Clinical Research Study Assistant II - Medical Oncology

About the role

Under direction, participates in clinical research study activities; screens, obtains consent, and enrolls participants in study; performs a variety of duties involved in the collection, documentation, and reporting of clinical research data.

Primary Duties & Responsibilities

• Participates in the recruitment of study participants as identified in related protocol; visits with study participants to explain study, screens for eligibility and obtains informed consent of participants.
• Completes all necessary paperwork/documentation according to study protocol; obtains consent, interviews study subjects and schedules follow-ups as needed.
• Performs basic/scripted assessments to confirm eligibility to participate in study; explains and schedules laboratory and diagnostic procedures and/or treatment as required in the study; refers participants to basic resources as necessary.
• Collections data from study participants, medical records, interviews, questionnaires, diagnostic tests and other sources; performs basic evaluation and interpretation of collected data and prepares appropriate reports and documentation as necessary; prepares and distributes study packets and information.
• Performs other duties as assigned.

Working Conditions

Job Location/Working Conditions Normal office environment
Physical Effort Typically sitting at desk or table
Repetitive wrist, hand or finger movement
Equipment Office equipment

Education

Required Qualifications: High school diploma or equivalent high school certification or combination of education and/or experience.

Preferred Qualifications

Associate degree

Work Experience

Administrative Or Research (2 Years)

Skills

Interpersonal Communication, Oral Communications, Organizing, Written Communication

Additional Information

Basic Life Support certification must be obtained within one month of hire date