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Clinical Research Coordinator

3 months ago

Idaho Falls, United States Rocky Mountain Clinical Research Full time
Job DescriptionJob Description

Rocky Mountain Clinical Research of Idaho Falls, ID is looking to hire a full-time Clinical Research Coordinator. Are you interested in advancing your medical or nursing career? Do you want to work for a healthcare organization where your work has a positive impact on the lives of its patients? If so, please read on

This clinical-research position earns a competitive wage of $17 - $25 per hour depending on education, training, and experience. We also offer great benefits, including medical, dental, vision, a 401(k) plan, and paid time off (PTO). If this sounds like the right clinical research opportunity for you, apply today


ABOUT ROCKY MOUNTAIN CLINICAL RESEARCH

Our research organization was founded on the principle of advancing medical care for patients who struggle with disease. We provide in-depth clinical research for all types of illnesses, including diabetes. From medications to medical devices, we are on the cutting edge of clinical research. Our studies determine the safety and effectiveness of a new product compared to a gold standard or similar treatment. Through our clinical study involvement, we help bring new treatments to the market for many diseases and make it easier for all patients to manage their health while ensuring their safety. We strive to provide a refuge from the storms of life where those who are ill can come to be refreshed and replenished.

We are a family-oriented company that values our employees. If you are an outdoor enthusiast, you'll love that we are located close to the beautiful Rocky Mountains. Our team enjoys great benefits and the opportunity to work on the leading edge of medical technology.


A DAY IN THE LIFE OF A CLINICAL RESEARCH COORDINATOR

As a Clinical Research Coordinator, you play a key role in the day-to-day operation of ongoing studies. Working with the research director, principal investigator, and the coordinators, you coordinate and administer clinical trials under the direction of the Principal Investigator. You formulate, implement, and organize processes to ensure the successful operation of each trial. With a high level of accuracy and attention to detail, you complete all follow-up paperwork and documentation.

While you love working with patients, you will also enjoy the administrative aspect of your job. Your medical or nursing background helps you to connect with subjects participating in studies, while ensuring their safety. To run our studies according to established protocols, you become an expert on good clinical practices. You also work hard to ensure that each clinical study is performed in accordance with federal and international regulations. You take pride in the work you do to maintain and coordinate all of our studies


QUALIFICATIONS

  • Medical background
  • Strong clerical skills
  • Excellent interpersonal skills

Certified medical assistant (CMA), licensed practical nurse (LPN), or higher credentialing is preferred but not required. Experience in a healthcare or research environment would be a plus. Do you have good analytical and decision-making skills? Are you detail-oriented? Can you maintain a good bedside manner with patients? Are you passionate about quality control? If so, you might just be perfect for this position


WORK SCHEDULE

This full-time clinical study position typically works Monday - Friday.


READY TO JOIN OUR TEAM?

We understand your time is valuable, so we have a very quick and easy application process. If you feel that you have the right medical or nursing background for this clinical study job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you

Location: 83404