Clinical Research Technician I (CPT or MA)

Altasciences•Cypress, CA

1d•Onsite

About The Position

The Clinical Research Technician I will be working with the Clinic Operations teams to execute clinical trial activities. Responsibilities of the Clinical Research Technician I include execution of tasks performed/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). This is a variable hour position.

Requirements

Current Certified Phlebotomy Technician license Or a current Medical Assistant (MA or CMA) certification is required
Current Basic Life Support (BLS, CPR/AED) certification, required
High School Diploma or GED required.

Responsibilities

Ensure the confidentiality of clinical trial participants and sponsors is respected.
Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
Report procedural deviations to appropriate supervisory team members.
Preparation and proper clean-up of applicable workstations (i.e. urine collection station, blood processing station, etc.).
Maintain and advocate a high level of customer service, quality and safety within the department.
Perform clinical trial activities may include but are not limited to sample handling, safety measurements, meals distribution, in-house testing and questionnaire administration.
Conduct all clinical trial activities and participant interaction with a high standard of customer service.
Report significant participant misbehavior to Study/Clinical Operations management teams.
Provide feedback, where necessary, to appropriate team members of study progress.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
Complete and/or maintain training as required per jobs needs.
Other tasks as assigned by management.