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Clinical Research Coordinator

Company: Paradigm Clinical Research Centers, Inc.
Location: Redding
Posted on: September 9, 2019

Job Description:

Paradigm Clinical Research Centers is hiring 2 EXPERIENCED Clinical Research Coordinators for the Redding, CA location. ONLY EXPERIENCED CLINICAL RESEARCH COORDINATORS WILL BE CONSIDERED Who we are looking for:An experienced Clinical Research Coordinator who:Is motivated to move the study forward (recruitment and enrollment)Has at least 2 years experience as a Clinical Research Coordinator at a busy Clinical Research facilityIs flexible and works well with othersIs computer savvyIs experienced in knowledgeable in managing regulatory from study start-up though study completion (including knowledge of IRB requirements, forms, and submissions)Is knowledgeable in GCP (GCP certification preferred) Key Skills and Competencies We Are Looking For: CCRC preferred but not required. Must be willing to obtain certification within 1 year of starting employmentExcellent interpersonal, verbal and written communication skillsIn-depth knowledge and experience - perform clinical research duties (including collecting vitals, collecting/processing laboratory samples, ECG), protocols, FDA regulations, and complex visit structures in a clinical research environment.Detail oriented – attention to quality, reliable data, and the ability to manage complex clinical trials.Practical knowledge - Good Clinical Practice (GCP), ICH Guidelines, Human Research Protection --Program (HRPP), IATA Shipping of Blood Specimens, and ability to adapt to and stay abreast of new regulations and technologies related to the conduct of clinical trialsExceptional technical skills - software applications and databases, particularly MS Excel, Word, Outlook and Clinical Research IO eSource platform (a plus) to manage complex and non-routine issues requiring innovative solutions Experience We Are Looking For: At least 2 years of Clinical Research Coordinator experience with knowledge of the design and conduct of clinical trialsIn-depth knowledge of clinical trials, protocols, FDA regulations, and complex visit structuresDirect patient careHands-on experience – reviewing patient records, in conjunction with the PI, for inclusion/exclusion, concomitant medications, and adverse events and knowing how to document the information; working independently to complete projects in a timely manner while prioritizing multiple projects to meet deadlines. What You Will Receive: **Competitive salary, benefits package including medical, paid time off and 401k.Job Type: Full-timeExperience:Clinical: 2 years (Required)Education:High school or equivalent (Required)Location:Redding, CA (Preferred)License:Certificate in Clinical Coordinating (Preferred)Work authorization:United States (Required)Required travel:25% (Preferred)Benefits offered:Paid time offHealth insuranceRetirement benefits or accounts*Site will consider helping with cost of relocation for the right individual*

Keywords: Paradigm Clinical Research Centers, Inc., Redding , Clinical Research Coordinator, Other , Redding, California

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