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ROLE SUMMARY

  • Assists in the conduct of clinical research studies or trials following established protocols and standard operating
    procedures; prepares and organizes space; sets up study-related equipment and supplies. Assists with routine data
    collection to support clinical research (such as documenting vital signs, performing phlebotomy, etc.)

FUNDAMENTAL RESPONSIBILITIES

  • Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures; prepares and organizes space; sets up study-related equipment and supplies.
  • Sets up and monitors various research study protocols, such as data collection efforts.
  • Assists with routine data collection to support clinical research (such as documenting vital signs, performing phlebotomy, etc.).
  • Schedules/calls subjects for appointments as directed; obtains screening information via phone or in person from script template for minimal risk studies; records and maintains screening/enrollment/master subject logs.
  • Ensures proper recording and archival of all regulatory documents, including informed consent forms for submission to regulatory agencies; files all appropriate correspondence
    Provides other various support for clinical research efforts (makes copies, prepares transmittal sheets for mailings, sends out various resources/information).\

QUALIFICATIONS
EDUCATION

  • Undergraduate or Graduate Work-Study Students
    Required:
  • High School Diploma or equivalent (such as HSED or GED)

PHYSICAL & MENTAL DEMANDS

  • The role regularly requires the ability to effectively communicate.
  • The role frequently requires the ability to move about the work environment and to position oneself to operate laboratory equipment effectively.
  • The role requires the ability to move objects weighing up to 25 pounds and will occasionally work near moving mechanical parts.
  • The person in this role must be able to perform the essential functions with or without an accommodation.