Clinical Research Technician I (CPT or MA)

CareAboutCypress, CA
4d$19 - $21

About The Position

At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. About The Role The Clinical Research Technician I will work with Clinic Operations teams to execute clinical trial activities. Responsibilities of the Clinical Research Technician I include execution of What You'll Do Here/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.

Requirements

  • Certified Phlebotomy Certificate or MA Diploma required, along with a BLS
  • High School Diploma or GED required; college degree and related work experience preferred.
  • Good communication, customer service focus, and ability to work in a fast-paced environment.

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 not limited to, sample handling, safety measurements, 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
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service