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clinical research associate Jobs in Los Angeles

clinical research associate

clinical research coordinator Jobs in Los Angeles

clinical research coordinator

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assistant clinical research coordinator pediatrics

UCLA Health

<div><div>Description
The Assistant Clinical Research Coordinator (CRC) will join a centralized clinical research team conducting clinical trials across multiple pediatric sub-specialties. Under the direction of the Clinical Research Supervisor, the Assistant CRC will support team members with activities including data entry, query resolution, document management, and specimen handling.
This role assists in planning and organizing study-related tasks to ensure compliance with study protocols and applicable regulations. The Assistant CRC must be adaptable, able to manage shifting priorities, and willing to work flexible hours to meet research deadlines. Travel to other locations may be required. This position is primarily on-site at the UCLA Westwood campus.
This is a limited position that may convert to career.
Salary Range: $29.28 - $47.10 Hourly</div><div> 
Qualifications
Required:
<ul>
<li>Ability to work efficiently and complete tasks with thoroughness and accuracy.</li>
<li>Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build relationships.</li>
<li>Strong organizational capabilities.</li>
<li>Skills sufficient to solve problems and identify solutions.</li>
<li>Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.</li>
<li>Ability to respond to situations in an appropriate and professional manner.</li>
<li>Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.</li>
<li>Ability to be flexible in handling work delegated by more than one individual.</li>
<li>Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry.</li>
<li>Ability to navigate numerous software programs and applications.</li>
<li>Ability to handle confidential material information with judgement and discretion.</li>
<li>Skill in coordinating information transfer among multiple constituents.</li></ul> 


Preferred:
<ul>
<li>Experience in a Health Care Setting.</li></ul></div></div>

Assistant Clinical Research Coordinator - Pediatrics

<div><div>Description
The Department of Medicine, Division of Cardiology, is seeking a Research Nurse Coordinator to support cardiovascular clinical trials and innovative research initiatives. Under the direction of the Principal Investigator, this role performs independent nursing and advanced administrative duties to ensure the effective implementation and management of clinical research protocols. Responsibilities include seeing research participants, reviewing safety labs and adverse events, implementing investigational drug dose adjustments per protocol, and performing specialized clinical procedures such as electrocardiograms, spirometry, and cardiopulmonary exercise testing while monitoring vital signs.
This position supports a diverse portfolio of studies, including multicenter NIH and industry-sponsored trials, investigator-initiated research, and programmatic activities such as clinical databases and biorepositories. The Research Nurse Coordinator works closely with investigators, clinicians, research staff, and external partners to ensure regulatory compliance, patient safety, and efficient study operations while contributing clinical expertise to the advancement of cardiovascular research.
*This is a limited role which may convert to career.*
Hourly range: $70.59-$106.80</div><div>
Qualifications
<div>Required:</div><div></div><ul><li>
BSN or MSN &ndash; required</li><li>
Active California Registered Nursing License</li><li>
5 years of Cardiovascular Research experience</li><li>
ACLS, BCLS and PALS from the American Red Cross or American Heart Association &ndash; required</li><li>
Ability to complete a Nursing physical assessment</li><li>
Ability to conduct cardiopulmonary exercise testing</li><li>
Ability to complete research case report forms and other research-related documentation according to good clinical practice (GCP) standards and regulatory requirements</li><li>
Ability to follow research standard operating procedures and study protocols</li><li>
Working knowledge of HIPPA guidelines and Human Subjects Protection rights.</li></ul></div></div><div></div>

Research Nurse Coordinator (20% Limited)

