Dedicated [Job Title] with experience coordinating and carrying out clinical research studies. Talented at screening patients, administering medication, collecting samples for laboratory testing and clinical investigation recordkeeping. Familiar with regulatory aspects, FDA submission process and IRB requirements. Dedicated Clinical Research Coordinator experienced in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer [Number] years' experience in the field and take on a fast-paced position.
Skills
Research Experience
Documentation Requirements
Trial Oversight
Training & Development
Organizational Skills
Working Collaboratively
First Aid/CPR
Critical Thinking
Team Building
Problem Resolution
Work Ethic
Experience
08/2011 to Current
Clinical Research Nurse CoordinatorCoastal Pediatric Associates – Summerville, SC,
Screened research study candidates for eligibility and obtained consent documentation.
Documented case report forms and collected data for study research logs.
Relayed information such as requirements and instructions from clinical team to study participants.
Recruited, interviewed and enrolled patients to increase number of participants.
Prepared for upcoming studies by collaborating with program leaders to determine facility and staff needs.
Obtained informed consent from research subjects and guardians to explain possible side-effects and potential outcomes of [Type] research.
Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.
Conducted informed consent presentations and maintained documentation.
Assessed records of each patient, reviewed databases and checked referrals to locate potential research study participants.
Kept patient care protocols and clinical trial operations in compliance.
Collected, processed and delivered specimens from trial participants.
Managed clinical research trials involving [Type], [Type] and [Type] disorders.
Coordinated protocols by organizing and prioritizing all activities associated with [Type] studies, including [Type], [Type] and [Type].
Spearheaded [Type] trials from initial visits and meetings through completion in accordance with schedule and budget demands.
Worked closely with team members to deliver project requirements, develop solutions and meet deadlines.
Collected vital signs and laboratory specimens to facilitate testing.
Observed patients after administration of designated medication for adverse events.
Worked successfully with diverse group of coworkers to accomplish goals and address issues related to our products and services.
12/2001 to 08/2011
Ambulatory Oncology Registered NurseCleveland Clinic – City, STATE,
Provided patients with information on range of subjects, not limited to side effects from chemotherapy and benefits of proper nutrition during treatment.
Expertly explained diagnoses to patients and discussed next steps for treatment and care in easy-to-understand terminology.
Wrote detailed notes regarding patient discussions in patient charts.
Observed strict safety measures, including checking medication dosages before administration to patients.
Helped patients and families feel comfortable during challenging and stressful situations, promoting recovery and reducing compliance issues.
Delivered information regarding care and medications to patients and caregivers in comprehendible terminology.
Executed appropriate steps for patient treatment following careful review of physician medical regimen.
11/1994 to 12/2001
Oncology Staff Registered NurseCleveland Clinic – City, STATE,
Administered chemotherapy to patients as indicated by chart instructions given by each physician.
Emotionally supported patients receiving treatment by carefully listening and offering comfort.
Wrote detailed notes regarding patient discussions in patient charts.
Assessed patient conditions, monitored behaviors and updated supervising physicians with observations and concerns.
Advocated for patient needs with interdisciplinary team and implemented outlined treatment plans.
Observed strict safety measures, including checking medication dosages before administration to patients.
05/1993 to 11/1994
Oncology Staff Registered NurseCleveland Clinic – City, STATE,
Administered chemotherapy to patients as indicated by chart instructions given by each physician.
Wrote detailed notes regarding patient discussions in patient charts.
Assessed patient conditions, monitored behaviors and updated supervising physicians with observations and concerns.
Advocated for patient needs with interdisciplinary team and implemented outlined treatment plans.
Education and Training
Expected in 05/1993 to to
Associate of Applied Science: Nursing Lakeland Community College - Willoughby, OH GPA:
Expected in to to
Bachelor of Science: RN-BSN Indiana Wesleyan University - Marion, IN GPA:
Activities and Honors
Oncology Certified Nurse
Oncology Nursing Society member
Collaborative Institutional Training Initiative training in human subjects research protection
Sigma Theta Tau International Honor Society of Nursing
Certifications
Licensed Registered Nurse - 1993 to present
Oncology Certified Nurse License - 1997 to present
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