Clinical Research Assistant II - Tisch Cancer Center

Responsibilities

• Provides organizational, administrative and clinical assistance for the Multiple Myeloma research study program such as preparing and coordinating meetings with various departments and personnel, assist in invoice and payment resolution
• Performs activities in accordance with established policies and procedures related to clinical research study protocols, including but not limited to: answering phone calls, scheduling appointments, coordinating specimen collection, assist with data entry, and review of safety reports.
• Collections and records study data. Inputs all information accurately into database.
• Aids in preparing grant applications, IRB/GCO for submission and filings.
• Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews.
• Secures, delivers and ships clinical specimens as required by the protocol. Collects and processes specimens and point of care testing, prepares for exam, etc.
• Aids clinicians with various procedures, takes vital signs, relays instructions to patients and or families; answers calls and provides pertinent information.
• Performs other related duties.

  Qualifications

  • Associates Degree in related field or HS Diploma with equivalent related experience
  • 2 years in research environment preferred
  • Preferred: Excellent written and oral communication skills Exceptional attention to detail and accuracy Ability to juggle multiple tasks and schedules