<div><div>Description
The Clinical Research Coordinator will join a centralized clinical research team conducting clinical trials across multiple pediatric sub-specialties. Under the direction of the Clinical Research Supervisor, the Clinical Research Coordinator will manage and coordinate clinical trial activities.
Responsibilities include, but are not limited to, participant recruitment, assessment of trial eligibility, enrollment, coordination of research visits, collection and management of participant source documents, regulatory submissions and file maintenance, data management, and specimen handling. The Clinical Research Coordinator is responsible for adhering to institutional and federal clinical research requirements and ensuring studies are conducted in accordance with study protocols and Good Clinical Practice.
This role requires the ability to adapt to changing priorities and work flexible hours to meet research deadlines. Travel to other locations may be required. This position is primarily on-site at the UCLA Westwood campus.
This is a limited position that may convert to career.
Salary Range: $36.37 - $58.52 Hourly
</div><div>Qualifications
Required:<ul><li>
Bachelor&rsquo;s degree or 2+ years of previous study coordination or clinical research coordination experience</li><li>
Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators, and administration and to work as a member of a team.</li><li>
Ability to effectively communicate and interact with patients in a compassionate and kind manner.</li><li>
Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.</li><li>
Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.</li><li>
Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.</li><li>
Organization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met.</li><li>
Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.</li><li>
A learning and professional growth mentality so that new software tools, systems, and processes can be adopted quickly and efficiently.</li><li>
Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.</li><li>
Strong verbal and written communication skills to effectively establish rapport, building collaborative relationships, and communicate complex concepts and ideas in an easy-to-understand manner.</li><li>
Ability to adapt to changing job demands and priorities, remain flexible including working flexible hours to accommodate research deadlines.</li><li>
High degree of concentration and focus on a work environment that contains distracting stimuli, competing deadlines, and work delegated by more than one individual.</li><li>
Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc.</li></ul>
Preferred:<ul><li>
Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.</li></ul></div></div>

Clinical Research Coordinator - Pediatrics

<div><div>Description
Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Health&rsquo;s world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.

The Study Coordinator supports the full operational lifecycle of clinical research studies&mdash;from initial design and start‑up through conduct and closeout. This role is responsible for implementing study activities for one or more protocols, managing day‑to‑day tasks, and prioritizing work to meet project deadlines. The incumbent ensures strict adherence to study protocols, institutional policies, FDA regulations (CFR), and ICH Good Clinical Practice (GCP) standards.

Salary: $36.37 - $58.52 hourly 
 
</div><div>Qualifications
Required:<ul><li>
Bachelors Degree or equivalent experience/training 
</li><li>
Minimum 3 years of related experience or training 
</li><li>
Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships. 
</li><li>
Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness. 
</li><li>
Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines. 
</li><li>
Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications. 
</li><li>
Working knowledge of Institutional Review Board review and reporting requirements, institutional committee application and approval process, Contracts and Grants and departmental policies and procedures. Working knowledge of Institutional Review Board and Internal Scientific Peer Review Committee. 
</li><li>
Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets. 
</li><li>
Working knowledge of FDA Code of Federal Regulations and ICH good clinical practices for clinical research.</li></ul></div></div>

Clinical Research Coordinator - Radiological Sciences

TRIO - Translational Research in Oncology

<div>
 If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!
 
 
 Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.
 
 
 TRIO is looking for a CRA to join our Monitoring Resources team in the USA. This position will be remote, based out of the West Coast, and will require travel.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects
 </li>
 <li>
 Conduct Pre-Study Site Visits (or calls), Study Initiation Visits, Routine Monitoring Visits and Site Close-out at assigned clinical study sites as per TRIO SOPs/SGs/IMs and study- specific SGs/IMs
 </li>
 <li>
 Perform source document verification, validate Case Report Forms (CRFs) and perform query resolution in a timely manner to ensure clean data availability for studies analyses
 </li>
 <li>
 Input and maintain study information in tracking systems: Provide regular/accurate sites status updates and common site trends to Monitoring Resources and Project Management Departments
 </li>
 <li>
 Oversee study drug management at clinical study sites (availability, receipt, handling, storage, dispensation, tracking and accountability, and destruction/return)
 </li>
 <li>
 Perform Investigator Study File reconciliation: request any new or updated site-related essential documents and review them for content, consistency with other documents, and compliance with local regulatory requirements, ICH-GCPs guidelines, SOPs
 </li>
 <li>
 Respond to requests from clinical study sites in a timely fashion
 </li>
 <li>
 Establish and maintain good rapport with clinical study sites
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 At least 2 years of oncology experience as CRA, Coordinator, and/or research nurse.
 </li>
 <li>
 Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health Science &ndash; or its international equivalent
 </li>
 <li>
 Local regulatory requirements knowledge would be a major asset
 </li>
 <li>
 At least one year of experience on an early phase trial
 </li>
 <li>
 Expereince with Breast, Lung, Gastric, and/or Ovarian Tumors would be a major asset
 </li>
 <li>
 Good knowledge of medical terminology and clinical monitoring process
 </li>
 <li>
 Strong ICH-GCPs knowledge
 </li>
 <li>
 Ability to prioritize multiple tasks and achieve project timelines
 </li>
 <li>
 Effective time management in order to meet daily metrics or team objectives
 </li>
 <li>
 Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail
 </li>
 <li>
 Ability to travel up to 60% on average
 
 
 </li>
 </ul>
 
 What TRIO Can Offer You
 
 
 
