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
Clinical Research Nurse Coordinator, 08/2011 - Current Coastal 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.
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.
Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. As such, it is not owned by us, and it is the user who retains ownership over such content.
How this resume score could be improved?
Many factors go into creating a strong resume. Here are a few tweaks that could improve the score of this resume:
