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Clinical Research Coordinator - Oncology

Helios Clinical Research
Cerritos, CA Full Time
POSTED ON 4/22/2026
AVAILABLE BEFORE 10/18/2026

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. 


Travel required: as needed (travel to IM’s may be required


Pay ranges between $28-$31 hourly

Salary : $28 - $31

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