 <ul>
 <li>
 Competitive Salary
 </li>
 <li>
 3 weeks of vacation plus paid Christmas Closure
 </li>
 <li>
 2 weeks paid personal/sick time
 </li>
 <li>
 100% health benefits for you and your family paid by TRIO
 </li>
 <li>
 Flexible working hours
 </li>
 <li>
 Monthly internet allowance
 </li>
 <li>
 401K Program 5% Salary Contribution
 </li>
 <li>
 Home office allowance
 </li>
 <li>
 Luggage allowance
 
 
 </li>
 </ul>
 Pay Range: $112,000 - $146,000. Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.
</div>

Clinical Research Associate

Flourish Research

<div>Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. 
 
We are actively hiring Clinical Research Coordinators at our Century City site location. This is one of our three oncology research sites in the Greater Los Angeles area. These locations are formerly Valkyrie Clinical Trials - we are proud to welcome Valkyrie Clinical Trials to the Flourish Research network! 
 
The Medical Assistant works closely with physicians and the clinical research team to support patient care and clinical trial activities while ensuring an efficient clinic workflow and exceptional patient experience. This role assists with patient intake, clinical procedures, specimen collection, and documentation in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and clinic protocols. 
 
Shift: Monday-Friday, 8:30 AM - 5 PM (occasional weekends and overnights) 
Location: 2080 Century Pk E Suite 803, Los Angeles, CA 90067 
Compensation: $25.00-$33.00/hr, depending on experience 
Benefits: Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays. 
 
RESPONSIBILITIES<ul><li>
Execute protocol-specified patient visits and clinical procedures, which may include, but not limited to, vital signs, EKG/ECG, phlebotomy, injections, specimen collection, and assisting providers with exams and procedures.</li><li>
Coordinate patient flow and room patients while preparing and maintaining examination and treatment areas.</li><li>
Document patient communication, clinical assessments, and treatments accurately within the EMR.</li><li>
Collect, process, and properly store laboratory specimens according to protocol and clinic procedures.</li><li>
Administer medications and immunizations as directed and supervised by the physician or RN.</li><li>
Assist in scheduling and conducting patient visits while ensuring adherence to protocol timelines and clinic workflows.</li><li>
Maintain inventory and ensure availability of clinical supplies and equipment.</li><li>
Receive, organize, scan, and appropriately file clinical documentation within the EMR.</li><li>
Maintain communication with physicians, clinic leadership, research staff, and other members of the care team.</li><li>
Protect confidentiality per HIPAA and all confidentiality agreements.</li><li>
Maintain a clean, safe, and organized clinical environment.</li><li>
Represent Flourish professionally in all interactions.</li><li>
Additional duties as assigned by management.</li></ul>
QUALIFICATIONS<ul><li>
High school diploma or equivalent required</li><li>
Current Medical Assistant Certification required</li><li>
Current CPR certification required</li><li>
CPT1 preferred</li><li>
Minimum of 1&ndash;2 years of experience providing medical support in a clinical setting</li><li>
Oncology experience preferred</li><li>
Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, injections, and specimen processing</li><li>
Familiar with EMR documentation and clinical workflows</li><li>
Ability to recognize and appropriately respond to emergency situations</li><li>
Impeccable organizational skills and attention to detail</li><li>
Excellent communication and interpersonal skills to effectively interact with physicians, clinical staff, patients, and research teams</li><li>
An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven</li><li>
High-level critical thinking skills</li><li>
Working knowledge of medical terminology and laboratory collection, processing, and storage procedures</li><li>
Proficiency with computers and Microsoft Office Suite</li></ul>
Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others! 
 
Flourish Research is where clinical trials thrive. 
 
Flourish Research is one of the industry&rsquo;s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. 
 
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. 
 
Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. 
 
Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU! 
 
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
4PZAXSmAzD</div>

Medical Assistant - Clinical Research

<div>
 
 
 
 
 Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives!&nbsp;&nbsp;
 
 We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
 
 
 
 We are actively hiring Clinical Research Coordinators at our Century City site location. This is one of our three oncology research sites in the Greater Los Angeles area. These locations are formerly Valkyrie Clinical Trials - we are proud to welcome Valkyrie Clinical Trials to the Flourish Research network!
 
 
 
 The
 
 Medical Assistant
 
 works closely with physicians and the clinical research team to support patient care and clinical trial activities while ensuring an efficient clinic workflow and exceptional patient experience. This role assists with patient intake, clinical procedures, specimen collection, and documentation in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and clinic protocols.
 
