Clinical research coordinator jobs in Pasadena, California - Page 2Create job alerts

Clinical Research Coordinator - Spanish Bilingual. Spanish speaking Clinical Research Coordinator. This is a "boots-on-the-ground" position requiring a blend of clinical expertise and administrative precision.

One (1) year of experience as a Clinical Research Coordinator, Clinical Research Associate, or Clinical Research Assistant preferred. The Clinical Research Coordinator will assist the Research Department with all aspects of clinical research. This position functions as a Clinical Research Coordinato

The Clinical Research Coordinator will be responsible for overseeing clinical trials, obtaining informed consent, adhering to research protocols, maintaining thorough documentation, and ensuring compliance with ethical and regulatory standards. Supported by a skilled team of research assistants, coo

Participant Recruitment & Retention:.Identifies, screens, and recruits eligible subjects; obtains informed consent.Schedules patient visits, conducts study procedures, and ensures protocol adherence.Collects, records, and manages source data; completes Case Report Forms (CRFs) and resolves queries.M

The Clinical Research Budget Coordinator II develops complex clinical trial budgets for industry, National Institutes of Health (NIH), and investigator-initiated clinical research. To be considered for the Clinical Research Finance Coordinator II (Pre-Award) position, applicants must have direct exp

Key Responsibilities * Coordinate and execute clinical trials in compliance with protocol, GCP, and regulatory requirements * Screen, enroll, consent, and follow study participants per SOPs * Perform clinical procedures including phlebotomy, vitals, and ECGs * Identify and report AEs/SAEs promptly

Clinical Research Coordinator - Spanish Bilingual. Spanish speaking Clinical Research Coordinator. This is a boots-on-the-ground position requiring a blend of clinical expertise and administrative precision.

Participant Recruitment & Retention:.Identifies, screens, and recruits eligible subjects; obtains informed consent.Schedules patient visits, conducts study procedures, and ensures protocol adherence.Collects, records, and manages source data; completes Case Report Forms (CRFs) and resolves queries.M

Clinical research coordinators are responsible for conducting clinical research trials by adhering to Good Clinical Practice (GCP), International Air Transportation (IATA) and FDA regulations. Clinical research coordinators need to engage with the research investigators, pharmaceutical companies (sp

PIH Health is seeking a Clinical Research Coordinator in South El Monte, California. This role involves managing and coordinating clinical research studies, ensuring compliance with regulatory requirements, and working closely with principal investigators and research staff. Candidates should posses

Are you ready to be a part of breakthrough research? The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non‑medical trial concepts and details, and participating in the informed conse

A leading university health system in Los Angeles is seeking a Regulatory Coordinator to oversee all regulatory documentation for clinical research in the urology department.

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. Candidates should have at least one year of clinical research experience and a high school diploma.

Job Description:**Clinical Research CoordinatorThe Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent proce

Hands‑on experience in lab courses, research projects, or clinical settings (internships, volunteering, or academic labs) Strong attention to detail and the ability to follow structured protocols Excellent organizational and time management skills Clear communication skills and comfort interact

These locations are formerly Valkyrie Clinical Trials - we are proud to welcome Valkyrie Clinical Trials to the Flourish Research network! The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating

Overview The Clinical Research RN Coordinator position works collaboratively with investigator(s) and assists with formulating clinical research objectives, contributes to the design of clinical research protocols, oversees clinical research trials, and conducts quality assurance reviews. Responsib

A clinical research organization in Pasadena is seeking a Clinical Research Coordinator to manage trial activities while ensuring compliance with regulations and protocols. Join us to make a significant impact in clinical research. The ideal candidate will possess a relevant degree and experience in

Dermcare Management Llc in Los Angeles seeks a Clinical Research Coordinator responsible for overseeing clinical trials, ensuring regulatory compliance, and engaging with subjects. Join us to make a difference in clinical research.

Are you ready to be a part of breakthrough research? The Clinical Research Coordinator I works independently to coordinate studies and screen candidates to determine protocol eligibility. Licenses and Certifications: Certification in Clinical Research from SOCRA or ACRP certification is preferred.

