University of CA, Riverside School of MedicineRiverside, 21 mi from Irvine
excellence in clinical research with an emphasis on advanced cardiac imaging and structural heart disease assessment and guidance. The successful candidate for this position should also demonstrate notable scientific contributions and a track record...
Allergan AestheticsIrvine
Job Description
The Toxin Innovation Group at AbbVie seeks an accomplished scientist and leader for the Toxin Innovation Pharmacology Group. The Associate Director/ Principal Research Scientist II will lead discovery research activities to generate...
Ampcus IncorporatedLos Angeles, 32 mi from Irvine
DURATION: 12 weeks with possible hire SHIFT:M-F 8-5 REQUIRED EXP: Min 2 yrs exp in a clinical research coordinator role, College Degree, exp with IRB procedures, recruiting and enrolment, completing CRFs
Clinical Research Associate
Location: Los...
CEDARS-SINAILos Angeles, 32 mi from Irvine
of medical advancements!
The Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study.
The CRAI evaluates...
Belmont VillageAliso Viejo
Freedom Lane, Aliso Viejo, CA 92656.Hiring PRN or On-call Caregivers/CNAs - $19-$21/hour .Instant Access to Wages Before Payday, Flexible scheduling, Meals Provided, Excellent Benefits & Paid Time Off available (Full-Time employees).Is Belmont Village a Good Match for You?.Belmont Village e...
Belmont VillageAliso Viejo
BELMONT VILLAGE ALISO VIEJO .Freedom Ln, Aliso Viejo, CA 92656.Hiring Part-Time Receptionist/Concierge.Friday and Saturday 7:30am-3:30pm.Prior Experience with multi-line phone system and exceptional customer service skills are required.Excellent position for a second act career or for those who...
Belmont VillageAliso Viejo
BELMONT VILLAGE ALISO VIEJO .Freedom Ln, Aliso Viejo, CA 92656.Hiring Part-Time Receptionist/Concierge.Friday and Saturday 7:30am-3:30pm.Prior Experience with multi-line phone system and exceptional customer service skills are required.Excellent position for a second act career or for those who...
Advanced Nutrients Ltd.Irvine
University of California Irvine
Dermatology Faculty Health Science Clinical (Open Ranks)
Health Sciences Clinical Professor Series, Open Ranks
Department of Dermatology, UC Irvine
The Department of Dermatology at the University of California...
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Clinical Research Associate
SGA Inc. | Los Angeles | www.resume-library.com |
Software Guidance & Assistance, Inc., (SGA), is searching for a Clinical Research Associate for a CONTRACT assignment with one of our premier Healthcare clients in Los Angeles, CA .
Responsibilities : The Department of Medicine Clinical Trial Program is seeking a skilled Clinical Research Associate to oversee, manage and participate in research activities. Providing oversight of clinical research sites compliance with ICH/Good Clinical Practices (GCP), governing SOPs (standard operating procedures) and clinical study protocols.
This includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Responsible for regulatory coordination of clinical research studies, preparation, submission and maintenance of regulatory files to fulfill research requirements.
Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members.
Work may be assigned by Senior Management, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. Travel to other locations may be required.
Required Skills:
A multi-tasked individual with a minimum 2 years of experience in a clinical research coordinator role.
College degree in medicine, science, health, or equivalent.
Performs management of research activities to ensure the collection of accurate clinical data within given timeline.
Knowledge of ICG GCP guidelines and expertise to review, evaluate medical data and all applicable local laws and regulations.
Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc
Experience in selection and management of vendors/CROs (Central Lab, IVRS, EDC)
Track progress of clinical studies with regard to budget, study milestones, and deadlines.
Recruiting & enrolment of patients who meet eligibility criteria, scheduling, completing CRFs.
Able to solve complex problems, prioritize multiple tasks, plan proactively and accomplish goals within project in a dynamic team environment
Participate in study audits, as applicable
SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements.
When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work.
Please find us at .
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status.
We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
Responsibilities : The Department of Medicine Clinical Trial Program is seeking a skilled Clinical Research Associate to oversee, manage and participate in research activities. Providing oversight of clinical research sites compliance with ICH/Good Clinical Practices (GCP), governing SOPs (standard operating procedures) and clinical study protocols.
This includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Responsible for regulatory coordination of clinical research studies, preparation, submission and maintenance of regulatory files to fulfill research requirements.
Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members.
Work may be assigned by Senior Management, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. Travel to other locations may be required.
Required Skills:
A multi-tasked individual with a minimum 2 years of experience in a clinical research coordinator role.
College degree in medicine, science, health, or equivalent.
Performs management of research activities to ensure the collection of accurate clinical data within given timeline.
Knowledge of ICG GCP guidelines and expertise to review, evaluate medical data and all applicable local laws and regulations.
Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc
Experience in selection and management of vendors/CROs (Central Lab, IVRS, EDC)
Track progress of clinical studies with regard to budget, study milestones, and deadlines.
Recruiting & enrolment of patients who meet eligibility criteria, scheduling, completing CRFs.
Able to solve complex problems, prioritize multiple tasks, plan proactively and accomplish goals within project in a dynamic team environment
Participate in study audits, as applicable
SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements.
When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work.
Please find us at .
SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status.
We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company to request an accommodation or assistance regarding our policy.
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