Clinical Research Nurse Resume Sample 2

Updated on: September 26, 2016

 

You can deem your resume writing efforts successful once an employer deems your resume a success. However, there is no actual way to determine the success of your resume unless of course, you are called in for an interview. Make sure each section of your resume is complete and relevant before you consider sending it out.

Formats matter. So does content. For your reference, here is a sample resume that is both formatted properly and possesses relevant content:

 

Clinical Research Nurse Resume Sample

 

Gayle Lord

488 Shipely Street | Seaford, DE 19958 | (000) 452-7454 | gaylelord @ email . com


 CLINICAL RESEARCH NURSE

Performance Summary: Analytic minded and competent clinical research nurse with extensive experience in designing and implementing clinical research trials. Proficient in coordinating research related activities, educating patients, providing direct patient care and collecting and analyzing patient data and reporting findings according to established protocols. Easy to get along with in addition to possessing a positive outlook to bleak situations.

CORE COMPETENCIES

• Direct Patient Care • Patient Education • Clinical Data Compilation
• Data Assessment • Subject Screening • Procedural Assistance
• Research Processes • Patient Advocacy • Novel Treatment Support
• Charts Management • Review Board Management • Protocol Development

KEY ACHIEVEMENTS
• Awarded for participation in a clinical trial that led to a cure for chronic illnesses
• Singlehandedly created a list of 4800 unlicensed drugs being tested in the country as part of a large research project
• Introduced PIS (patient information sheet) as part of the protocol system, which greatly streamlined patient registration procedures
• Successfully obtained 12 approvals for a clinical study trial, that were in limbo for 2 years

PROFESSIONAL EXPERIENCE

Clinical Research Nurse
Saint Luke’s Health System, Seaford, DE | 6/2011 – Present

• Identify potential clinical study subjects by reviewing existing health information based on inclusion criteria
• Interview potential subjects to determine their suitability for study trials
• Carry out informed consent processes by assisting with registration information and records management
• Ascertain that established clinical study protocols are implemented and maintain protocol integrity
• Monitor participants’ status by ensuring their safety and educate clinical staff on outcomes and expectations

Clinical Research Nurse
City Healthcare, Seaford, DE | 6/2005 – 6/2011

• Performed initial assessments and intake by obtaining social, medical, mental health and substance abuse history
• Educated patients regarding protocol participation
• Provided additional information to ensure participants’ adherence to the program
• Acted as a liaison between primary care and specialty physicians and other clinical provides to refer patients for additional care
• Provided patients with direct care by taking and recording their vitals such as blood pressure, pulse and temperature

Registered Nurse
Mercy Hospital, Seaford, DE| 2/2000 – 5/2005

• Administered medication according to patients’ specific care plans and handled IVs as required
• Educated patients and families regarding their conditions and provided emotional support during distressing times
• Created and maintained patients’ records and charts in a confidential manner
• Obtained blood samples, sent them for testing and followed up on results

EDUCATION
Bachelor of Science in Nursing – 1999
Seaford Nursing School, Seaford, DE