Julieann Murray
* ********** **, **********, ** *7439
201-***-**** – ace13r@r.postjobfree.com
Professional Overview
My position as a Clinical Safety Analyst has left me with a strong desire to focus on a career in the Clinical
Sciences. To enhance my career move, I am also a recent graduate, who on academic scholarship was able to
attain my goal of a Bachelors in Biology.
Most of my career has been spent as a Licensed Practical Nurse with over 15years of experience in patient care,
case management, coordination of services, and staff supervision. Leading to my strong medical knowledge
base.
•
Core Qualifications Skilled medical nurse from pediatrics to
geriatrics.
• Knowledge of Good Clinical Practice ICH
guidelines.
• Case management of hospice, and diabetic
• programs.
Knowledge of Clinical Safety Data
Management ICH-E2A.
• Certified in Phlebotomy
• Clinical Safety investigation experience in
• Lymphedema Pump Therapy certified.
Serious Adverse Events or Adverse Drug
Reaction reporting, collection, and follow-
• Insulin Pump Therapy certified.
up investigation.
•
Accomplishments
• Medical proficiency and ability to apply knowledge to a variety of positions held.
• Collaborated with patients, physicians to plan and implement patient care, and family support.
• Maintained compliance within GCP, and ICH guidelines for position in Drug Safety.
• Knowledge of reporting time frames for ADRs.
• Experienced in narrative writing.
Education
Bachelor of Science : Biology, 2014
East Stroudsburg University of Pennsylvania – East Stroudsburg, PA, Monroe.
Attended on an academic scholarship.
Associate of Arts : Psychology, 2012
Sussex County College – Newton, NJ, Sussex.
Graduated with honors. Phi Theta Kappa
Practical Nurse : Practical Nursing 1984
Erie Boces I – Lancaster, NY, Erie.
Held licensure in NY & NJ.
Experience
Volunteer Laboratory Technician
May 2014 to June 2014
ESU Northeast Wildlife DNA Laboratory - East Stroudsburg, NJ
Volunteer specializing in tic identification. Lyme, Babesia, Tularemia testing was performed via DNA,
PCR, and Gel Electrophoresis.
Clinical Safety Analyst (Contactor through Manpower)
February 2007 to February 2009
Abbott Laboratories Immunology Division– Parsippany, NJ
• Coordinated the safety activities for phase III global clinical trials within the Immunology therapeutic
area, including indications for Ankylosing spondylitis, Crohn’s disease, Rheumatoid arthritis, and
Psoriasis.
• Expedited reporting of Serious Adverse Events (SAEs) from the investigator site, CRO and/or affiliates
which were also submitted to pharmacovigilance department in accordance with ICH guidelines on
Clinical Safety Data.
• Contacted the SAE reporting party to solicit follow-up information until the event is satisfactorily
resolved.
• Researched, followed up and resolved SAE queries in coordination with the study data management
teams.
• Performed medical review of protocol, safety-specific data, as defined by a protocol-specific safety
review plan, in accordance with GCP and ICH guidelines.
• Responsible for updating protocol-specific drug safety plans.
• Lead SAE/pre-termination narrative writer, as required for Clinical Study Report submission.
• Effectively communicated with the study-designated physicians (SDP), clinical teams, CROs, affiliates,
European counterparts, investigator sites, and other departments as necessary.
High Tech Home Care Practical Nurse
July 2001 to September 2006
Loving Care Pediatric Home Care – Fort Lee, NJ
• I was responsible for pediatric patients needing high tech medical care.
• Infants and children cared for included patients that were ventilator dependent, having need for nasal, or
gastric tube feedings, catheterizations, wound care, tracheostomy care, injections and phlebotomy.
• Skills needed for such care included proficiency with tracheostomy and gastrostomy care/maintenance.
• Knowledge of various durable medical equipment needed to complete individualized patient care needs.
Clinical Coordinator
January 1999 to June 2001
Comprehensive Home Care – South Orange, NJ
• Competitive scheduling of services between nurses and patients for home infusion companies.
Case Manager/Clinical Coordinator/In-service Trainer
May 1997 to May 1999
Coram Resource Network – Whippany NJ
• Responsible for the entire hospice case management contract under Aetna US Healthcare.
Single contact case manager for the diabetic program under the Aetna US Healthcare contract.
Instructor for our in-service training of new hires on case management, hospice and Medicare
guidelines.
Licensed Practical Nurse
February 1993 to M ay 1997
Randolph Medical and Renal Associates - R andolph, NJ
• Responsibilities included coordination of doctors and patients office visits.
• Medical tasks included patient vital signs, ECGs, x-ray development, injections, and patient calls.
• Also responsible for documentation of patient visits, and all procedures performed during office
visits.
• One of two nurses responsible for three physicians and 18,000 patients.
Clinical Coordinator
January 1990 to March 1993
Caremark Incorporated, CSS - Parsippany, NJ
• My division was the exclusive contracted provider, for the closed packaging system of the drug
Clozaril for Sandoz Pharmaceuticals. Sandoz received approval from the FDA for the
introduction of Clozaril, under a bundled system of enforced blood work for white blood counts
to insure prior to release of drug to subject that they were not leucopenic.,
• My further responsibilities included client scheduling for strict blood monitoring regimen, drug
distribution, client and public relations, and charting.
References upon request.