Clinical Research Coordinator I – Neurology Trials

Cedars-Sinai; Los Angeles (CA); Sur place; USD 32 222 - 54 773; Plein temps

Résumé du poste

A leading medical center in Los Angeles is seeking a Clinical Research Coordinator I to support research programs in the Department of Anesthesia and Neurology. The role requires scheduling participants, documenting data, and ensuring compliance with regulations. Candidates should have at least one year of clinical research experience and a high school diploma. A bachelor's degree is preferred, along with ACRP/SOCRA certification. Competitive hourly pay ranges from $23.39 to $39.76.

Qualifications

• 1 year of clinical research experience required.
• ACRP/SOCRA certification preferred.

Responsabilités

• Schedule research participants for visits.
• Document changes in participant condition.
• Notify about data quality concerns.
• Maintain patient confidentiality.

Connaissances

Clinical research experience

Data collection

Documentation

Good Clinical Practice (GCP)

Formation

High School Diploma/GED

Bachelor's degree in Science or related field

Description du poste

Job Description

Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!

Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world. Ranked among the best in the nation by U.S. News & World Report, our neurosurgeons and neurologists work together with experienced care teams to give patients the most effective treatment possible.

About the Role

This position will support the research programs in Department of Anesthesia and Neurology.

The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The CRC I member is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. This role is responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The incumbent presents study information at research staff meeting. This position ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board.

Primary Duties and Responsibilities:

• Scheduling of research participants for research visits and procedures.
• In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) information about changes in research participant condition, adverse events, concomitant medication use, protocol compliance, and response to study drug.
• Schedules and participates in monitoring and auditing activities.
• Notifies direct supervisor about concerns regarding data quality and study conduct.
• Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters following local and federal guidelines.
• May perform other regulatory/Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.
• Maintains research practices using Good Clinical Practice (GCP) guidelines.
• Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
• Participates in required training and education programs.
• Coordinates training and education of other personnel.

Department-Specific Duties and Responsibilities:

• Transportation of research medications.
• Performs research study related assessments and questionnaires.
• Assists with prescreening of research participants for various clinical trials.
• Attends research meetings and monthly conference calls with sponsors for study updates.
• Maintains organized paper and electronic research files.
• Performs all data collection and data entry tasks for department clinical trials.
• Assists with preparing manuscripts, letters, and other research documents as needed.
• Responds to sponsor’ inquiries regarding protocol start-up activities and recruitment.
• Performs literature reviews.

Qualifications

Education:

• High School Diploma/GED, required.
• Bachelor's degree in a Science, Sociology, or related field is preferred.

Licenses/Certifications:

• ACRP/SOCRA certification is preferred.

Experience:

• 1 year of clinical research experience, required.