Yyyyyy x. yyyyyy

Experienced Registered Nurse with several years of experience in high-volume environments along with a strong background in administrative roles within a healthcare setting. Experienced in assisting with drug trial administration, obtaining patient medical histories, reviewing medical records, overseeing nursing staff scheduling, and facilitating quality improvement initiatives. Equipped with a significant level of communication and interpersonal abilities in addition to a strong background in effectively fostering positive relationships with others.

Healthcare Administrative Support Drug Trial Management Coaching/Training Patient Education

Staff Schedule Management Database Management Creating Source Document

Trial Validity & Consistency Regulatory Standards Compliance Process Improvement

  Direct day to day clinical safety logistics within a fast-paced environment with a focus on increasing productivity and efficiency levels

  Play a lead role in the assessment, monitoring, follow-up, and reporting of large-scale drug trials in addition to generating reports on potential adverse actions

  Maintain an expert level knowledge of regulatory safety requirements and update information using various database tools (RAVE, Inform, Oracle, AWARE, AEGIS)

  Instrumental in evaluating individual cases for validity and consistency, review source documents, and successfully prioritize cases based on importance

  Oversaw nursing and administrative functions within a busy medical center which included working closely with patients of all ages within a variety of units

  Held several roles which included Endoscopy Nurse, Chemotherapy and Biologic Therapy Nurse, and Research Nurse Coordinator-Oncology

  Worked closely with both sponsors and CRO s in the design of IRB submissions, revisions, and consent materials in addition to leading recruitment efforts for study participants

  Scheduled both initial and follow-up patient visits, documented reported data in regard to research progress, identified adverse reactions, and updated results information

  Maintained an expert level knowledge of regulatory requirements, developed source documents, and generated comprehensive study reports

Additional Professional Experience Includes: Staff Nurse, Saint Barnabas Medical Center (1990-2001)

Yyyyyy x. yyyyyy

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Dear__________________:

I am currently seeking a challenging new career opportunity as (JOB TITLE) and am submitting my resume for your review. In advance, thank you for your time and consideration.

As demonstrated in the accompanying resume, my professional qualifications include a strong background in nursing and administrative roles with experience in managing administrative functions related to drug trials, monitoring patients for adverse reactions, and managing information using various database tools. In addition, I have strong experience in reviewing source documentation and ensuring regulatory standards are met.

To complement my professional experience, I also possess stellar interpersonal and communication skills with an impressive educational background which includes a Bachelor of Science in Nursing from the University of Phoenix (Expected 2018).

As an employee, you will find me to be a driven team player committed to supporting you in achieving your objectives through superior performance. I am confident that I could be a valuable asset to your organization, and look forward to interviewing with you in the near future.

Sincerely,

Yyyyyy x. yyyyyy