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Clinical Research Coordinator

In New Jersey / United States

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Clinical Research Coordinator   

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JOB TITLE:
Clinical Research Coordinator
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Franklin Lakes New Jersey / United States

JOB DESCRIPTION :

Job Description:

  • Serve as the primary contact to ensure appropriate communications, trial management, and meeting of timelines.
  • Coordinating the operational aspects of new and ongoing clinical trial at the site.
  • Work under the supervision of the Principle Investigator(s), while exercising excellent clinical judgment in patient monitoring and care.
  • Maintain daily contact with the Principle Investigator(s) for recruitment activities, study start up, and general daily communication.
  • Responsible for the execution of the protocol and ensuring that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained on the protocol.
  • Patient recruitment and pre-screening.
  • Maintain and submit IRB communications and regulatory documents.
  • Timely communication with internal teams, investigators, review boards, and study subjects.
  • Prepare other study materials as requested by the Principal Investigator such as informed consent documents, case report forms, enrollment logs and drug/device accountability logs.
  • Willingness for some travel is a requirement for this position.
  • Other duties as assigned.

Qualifications:

  • At least Three years of experience as a CRC is required.
  • Ability to check and document vitals as well as EKG (ECG).
  • Phlebotomy experience is a plus.
  • Good management and organizational skills, understanding of medical procedures, exceptional interpersonal skills, the ability to work independently

Position Details

S16174661686503732
New Jersey / United States
Franklin Lakes
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Clinical Research Coordinator    Apply

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Job Description:

  • Serve as the primary contact to ensure appropriate communications, trial management, and meeting of timelines.
  • Coordinating the operational aspects of new and ongoing clinical trial at the site.
  • Work under the supervision of the Principle Investigator(s), while exercising excellent clinical judgment in patient monitoring and care.
  • Maintain daily contact with the Principle Investigator(s) for recruitment activities, study start up, and general daily communication.
  • Responsible for the execution of the protocol and ensuring that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained on the protocol.
  • Patient recruitment and pre-screening.
  • Maintain and submit IRB communications and regulatory documents.
  • Timely communication with internal teams, investigators, review boards, and study subjects.
  • Prepare other study materials as requested by the Principal Investigator such as informed consent documents, case report forms, enrollment logs and drug/device accountability logs.
  • Willingness for some travel is a requirement for this position.
  • Other duties as assigned.

Qualifications:

  • At least Three years of experience as a CRC is required.
  • Ability to check and document vitals as well as EKG (ECG).
  • Phlebotomy experience is a plus.
  • Good management and organizational skills, understanding of medical procedures, exceptional interpersonal skills, the ability to work independently