Job Description

Job Description

Preferred qualifications include demonstrated experience in accurately processing research laboratory specimens in accordance with study protocols and standard laboratory procedures. This includes tasks such as centrifugation, aliquoting, proper storage, and shipment of samples. Candidates with this experience are strongly encouraged to apply.

This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time.

This position functions as a Clinical Research Coordinator providing support for clinical research protocols for the department. The Clinical Research Coordinator will assist the Research Department with all aspects of clinical research. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all regulatory requirements.

Primary Duties & Responsibilities

• Perform accurate processing of research laboratory specimens while demonstrating a moderate degree of proficiency and understanding of research protocol and laboratory procedures, including centrifuging, aliquoting, storing, and shipping of specimens.
• Monitor deliveries from sponsor, including inventory of kits, unpacking, and storing of supplies, and utilizing kits and supplies appropriately for specimen collection, processing, storage, and shipping, as mandated by sponsor. Maintain electronic record of supplies.
• Responsible for administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE’s and source documents.
• Facilitates screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
• Coordinates logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
• Responsible for accurate and timely data collection, documentation, entry and reporting, including timely response to sponsor queries.
• Schedules and participates in monitoring and auditing activities to ensure compliance, including implementing any corrective actions.
• Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
• Works closely with investigators and regulatory staff or directly with Institutional Review Board (IRB) to submit adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
• Acts as a liaison with pharmaceutical company representatives or other project funding organizations to monitor and update project progress.
• Provides assistance with research finance billing, including identifying and classifying routine care vs. research related care.
• Attends meetings and conferences related to research activities, including research staff meetings. Participates in planning, workshops,evaluation meetings, and seminars, educational or administrative meetings as necessary or requested.

Qualifications

Job qualifications

• High School Diploma/GED required.
• 6 months of Healthcare related or research experience.
• 1 year of experience as a clinical research coordination or clinical research associate/assistant.
• Phlebotomy and lab assistant experience with demonstrated competency in the job duties listed above
• Phlebotomy Certification from State of California, please note your license number in your resume.
• Basic Life Support (BLS). Must be issued by American Heart Association and you can receive within 60 days of hire.

Preferred qualifications include demonstrated experience in accurately processing research laboratory specimens in accordance with study protocols and standard laboratory procedures. This includes tasks such as centrifugation, aliquoting, proper storage, and shipment of samples. Candidates with this experience are strongly encouraged to apply.

This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time.

Preferred Job Requirements:

• Associate Degree/Colllege Diploma preferred.
• Demonstrated ability to accurately process research laboratory specimens in accordance with study protocols and standard laboratory procedures. This includes centrifugation, aliquoting, proper storage, and shipment of specimens.
• Moderate level of proficiency in understanding and adhering to research protocols and laboratory safety guidelines.
• Experience monitoring and receiving study-related deliveries from sponsors, including performing inventory checks, unpacking, and storing of kits and supplies.
• Ability to properly utilize sponsor-provided kits and supplies for specimen collection, processing, storage, and shipping as outlined in protocol requirements.
• Proficient in maintaining electronic records of inventory and supplies to ensure adequate stock and traceability.

Req ID : 10430
Working Title : Clinical Research Coordinator I, Laboratory (Onsite) + CPT, Angeles Clinic
Department : Angeles Research Inst
Business Entity : Cedars-Sinai Medical Center
Job Category : Academic / Research
Job Specialty : Research Studies/ Clin Trial
Overtime Status : NONEXEMPT
Primary Shift : Day
Shift Duration : 8 hour
Base Pay : $26.64 - $41.29

Job Tags

Full time, Local area, Shift work,

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