Academy - Louisville, Kentucky GPA:
Expected in 2006 to to
Advanced Cardiac Life Support (ACLS): American Heart Association - Evansville, Indiana GPA:
Expected in 1991 to to
Pulmonary Function Certification: University of Cincinnati - Cincinnati, Ohio GPA:
Emphasis in [Name of Emphasis]
Emphasis in [Name of Emphasis]
Expected in 1987 to to
Bachelor of Science: Nursing University of Evansville - Evansville, IN GPA: Nursing
Expected in 2007 to to
Six Sigma;: University of Evansville - Evansville, Indiana GPA:
LICENSE & CERTIFICATIONS
Registered Nurse: License Number 28111690A
VOLUNTEER EXPERIENCE
Holy Rosary School; Evansville, Indiana 1998- 2002
School Nurse
· Maintained student immunization and health records and conducted state require student
screenings, acting as a volunteer.
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