Clinical Research Coordinator - Oncology

Helios Clinical Research; Cerritos (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

Helios Clinical Research in Cerritos, California is seeking a Clinical Research Coordinator II to support management of clinical trials. The role involves working closely with a team to ensure successful execution of research studies, overseeing trial operations, and maintaining compliance with protocols.

Ideal candidates will have at least 2 years of clinical research experience and a Bachelor's degree in a health-related field. Skills in data analysis and patient interaction are essential.

Qualifications

• 2 years of experience in Clinical Research.
• Must have previous Oncology and on-site direct patient interaction experience.

Responsibilities

• Oversee clinical trials ensuring smooth execution.
• Collect and analyze data from research.
• Liaise with laboratories and ensure protocol compliance.
• Maintain research records and supply logistics.

Skills

Filing and accessing documents

Clinical data collection

Understanding of ethical standards

Conduct study visits

Vital Signs

ECG

Education

Bachelor's degree in health-related field

Job description

*MUST have previous Oncology and on-site direct patient interaction experience

Job Title

Clinical Research Coordinator II

FSLA Classification

Non-Exempt

Reports to

CRCManager

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
  • Ensure trouble-free running of clinical trials.
  • Monitor study participants’ health throughout the trial.
  • Compile reports summarizing the success or failure of drugs, technologies, or medical procedures.
  • Oversee 3-4 trials.
• Data Collection and Analysis
  • Collect data obtained from research.
  • Communicate with study participants regarding study objectives.
  • Monitor participant adherence to study rules.
• Collaboration and Compliance
  • Liaise with laboratories.
  • Monitor study compliance with protocols and ethical standards.
  • Ensure adherence to regulatory requirements.
  • Maintain research records, including case report forms and drug dispensation records.
  • Direct specimen collection, labeling, storage, and transport.
• Logistics and Supplies
  • 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:
  • Filing and accessing documents, Study Submission Assistant, Conduct Close out Visits.
  • Stipend payments.
  • Recruit, interview, screen, enroll, and randomize subjects.
  • Collect medical history.
  • Conduct study visits.
  • EDC.
  • Query resolution.
  • AE/SAE documentation and reporting.
  • Address protocol violations and deviations.
  • Order supplies.
• Clinical Skills:
  • Vital Signs.
  • 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).