Clinical research coordinator jobs in Pasadena, CACreate job alerts

Profound Research seeks to drive clinical innovation by partnering with community physicians to offer clinical research as a therapeutic option to their patients. The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, ...

Clinical Research Coordinator I – Data Management (Hybrid). 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 informe...

The Clinical Research Coordinator II serves as the lead coordinator on an assigned portfolio of research studies, functioning independently to establish and coordinate logistics and processes for the conduct of research for the department. Clinical Research Coordinator II - The Angeles Clinic & R...

The Clinical Research Coordinator III 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 process. Responsible for oversight of all studies...

The Clinical Research Coordinator III 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 process. Clinical Research Coordinator III - Guer...

The Clinical Research Coordinator II serves as the lead coordinator on an assigned portfolio of research studies, functioning independently to establish and coordinate logistics and processes for the conduct of research for the department. Clinical Research Coordinator II - The Angeles Clinic & R...

Responsible for oversight of all studies with the group and the assignment of studies to clinical research personnel within the group, and supervision of research staff. Clinical Research Coordinator III - Guerin Children's - Pediatric Neurology & Neurosurgery (Full-Time, On-Site). The Clinical R...

Clinical Research Coordinator II, Per Diem (Onsite) - Gresham Lab. 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 ...

Clinical Research Coordinator I – Data Management (Hybrid). 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 informe...

Clinical Research Coordinator II, Per Diem (Onsite) - Gresham Lab. 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 ...

Clinical Research Coordinator I - Pulmonary Research Program/Lung Institute. The Clinical Research Coordinator I will work independently providing study coordination, screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the inform...

We are seeking a Clinical Research Coordinator to join a community-centered outreach and research team. It combines public health education, participant screening, and mobile unit operations—all with the goal of building equity in clinical research. Travel-based clinical research role with a miss...

The Clinical Research Coordinator II works independently providing study coordination including screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator II – Medically Associ...

The Clinical Research Coordinator II works independently providing study coordination including screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Clinical Research Coordinator II – Medically Associ...

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. Clinical Research Coordinator I - D...

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 consent process. Clinical Research Coordinator I – Data Ma...

Clinical Research Coordinator II, Per Diem (Onsite) - Gresham Lab. 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 ...

The Clinical Research Coordinator II serves as the lead coordinator on an assigned portfolio of research studies, functioning independently to establish and coordinate logistics and processes for the conduct of research for the department. Clinical Research Coordinator II - The Angeles Clinic &

The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader who has direct responsibility for the imple...

The Clinical Research Coordinator I will work independently providing study coordination, screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Maintains research practices using Good Clinical Practice...

The Department of Urology is seeking to hire a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of rese...

The Department of Surgery is seeking a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. The Clinical Research Coordinator collaborates with the Principal Inve...

In addition, the Clinical Research Coordinator is responsible for procuring and distributing study supplies, including coordinating specimen collection and shipping. The Department of Molecular and Medical Pharmacology is seeking a detailed and dynamic Clinical Research Coordinator. In this role,...

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. Maintains research practices using Good Clinical Pr...

The Assistant Clinical Research Coordinator assists the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in contributing to the overall operational management of clinical research/trial/study activities.

Required: * Associates Degree * 3 years of Clinical Research Experience * BLS Preferred: * Bachelors Degree * SoCRA or ACRP Certification * Phlebotomy Certified * Medical Assistant Diploma * Experience with Oncology setting Primary Duties and Responsibilities * Establishes and executes logistical...

Req ID : 9167 Working Title : Clinical Research Coordinator II - The Angeles Clinic & Research Institute Department : Angeles Research Inst Business Entity : Cedars-Sinai Medical Care Foundation Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : EXEM...

The Clinical Research Coordinator I assists Principal Investigators and study team members with research activities such as subject recruitment, data collection, scheduling of study-related activities, and follow-up with enrolled subjects. Certified clinical research associate/coordinator preferr...

Req ID : 8708 Working Title : Clinical Research Coordinator II - Medically Associated Science & Technology (MAST) Program Department : Associated Sci and Tech Program Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Over...

In addition, the Clinical Research Coordinator is responsible for procuring and distributing study supplies, including coordinating specimen collection and shipping. The Department of Molecular and Medical Pharmacology is seeking a detailed and dynamic Clinical Research Coordinator. The role requ...

Req ID : 9171 Working Title : Clinical Research Coordinator II, Per Diem (Onsite) - Gresham Lab Department : Cancer - Research Center Health Equity Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEX...

Req ID : 9528 Working Title : Clinical Research Coordinator III - Guerin Children's - Pediatric Neurology & Neurosurgery (Full-Time, On-Site) Department : Childrens Health Institute Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ ...

Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical research efficiency as needed. Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintena...

Req ID : 7246 Working Title : Clinical Research Coordinator I - Department of Neurology (Hybrid) Department : Research - Neurology Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Primary Shif...

The ideal candidate is an experienced professional who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic...

Req ID : 5003 Working Title : Clinical Research Coordinator I - Pulmonary Research Program/Lung Institute Department : Research - Pulmonary Business Entity : Cedars-Sinai Medical Center Job Category : Academic / Research Job Specialty : Research Studies/ Clin Trial Overtime Status : NONEXEMPT Pri...

You'll work closely with Principal Investigators, co-investigators, our clinical research supervisor, clinical research coordinators, clinics and its staff for each study that you are supporting, along with the Launchpad (HQ) team. If you are passionate about clinical research and want to be part...

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. Knowledge of res...

The Clinical Research Coordinator II serves as the lead coordinator on an assigned portfolio of research studies, functioning independently to establish and coordinate logistics and processes for the conduct of research for the department. Plans and coordinates strategies for growing research par...

ACRP Certified Clinical Research Coordinator (CCRC) or SOCRA Certified Clinical Research Professional (CCRP) required. As a certified research professional, handles clinical trial administration for all protocol phases. Develops procedures related to clinical trial coordination.

As an Assistant Clinical Research Coordinator, you'll play a key role in supporting the management and coordination of clinical trials and research studies. This position offers hands-on experience in a dynamic research environment where your contributions will directly impact the success of clin...

The Clinical Research Coordinator III 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 process. Responsible for oversight of all studies...

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. Maintains research practices using Good Clinical Pr...

RN Clinical Coordinators work collaboratively with multiple departments including but not limited to sterile processing, peer Clinical Coordinators, RNFA's, Charge Nurses (PFC's), and the management team to ensure development and adherence to established departmental policies procedures, standard...

As a Principal Clinical Research Coordinator (PCRC) you will be responsible for serving as a lead within you respective disease team mentoring new staff, providing task level guidance to CRCs and ACRCs, and serving as subject matter experts in key CTO processes. Principal Clinical Research Coordi...

Minimum of 12 months of nursing experience, plus 6 months of specialized experience providing clinical nursing care to dialysis patients, in either a chronic or acute setting. Minimum of 12 months of nursing experience, plus 6 months of specialized experience providing clinical nursing care to di...

The Clinical Research Coordinator I will work independently providing study coordination, screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Maintains research practices using Good Clinical Practice...

Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR. If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites. Minimum one (1) year of training and/or experience in research metho...