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Oncology Clinical Research Coordinator III Helios Clinical Research - 3.3 Cerritos, CA Job Details Full-time 2 hours ago Qualifications Incident reporting compliance Record keeping Laboratory project records management Medical procedure preparation Informed consent Patient monitoring Logistics management Finance Pre-examination patient preparation Adverse event reporting Clinical incident reports Materials management in healthcare Labeling Triage Filing Phlebotomy specimen handling Mid-level ECG equipment 3 years Research project coordination Patient history taking Bachelor's degree Clinical data entry Team training Clinical information systems Adverse drug reaction monitoring Informed consent procedures implementation Clinical assessment documentation Oncology research Data entry

Full Job Description Job Title:

Clinical Research Coordinator III- Oncology FSLA Classification:

Non-Exempt Reports to:

CRC Manager Job Summary/ Objective:

The Clinical Research Coordinator III 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 Investigator and CRC Manager.

Essential Functions:

Overseeing Clinical Trials:

Ensure smooth conduct of study visits and clinical trials. Monitor study participants' health throughout the trial. Schedule study visits within protocol-required timelines Coordinate lab work, imaging, and other required procedures Document all aspects of the study visit and subject status.

Data Collection and Analysis:

Collect and enter data obtained from study visits into source documents, study logs, and EMR, as well as EDC where data management personnel are not assigned. Assist data management team with resolution of queries

Participant Interaction:

Educate study participants about study objectives and visit procedures. Communicate with study participants regarding any adverse events or side effects and the management of them. Administer applicable questionnaires. Monitor participants' adherence to protocol guidelines.

Collaboration and Compliance:

Liaise with laboratories Liaise with Imaging vendors Liaise with pharmacy staff and infusion nurses Liaise with regulatory and quality assurance departments on protocol adherence and documents. Monitor study compliance with protocols and ethical standards. Ensure adherence to regulatory requirements.

Record Keeping:

Maintain research records, including source documents, study logs, case report forms, and EMR Direct specimen collection, labeling, packaging, transport, shipping, and storage.

Logistics and Supplies:

Ensure all necessary equipment and supplies are in stock and functional.

Education/Experience/Skills:

Education:

Bachelor's degree preferred in a health-related field

Experience :

+3 years of experience in

Clinical Research Skills:

Regulatory Filing and accessing documents, Study Submission Assistant, Conduct Close-out Visits Report protocol deviations and SAEs to the IRB (where not performed by the Research Navigator) Finance Stipend payments Manage site budgets Insurance Coordination Subject Interaction Recruit, interview, screen, enroll, and randomize subjects Obtain Informed Consent Collect medical history Conduct study visits Triage patients' questions Administrative Source documentation EDC completion Query resolution AE/SAE documentation and reporting Address protocol violations and deviations Order/ maintain supplies Clinical Skills Phlebotomy preferred Vital Signs EKG Order and organize lab reports IP Administration Manage Medical Records Others Support training and answer questions of other staff members Support monitoring visits Leads sponsor communication Manage subject visits during managers' absence Liaise with Investigators in manager's absence

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 more than a standard 40-hour work week. Requires prolonged walking, standing, bending, stooping, and stretching. Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. Requires a normal range of hearing and eyesight to record, prepare, and communicate appropriate reports. Travel required : as needed (travel to IMs may be required) Disclaimer This job description may not be inclusive of all assigned duties, responsibilities, or aspects of the job described, and may be amended at any time at the sole discretion of the Employer.