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Clinical Research Coordinator

Requisition Number 4615953344 Date posted 10/08/2020 Location Browns Mills, New Jersey

Job Details

Description

Position Summary:Within the department of Clinical Research, and under the funding provided by Sponsor Organizations, the Clinical Research Coordinators performs their duties under the guidance Senior Research Specialist and in accordance with DHLC Clinical Research Standard Operating Procedures. Performs data abstraction, collection, and entry to support clinical research. Prepares IRB communications. Submits reportable events. Ensures compliance with prescribed interventions and evaluations of the assigned protocol(s). Provides data to the collaborating research organization or study sponsor. Prepares data reports. Works closely with Clinical Research staff, Principal and Co-Investigators to help set up and coordinate trials, keep track of developments while clinical trials are going on, and complete the clinical trials.

Experience

  • Required: 1-2 years of medical-related clinical and/or research experience
  • Preferred:Cardiovascular experience preferred.
  • Education

  • Required: N/A
  • Preferred: Associates degree or above in a healthcare or science-related field preferred Applicable certification or commensurate cardiovascular or military experience will be considered in lieu of degree.
  • License and Credentials

  • Required: N/A
  • Preferred:Candidate will be encouraged to become certified as a Clinical Research Coordinator after 2 years of full time research-related work if not already certified. Certificate of successfully completing Good Clinical Practice (CITI training or comparable training) within one month of hire.
  • Skills

  • Required: Must be able to meet deadlines and prioritize workload and complete multi-step procedures on several studies simultaneously. Knowledge and experience with medical and scientific terminology and concepts. Effective communication and interpersonal skills. Demonstrated ability to prioritize and multitask to meet multiple deadlines. Fluency in English (oral or written.) Proficiency in MS Outlook, Word, Excel. Working knowledge of general scientific research. Ability to work independently and as part of a team.
  • Preferred:N/A
  • Bi-Weekly Hours: 80

    Work Schedule: M - F

    Qualifications

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