clinical research coordinator - pediatrics

research assistant

clinical research coordinator Jobs in Los Angeles

clinical research coordinator

case manager i - prcs Jobs in Los Angeles

case manager i - prcs

clinical research associate Jobs in Los Angeles

clinical research associate

clinical research coordinator - pediatrics Jobs in Los Angeles

clinical research coordinator radiological sciences

UCLA Health

<div><div><b>Description</b><p></p><p>
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.
</p>
<p>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.
</p>
<p>Salary: $36.37 - $58.52 hourly<br>
</p><br>
</div><div><b>Qualifications</b><p></p><p>
Required:</p><ul><li>
Bachelors Degree or equivalent experience/training<br>
</li><li>
Minimum 3 years of related experience or training<br>
</li><li>
Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.<br>
</li><li>
Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.<br>
</li><li>
Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.<br>
</li><li>
Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.<br>
</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.<br>
</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.<br>
</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

<div><div><b>Description</b><p></p><p>
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.
</p>
<p>Within the UCLA Brain Tumor Imaging Laboratory (BTIL) in the Department of Radiological Sciences, the Research Associate plays a key role in advancing preclinical imaging research focused on brain tumor biology. This position supports the lab&rsquo;s scientific mission by performing molecular biology experiments, maintaining cell cultures, and conducting mouse xenograft studies. The role offers the opportunity to contribute directly to innovative cancer research in a dynamic, collaborative laboratory environment.
</p>
<p>Salary: $31.21 - $50.21 hourly<br>
</p><br>
</div><div><b>Qualifications</b><p></p><p>
Required:</p><ul><li>
BA/BS and/or equivalent combination of education and experience/training.<br>
</li><li>
1 year of demonstrated knowledge of basic genetics, molecular biology and biochemical principles.<br>
</li><li>
1 year of familiarity with basic laboratory equipment, including centrifuge, pH meter, incubators, biosafety cabinet hoods, PCR machines and electrophoresis apparatus.<br>
</li><li>
Strong interpersonal skills for interaction to communicate diplomatically and effectively with faculty, patients, physicians, collaborators, researchers, and other University staff.<br>
</li><li>
Ability to learn new methods and protocols and to adapt these to current laboratory situations<br>
</li><li>
Experience with working with mice, including survival surgeries (e.g. intracranial implantation) and drug administration (intraperitoneal, intravenous, and oral gavage)</li></ul><br>
<p>
Preferred:
</p><ul><li>
Strong molecular biology skill-set, including experience with cell culture, PCR, RT-PCR, Western blot, and cloning.</li></ul></div></div>

Staff Research Associate II - Radiological Sciences

<div><div><b>Description</b><p></p><p>
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.</p><p>
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.</p><p>
*This is a limited role which may convert to career.*</p><p>
Hourly range: $70.59-$106.80</p></div><div><b>
Qualifications</b><p></p>
<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><b>Description</b><p></p>
<p>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.</p><p>
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.</p><p>
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.</p><p><i>
This is a limited position that may convert to career.</i></p><p></p><p>
Salary Range: $36.37 - $58.52 Hourly</p>
</div><div><b>Qualifications</b><p></p><p><b>
Required:</b></p><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><p></p><p><b>
Preferred:</b></p><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

ICON plc

<div></div><div><div>What You Will Be Doing:</div><div></div><ul><li>
Serve as the primary point of contact between investigational sites and the sponsor</li><li>
Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out</li><li>
Ensure site compliance with ICH-GCP, SOPs, and regulations</li><li>
Maintain up-to-date documentation in CTMS and eTMF systems</li><li>
Support and track site staff training and maintain compliance records</li><li>
Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting</li><li>
Support subject recruitment and retention efforts at the site level</li><li>
Oversee drug accountability and ensure proper storage, return, or destruction</li><li>
Resolve data queries and drive timely, high-quality data entry</li><li>
Document site progress and escalate risks or issues to the clinical team</li><li>
Assist in tracking site budgets and ensuring timely site payments (as applicable)</li><li>
Collaborate with cross-functional partners including CTAs, LTMs, and CTMs</li></ul><div></div><div>
You are:</div><ul><li>
A graduate with a Bachelor&rsquo;s degree in Life Sciences or equivalent, or a qualified RN</li><li>
Eligible to work in United States without visa sponsorship</li><li>
A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry</li><li>
Experienced monitoring Oncology Hematology clinical trials</li><li>
Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF</li><li>
A clear communicator, problem-solver, and collaborative team player</li><li>
Willing and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Los Angeles, CA near major HUB airports to support efficient regional travel</li></ul></div><div></div>

