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Clinical Research Coordinator - Bellevue, NE

Asthma & Allergy Center Bellevue, NE
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Job Description

Clinical Research Coordinator - Bellevue, NE

We are looking for a highly motivated, responsible individual to coordinate clinical research trials dealing mainly with asthma and allergic disease. Must be detail-oriented, well organized with excellent planning and language skills, both oral and verbal, and able to work independently. Responsibilities include screening patients, testing and evaluating patients, documentation, and working with pharmaceutical and regulatory agencies. The candidate should possess knowledge and insight into legal and regulatory matters concerning clinical research. Requires a background in an allied health field, an interest in research, and computer skills.

We are a non-smoking facility.

www.asthmaandallergycenter.com

 Personal Traits

  • Strict attention to detail
  • Highly developed organizational skills
  • Ability to work with multiple study protocols
  • Excellent verbal and written communication skills
  • Interpersonal and problem-solving skills
  • Self-motivated, results oriented, able to work independently 
  • Ability to work a flexible schedule with some travel
  • Communicate effectively and tactfully with others within the clinic and especially with the public
  • Ability to organize workload to determine priority of duties

 

  • Qualifications:
  • Background in an allied health field is required although a nursing degree is preferred
  • A minimum of one year of experience as a study coordinator preferred; certification in research (ACRP) preferred.
  • Computer literacy in word processing, spreadsheet and database applications
  • Knowledge of FDA regulations and GCP guidelines preferred
  • International Air Transport Association (IATA) certification is a plus (will train)
  • BLS or must complete within six months of hire

    Tasks  

  • Clinical trial preparation for pharmaceutical protocols
  • Development and evaluation of patient information and informed consent forms and patient recruitment
  • Recruitment and coordination of the patient with regard to informed consent, screening and inclusion of the subjects adhering to safety and compliance issues
  • Coordination and management of the clinical trial, communication with sponsor, visit coordination, sampling, time management and product accountability
  • Data collection and management, collection of source documents, using and developing CRFs, registration and management of AEs, filing and archiving, managing monitoring visits, dealing with queries
  • Close-out of the clinical trial, audit preparation, and trial closure
  • Attendance at Investigator Meetings

Job Details

Date Posted August 23, 2019
Date Closes September 22, 2019
Located In Bellevue, NE
Job Type Full-time Employee
Compensation Hourly Wage, Varies, Based on Experience
Shift Custom
Mon: 8 am to 4 pm
Tue: 8 am to 4 pm
Wed: 8 am to 4 pm
Thu: 8 am to 4 pm
Fri: 8 am to 4 pm
Hours 40 hours per week; Great Pay and Benefits!
SOC Category 11-9121.01 Clinical Research Coordinators
Zipcode 68123
Name Hiring Manager
Address 3503 Samson Way, Suite 108
City, State and Zip Bellevue, NE 68123

This job requires the following skills

  • STRUCTURE (C/F Data Systems)
  • Computer Usage
  • Excellent Communications
  • Strong Flexibility / Adaptability
  • Strong Time Management
  • Strong Work Ethic
  • Nursing Clinical Development
  • Medical Education / Training
  • E-ClinicalWorks
  • Allergy, Asthma and Immunology
  • Clinical Research
  • Phlebotomy Technician
Location