Clinical Research Coordinator
Clinical Research Advantage - Colorado

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At Clinical Research Advantage, Inc. we understand that our greatest asset is the skills and talents of our people and they are truly what set us apart!

Clinical Research Advantage is a leader in outsourced trial management services to the pharmaceutical, biotechnology and medical device industries. CRA has completed over 1,800 clinical trials in its 20 years. CRA is comprised of community based Investigators plus an experienced staff of Clinical Research Coordinators. CRA currently operates from its 33 site network across seven states. The key to our success has been the development of research departments within established medical practices. Our research staff is positioned in the clinic, which affords CRA rapid recruitment of reliable, qualified subjects into clinical trials. Our expertise continues throughout the trial, providing full execution of the protocol with complete and accurate data. CRA enjoys a strong reputation for quality and is focused on patient care.

We are currently looking for a Clinical Research Coordinator for our Denver, Colorado site location. The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to CRA’s SOPs, GCP and FDA/ICH guidelines. Ensures IRB approved protocols are implemented and followed. Executes informed consent process and monitors patient status and safety; collects and organizes research data; schedules and conducts study specific training and site in-services to study related staff on new or amended protocols; educates patients and their families about treatments and possible side effects. The Clinical Research Coordinator must also be able to perform clinical tasks (i.e. phlebotomy, EKGs, vital signs, etc.). CRCs typically perform tasks such as:

Site preparation

Obtaining informed consent

Patient screening and recruitment

Patient enrollment

Conducting study visits

Maintaining and dispensing study product and supplies

Completing and ensuring the quality of case report forms

Maintaining source documents

Ensuring site quality

Responding to queries in a timely manner.

Required Qualifications :
A Bachelor’s degree and a minimum of 2 years of experience as a Clinical Research Coordinator, or an equivalent combination of education and experience, is required. An RN credential is a plus. Certification as a Clinical Research Coordinator is preferred;

Proficiency with clinical duties such as vitals, phlebotomy, etc.;

Strong proficiency with Microsoft Office programs (Outlook, Word) and Web applications;

Exceptional organizational skills, attention to detail and follow through;

Ability to type proficiently (35+ wpm);

Well developed verbal and written communication skills;

Well-developed interpersonal skills and the ability to work well independently as well as with coworkers, peers, supervisors, management and external customers;

Ability to effectively and efficiently handle multiple priorities and tasks simultaneously with precision and adapt to changes in responsibilities and workloads;

Must be professional, possess a high degree of urgency and self-motivation and have a strong work ethic;

Must possess a high degree of integrity and ability to maintain confidentiality with HIPAA guidelines, patient matters and other confidential information.

Join Clinical Research Advantage as we expand and become an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do!

You'll enjoy competitive compensation and an exceptional benefits package that includes: Medical, Dental and Vision Insurance, Life and AD&D Insurance, disability, 401K Plan, a competitive program of time off and more.

To learn more about our company visit us as

Clinical Research Advantage - 4 months ago - save job - block
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