Clinical Research Study Assistant II - Obstetrics and Gynecology

About the role

Under the direction of a Research Coordinator or PI, participates in clinical research study activities; screens, obtains consent, and enrolls 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