Clinical Research Associate

Flourish Research

<div><p><b>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! </b>We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.<br>
<br>
<b>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!</b><br>
<br>
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols <b>while providing an impeccable patient experience in every, single interaction.</b><br>
<br>
<b>Shift: </b>Monday-Friday, 8:30 AM - 5 PM (occasional weekends and overnights)<br>
<b>Location: </b>2080 Century Pk E Suite 803, Los Angeles, CA 90067<br>
<b>Compensation: </b>$31.00-$43.00/hr depending on experience<br>
<b>Benefits: </b>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.<br>
<br>
<b>RESPONSIBILITIES</b></p><ul><li>
Execute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.</li><li>
Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs.</li><li>
Obtain informed consent per federal regs, GCP, and IRB requirements.</li><li>
Ethically recruit qualified subjects to meet enrollment timelines.</li><li>
Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies.</li><li>
Schedule and conduct visits per protocol timelines.</li><li>
Protect confidentiality per HIPAA and all confidentiality agreements.</li><li>
Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor.</li><li>
Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).</li><li>
Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy.</li><li>
Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies.</li><li>
Represent Flourish professionally in all interactions.</li><li>
Additional duties as assigned by management.</li></ul><div><b>
QUALIFICATIONS</b><ul><li>
Bachelor's degree preferred, but not required</li><li>
Must have oncology clinical research experience</li><li>
Minimum of two years of clinical research experience</li><li>
Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injections</li><li>
Familiar with e-source reporting via an electronic platform</li><li>
A clear understanding of ICH, FDA, and GCP regulations</li><li>
Impeccable organizational skills and attention to detail</li><li>
Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources</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 lab collection/processing/storage procedures</li><li>
Proficiency with computers and Microsoft Office Suite</li></ul></div><p>
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!<br>
<br>
<b>Flourish Research is where clinical trials thrive.</b><br>
<br>
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.<br>
<br>
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.<br>
<br>
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.<br>
<br>
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!<br>
<br>
<b><i>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.</i></b></p><p>
</p><p>99oVBP6ill</p></div>

Clinical Research Coordinator

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
Standard (Mon-Fri)<p></p><p><b>
Environmental Conditions</b></p>
Fluctuating Temps hot/cold<p></p><p><b>
Job Description</b></p><p></p>
Join Us as a Senior Clinical Research Associate (Level I) &ndash; Make an Impact at the Forefront of Innovation<br>
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
<br>
<br>
As part of our global team, you&rsquo;ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.<br>
<br>
What You&rsquo;ll Do:<br>
<ul><li>Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable</li><li>Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.</li><li>Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.</li><li>Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.</li><li>Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).</li><li>Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.</li><li>Responds to company, client and applicable regulatory requirements/audits/inspections.</li><li>Maintains &amp; completes administrative tasks such as expense reports and timesheets in a timely manner.</li><li>Contributes to other project work and initiatives for process improvement, as required.</li></ul><br>
Education and Experience Requirements:
<br>
<ul><li>Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
</li><li>Valid driver's license where applicable</li><li>In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
</li></ul><br>
Knowledge, Skills and Abilities:
<br>
<ul><li>Effective clinical monitoring skills</li><li>Demonstrated understanding of medical/therapeutic area knowledge and medical terminology</li><li>Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents</li><li>Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving</li><li>Ability to manages Risk Based Monitoring concepts and processes</li><li>Effective oral and written communication skills, with the ability to communicate effectively with medical personnel</li><li>Ability to maintain customer focus through the utilization of good listening skills, attention to detailand the ability to perceive customers&rsquo; underlying issues</li><li>Effective interpersonal skills</li><li>Strong attention to detail</li><li>Effective organizational and time management skills</li><li>Ability to remain flexible and adaptable in a wide range of scenarios</li><li>Ability to work in a team or independently as required</li><li>Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software</li><li>Good English language and grammar skills</li><li>Good presentation skills</li></ul><br>
Working Conditions and Environment:
<br>
<ul><li>Working Conditions and Environment:</li><li>Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.</li><li>Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.</li><li>May also include extended overnight stays.</li><li>Exposure to biological fluids with potential exposure to infectious organisms.</li><li>Personal protective equipment required such as protective eyewear, garments and gloves.</li><li>Exposure to fluctuating and/or extreme temperatures on rare occasions.</li><li>Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.</li></ul></div><p></p>

Senior CRA

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