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Science & Research
Clinical Research Coordinator
Cerritos, CA
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Oncology Clinical Research Coordinator II Helios Clinical Research - 3.3 Cerritos, CA Job Details Full-time 2 hours ago Qualifications Laboratory sample storage Record keeping Vital signs Informed consent Logistics management Research ethical considerations Finance Adverse event reporting Clinical incident reports Labeling Operations coordination Filing Phlebotomy specimen handling Mid-level Data summary reports Research project coordination Patient history taking Interview research Bachelor's degree Data management Specimen storage protocols Informed consent procedures implementation Compliance documentation Clinical data report preparation Oncology research Office supply ordering ECG placement Research compliance clinical trial records management Clinical trial patient safety management Implementing research protocols
Full Job Description Job Title :
Clinical Research Coordinator II FSLA Classification :
Non-Exempt Reports to :
CRC Manager Job Summary/ Objective:
The Clinical Research Coordinator II is responsible for supporting the management and oversight of clinical trials. This role involves working closely with a team to ensure the smooth execution of research studies under the guidance of the Site Operations Manager.
Essential Functions Overseeing Clinical Trials:
o Ensure trouble-free running of clinical trials. o Monitor study participants' health throughout the trial. o Compile reports summarizing the success or failure of drugs, technologies, or medical procedures. o Oversee 3-4 trials
Data Collection and Analysis:
o Collect data obtained from research. o Analyze research data.
Participant Interaction:
o Communicate with study participants regarding study objectives. o Administer questionnaires. o Monitor participant adherence to study rules.
Collaboration and Compliance:
o Liaise with laboratories o Monitor study compliance with protocols and ethical standards. o Ensure adherence to regulatory requirements.
Record Keeping:
o Maintain research records, including case report forms and drug dispensation records. o Direct specimen collection, labeling, storage, and transport.
Logistics and Supplies:
o Ensure all necessary equipment and supplies are in stock and functional.
Education/Experience/Skills Education :
Bachelor's degree preferred in health-related field
Experience:
2 years of experience in
Clinical Research Skills:
Regulatory o Filing and accessing documents, Study Submission Assistant, Conduct Close out Visits Finance o Stipend payments Subject Interaction o Recruit, interview, screen, enroll, and randomize subjects o Obtain Informed Consent o Collect medical history o Conduct study visits Administrative o Source documentation o EDC o Query resolution o AE/SAE documentation and reporting o Address protocol violations and deviations o Order supplies Clinical Skills o Phlebotomy o Vital Signs o
ECG Working Conditions/ Physical Demands:
Standard operating hours are Monday through Friday, 8:00 a.m. to 5:00 p.m. May be required to complete job-related tasks outside of that time frame in excess of a standard 40-hour work week. Requires prolonged walking, standing, some bending, stooping, and stretching. Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. Requires normal range of hearing and eyesight to record, prepare, and communicate appropriate reports.