 
 
 Shift:&nbsp;
 
 Monday-Friday, 8:30 AM - 5 PM (occasional weekends and overnights)
 
 
 Location:&nbsp;
 
 2080 Century Pk E Suite 803, Los Angeles, CA 90067
 
 
 Compensation:&nbsp;&nbsp;
 
 $25.00-$33.00/hr, depending on experience
 
 
 Benefits:&nbsp;&nbsp;
 
 Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays.
 
 
 
 RESPONSIBILITIES
 
 
 
 
 <ul>
 <li>
 
 
 Execute protocol-specified patient visits and clinical procedures, which may include, but not limited to, vital signs, EKG/ECG, phlebotomy, injections, specimen collection, and assisting providers with exams and procedures.
 
 
 </li>
 <li>
 
 
 Coordinate patient flow and room patients while preparing and maintaining examination and treatment areas.
 
 
 </li>
 <li>
 
 
 Document patient communication, clinical assessments, and treatments accurately within the EMR.
 
 
 </li>
 <li>
 
 
 Collect, process, and properly store laboratory specimens according to protocol and clinic procedures.
 
 
 </li>
 <li>
 
 
 Administer medications and immunizations as directed and supervised by the physician or RN.
 
 
 </li>
 <li>
 
 
 Assist in scheduling and conducting patient visits while ensuring adherence to protocol timelines and clinic workflows.
 
 
 </li>
 <li>
 
 
 Maintain inventory and ensure availability of clinical supplies and equipment.
 
 
 </li>
 <li>
 
 
 Receive, organize, scan, and appropriately file clinical documentation within the EMR.
 
 
 </li>
 <li>
 
 
 Maintain communication with physicians, clinic leadership, research staff, and other members of the care team.
 
 
 </li>
 <li>
 
 
 Protect confidentiality per HIPAA and all confidentiality agreements.
 
 
 </li>
 <li>
 
 
 Maintain a clean, safe, and organized clinical environment.
 
 
 </li>
 <li>
 
 
 Represent Flourish professionally in all interactions.
 
 
 </li>
 <li>
 
 
 Additional duties as assigned by management.
 
 
 </li>
 </ul>
 
 
 
 
 QUALIFICATIONS
 
 
 
 
 <ul>
 <li>
 
 
 High school diploma or equivalent required
 
 
 </li>
 <li>
 
 
 Current Medical Assistant Certification required
 
 
 </li>
 <li>
 
 
 Current CPR certification required
 
 
 </li>
 <li>
 
 
 CPT1 preferred
 
 
 </li>
 <li>
 
 
 Minimum of 1&ndash;2 years of experience providing medical support in a clinical setting
 
 
 </li>
 <li>
 
 
 Oncology experience preferred
 
 
 </li>
 <li>
 
 
 Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, injections, and specimen processing
 
 
 </li>
 <li>
 
 
 Familiar with EMR documentation and clinical workflows
 
 
 </li>
 <li>
 
 
 Ability to recognize and appropriately respond to emergency situations
 
 
 </li>
 <li>
 
 
 Impeccable organizational skills and attention to detail
 
 
 </li>
 <li>
 
 
 Excellent communication and interpersonal skills to effectively interact with physicians, clinical staff, patients, and research teams
 
 
 </li>
 <li>
 
 
 An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
 
 
 </li>
 <li>
 
 
 High-level critical thinking skills
 
 
 </li>
 <li>
 
 
 Working knowledge of medical terminology and laboratory collection, processing, and storage procedures
 
 
 </li>
 <li>
 
 
 Proficiency with computers and Microsoft Office Suite
 
 
 </li>
 </ul>
 
 
 
 Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!
 
 
 
 Flourish Research is where clinical trials thrive.
 
 
 
 Flourish Research is one of the industry&rsquo;s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research.
 
 
 At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality.
 
 
 Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
 
 
 Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
 
 
 
 
 Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.&nbsp;
 
 
 
 
 
</div>

Explore 264+ Assistant clinical research coordinator pediatrics in Los Angeles this March. Find roles across top companies and apply now to boost your career.

264 assistant clinical research coordinator pediatrics jobs In Los Angeles

Assistant Clinical Research Coordinator - Pediatrics

Research Nurse Coordinator (20% Limited)

Clinical Research Coordinator - Pediatrics

Clinical Research Coordinator - Radiological Sciences

Clinical Research Associate

Medical Assistant - Clinical Research

Medical Assistant - Clinical Research