Actalent is seeking a Clinical Research Coordinator (Bilingual – English/Spanish) to manage clinical trials and ensure adherence to regulatory standards. The position provides meaningful patient impact while supporting a collaborative clinical research environment.

Job Description The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. They compile and report on each study,

The Senior Clinical Research Coordinator oversees the operational management of clinical research studies from start-up through closeout. Key Responsibilities: Manage day-to-day operations for one or more clinical research studies, including multicenter and investigator-initiated trials Ensure stu

Children's Hospital Los Angeles (CHLA) is looking for a Clinical Research Coordinator II in Los Angeles, California. The role involves coordinating clinical research protocols, managing specimen collections, assisting with data extraction, and ensuring compliance with regulatory requirements. Applic

A leading cancer care provider in Glendale, CA, is seeking a Clinical Research Coordinator to manage study coordination, ensure compliance with regulatory standards, and enhance patient enrollment strategies. The ideal candidate will have at least 1 year of clinical research experience and a preferr

A leading healthcare institution in Los Angeles is seeking an experienced Clinical Research Coordinator II to manage clinical trials and assure adherence to regulatory frameworks. Candidates should possess a high school diploma, with a preference for a degree in a related field, alongside certificat

The Clinical Research RN Coordinator position works collaboratively with investigator(s) and with formulating clinical research objectives, contributes to the design of clinical research protocols, oversees clinical research trials, and conducts quality assurance reviews. Preferred Experience: 2 yea

Responsibilities Provide clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data; Attend

This role involves collaborating with investigators to formulate clinical research objectives, overseeing clinical research trials, addressing patient complaints, and scheduling testing and treatments according to protocols. Keck Medicine of USC is seeking a Clinical Research RN Coordinator in Arcad

Key Responsibilities Manage day‑to‑day operations for one or more clinical research studies, including multicenter and investigator‑initiated trials Ensure study protocols and procedures are carried out accurately, safely, and on schedule Coordinate timelines, prioritize tasks, and support

Position Overview: The Greater Los Angeles Veterans Research and Education Foundation (GLAVREF) seeks an enthusiastic Clinical Research Coordinator (CRC) to join our dynamic clinical trials team. Overview EXPERIENCED Clinical Research Coordinator - Onsite Job Details: 15-20 hours/week for the f

The Senior Clinical Research Coordinator oversees the operational management of clinical research studies from start-up through closeout. Key Responsibilities Manage day-to-day operations for one or more clinical research studies, including multicenter and investigator-initiated trials Ensure stud

The Clinical Research Coordinator (CRC) is responsible for managing and coordinating clinical research studies conducted in a hospital setting, ensuring compliance with regulatory requirements and institutional policies. Certification as a Clinical Research Coordinator (e. Minimum 2‑3 years of exp

Hands‑on experience in lab courses, research projects, or clinical settings (internships, volunteering, or academic labs) Strong attention to detail and the ability to follow structured protocols Excellent organizational and time management skills Clear communication skills and comfort interact

The ideal candidate will coordinate study assessments, assist with participant recruitment and informed consent, and engage in data collection and compliance with research protocols.

Qualifications: 2–5 years of Clinical Research Coordinator experience in a physician practice or private research setting. We are specifically seeking candidates with hands‑on Clinical Research Coordinator experience within physician office or private practice clinical trial settings. Job Descr

Responsibilities Coordinate and schedule study assessments, procedures, and activities to ensure compliance with research protocols and timelines. Collect, document, and enter research data according to established protocols. Perform initial data analysis under the guidance of senior coordinators o

The Consumer Insights Division of our organization is expanding its nationwide research team. No previous market research or industry experience required. Participate in nationally recognized research initiatives.

Upon successful completion of the research study your compensation will be issued via a Check, Paypal, Visa gift card or other form of compensation. Part-time Research Study Personnel (Pay up to $790/wk. Due to demand, we are now accepting applications for personnel to participate in our local in-pe

Remote Work From Home Administrative Assistant Admin - Part Time Market Research Panelists Our company is seeking individuals to participate in National & Local Paid Focus Groups, Clinical Trials, and Market Research assignments. Seeking participants for Focus Group and market research studies.