Clinical Laboratory Assistant

Job Title:

Clinical Laboratory Assistant Monday through Friday, 7:00 a.m. to 3:30 p.m. •with some flexibility depending on study schedules and operational needs. Job Description Ensures that all clinical trial activities align with study protocols, Good Clinical Practices ( GCP ), and Standard Operating Procedures (SOPs). This role focuses on accepting, documenting, and handling biological samples collected during clinical trials while maintaining strict confidentiality for participants and sponsors. The specialist works both on the clinic floor and in the adjacent laboratory, supporting protocol-driven, time-sensitive study events and contributing to high-quality clinical research operations. Responsibilities + Ensure all assigned tasks comply with study protocols, Good Clinical Practices ( GCP ), and Standard Operating Procedures (SOPs). + Work directly with clinical trial subjects and staff to accept, document, and track biological samples collected during clinical studies. + Handle, process, and store study and clinical diagnostic samples according to protocol-driven timelines and acceptable windows. + Perform protocol-driven timed study events, including but not limited to centrifugation and other sample handling procedures. + Maintain accurate and timely data entry related to sample receipt, processing, storage, and study documentation. + Protect the confidentiality of clinical trial participants and sponsors at all times. + Monitor for procedural deviations, issues, or problems and promptly report them to the appropriate supervisory team members. + Work on the clinic floor and in the laboratory area adjacent to the clinic, adapting to the operational needs of both environments. + Follow all departmental quality standards to maintain a high level of accuracy and reliability in sample handling and documentation. + Collaborate with cross-functional staff to support smooth study execution and resolve operational issues. + Manage multiple tasks and competing priorities while meeting protocol timelines and quality expectations. + Proactively identify study needs and make recommendations for process improvements to management. Required Skills & Experience + High School Diploma or GED required. + 0-3 years of related experience in clinical research, laboratory operations, or a similar field. + Proficiency in data entry with strong attention to accuracy. + Experience or familiarity with clinical research processes. + Basic laboratory skil To view full details and how to apply, please login or create a Job Seeker account