Clinical Research Assistant

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.