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Clinical Research Coordinator - Syracuse, NY

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The Clinical Research Coordinator is responsible for the operational aspects of clinical trials and ensures studies are conducted according to the GCP/ICH guidelines, other federal and state regulations.  They assist the Principal Investigator with all research activities ranging from determining project feasibility to study closure.

  • Work with outside sources to locate new study opportunities and distribute to proper Investigators interested in doing Research
  • Collaborates with Investigator on new Clinical Studies and completes the Initial Submission to the Investigator Review Board (IRB)
  • Coordinates and attends all Pre-Study/Study Site visits with Sponsor and Investigator
  • Manages the updates of all study regulatory documents such as: Amendments, Continuing Reviews, AE/SAE tracking/reporting, Human Studies Tracking log, training requirements, medical licenses, Curriculum vitae
  • Meet with Study Monitors when necessary per protocol
  • Submission and maintenance of sponsor IND safety reports to IRB
  • Participant screening and randomization as per protocol
  • Scheduling patient visits
  • Explain consent and HIPAA process and assist patient in completion of forms before any other study related activity is performed
  • Collection, processing and shipping of protocol related laboratory specimens

 

Salary is $42K+ DOE and strong benefits package.  Direct placement opportunity.

 

Education:  Associates Degree

Experience:  4 years experience coordinating clinical research projects

  • Ability to communicate effectively both in person and over the telephone with patients
  • Ability to effectively function in stressful situations
  • Ability to keep information confidential
  • Skill in working as a team and as an individual
  • Ability to set priorities, analyze and resolve problems, and make decisions in a timely fashion

 

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