clinical research assistant

assistant clinical research coordinator Jobs in Los Angeles

assistant clinical research coordinator

assistant clinical research coordinator - pediatrics Jobs in Los Angeles

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assistant research adminstrator

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clinical care coordinator

clinical research coordinator

Amicis Research Center

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   SALARY RANGE : $25-$45/HR DEPENDING ON EXPERIENCE
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    ONLY FOR THOSE CURRENTLY LIVING IN LOS ANGELES COUNTY OR CAN COMMUTE TO OUR CLINIC IN LOS ANGELES COUNTY
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   Company Description
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  Amicis Research Center is dedicated to excellence in clinical research, guided by the principles of enthusiasm, motivation, and empathy. The organization prioritizes fulfilling research protocol requirements with dedication and fosters a culture of transparency and trust with its research participants. Supported by a skilled team of research assistants, coordinators, nurses, and physicians, Amicis Research Center emphasizes participant well-being while contributing to meaningful advancements in healthcare. Located in Los Angeles, CA, the center collaborates with CROs and sponsors to drive healthcare innovation.
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   Role Description
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  This is a full-time, on-site role for a Clinical Research Coordinator based in Los Angeles, CA. 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. Additional responsibilities include coordinating with researchers, study participants, and stakeholders to organize, execute, and monitor clinical trials effectively.
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   Qualifications
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   Proficiency in managing and obtaining Informed Consent and ensuring ethical compliance in conducting studies
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   Knowledge and experience with research protocols and clinical procedures
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   Hands-on Clinical Research Experience working with clinical data and participants
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   Experience in planning and conducting Clinical Trials
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   Strong organizational and communication skills
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   Proficiency in maintaining accurate and detailed documentation
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   Ability to work collaboratively with a multidisciplinary team
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   Bachelor's degree in a related field or equivalent professional experience in clinical research
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   Certification in Clinical Research Coordination (e.g., ACRP, SOCRA) is a plus
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Clinical Research Coordinator

Howard L Sofen M.D. A Medical Corporation

<p>We are looking for a responsible, detail-oriented and hard-working individual to work as a clinical research coordinator at our office specializing in dermatology research. It is a fast-paced working environment with a high volume of trials being conducted for a variety of dermatological skin conditions. The ideal candidate would have a science background (although not required), have high attention to detail, enjoy working with patients and have a passion for research. Clinical research coordinators will oversee all administrative aspects of the research study and work alongside our other dedicated medical staff members to execute each research study in accordance with the respective protocol.</p><p>Our company has a long-standing track record of former employees who have gone on to various professional schools including medical school, dental school and physician assistant graduate programs. This job offers candidates interested in pursuing advanced degrees a unique and beneficial opportunity to gain valuable clinical experience as well as one-on-one face time with patients.</p><p>Qualifications should include:</p><p>Detail-oriented, organized, responsible self-motivated, works well with others, has a passion for research, has a science background (although not required), and Spanish speaking is a plus</p><p>Job Type: Full-time</p><p>Pay: $26.00 - $30.00 per hour</p><p>Benefits:</p><ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Work Location: In person</p>

o2 technologies inc

<p><b>Overview</b><br/>Join our dynamic clinical research team as a Clinical Research Coordinator (Regulatory), where your expertise will drive the success of groundbreaking clinical trials. This vital role involves managing regulatory documentation, ensuring compliance with industry standards, and supporting the integrity of research processes.</p><p>Skills:</p><p>3+ years of experience in clinical research supporting regulatory compliance and study documentation.</p><p>Skilled in managing and tracking regulatory documents including IRB correspondence, FDA forms, CVs, medical licenses, and SAE submissions.</p><p>Strong knowledge of FDA GCP, GLP, and local IRB regulatory requirements</p><p>1+ year oncology clinical research experience</p><p>CCRP certification with working experience in Epic systems</p><p>Job Type: Temporary</p><p>Pay: $67.00 per hour</p><p>Expected hours: 40 per week</p><p>Work Location: In person</p>

Clinical Research Coordinator(Regulatory)

UCLA Health

<div><div><b>Description</b><p></p><p>
The Department of Medicine, Division of Gastroenterology is seeking to hire an Assistant Clinical Research Coordinator to support the successful execution of clinical research studies and trials. In this role, you will work closely with the Clinical Research Coordinator and Senior Clinical Research Coordinator to keep studies running smoothly, on schedule, and in full compliance with protocols and regulations.</p><p>
You will assist with day‑to‑day study operations, help organize and prioritize project tasks, and ensure key activities are completed accurately and on time. Your work will directly support study planning, regulatory adherence, and overall trial management&mdash;making you an essential part of the research team.</p><p>
This position is ideal for someone detail‑oriented, proactive, and eager to grow in clinical research while contributing to studies that advance patient care and medical knowledge.</p><p>
Hourly range: $29.28-$47.10</p></div><div><b>
Qualifications</b><p></p><p>
Required:</p><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><p>
Preferred:</p><div><ul><li>
Experience in a Health Care Setting</li></ul></div></div></div>

Assistant Clinical Research Coordinator

Children's Hospital Los Angeles

<div>Location/Org Data : Introduction:
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Join a team that's shaping the future of pediatric care. Children&rsquo;s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services. Here, world-class experts in medicine, research, and education work together to deliver family-centered care to more than 155,000 patients each year. At CHLA, your work will help build brighter tomorrows for the children and families we serve.</div>
Overview:
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Schedule:</b> Monday-Friday, Day Shift</div><div></div><div><b><br>
Purpose Statement/Position Summary:</b> The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects.<br>
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<b>Minimum Qualifications/Work Experience:</b> 1+ years of experience in clinical trial coordination or computerized databases. 1 year of clinical research (study coordination, data management) or related experience preferred. Contracts, budgets, invoicing, and regulatory experience preferred.<br>
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<b>Education/Licensure/Certifications:</b> High School Diploma, GED, or equivalent required. Bachelor's degree in related scientific field preferred. Certified clinical research associate/coordinator preferred.</div>
Pay Scale Information: CHLA values the contribution each Team Member brings to our organization. Final determination of a successful candidate&rsquo;s starting pay will vary based on a number of factors, including, but not limited to, education and experience within the job or the industry. The pay scale listed for this position is generally for candidates who meet the specified qualifications and requirements listed on this specific job description. Additional pay may be determined for those candidates who exceed these specified qualifications and requirements. We provide a competitive compensation package that recognizes your experience, credentials, and education alongside a robust benefits program to meet your needs. Posting Range: $61,152.00-$100,464.00 Location/Org Data : Closing:
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CHLA is a leader in pediatric and adolescent health, in our community, across the nation, and around the world . As a premier Magnet&reg;-recognized teaching hospital, CHLA offers an environment rooted in learning, collaboration, and compassionate care. . We are home to groundbreaking research, clinical innovation, and a culture that supports personal and professional growth.</div><div>
Since 1932, CHLA has been affiliated with the Keck School of Medicine of the University of Southern California. Through this partnership and our own enduring mission, we remain committed to creating hope and building healthier futures.</div></div>

Clinical Research Coordinator I

<div><div><b>Description</b><p></p><p>
The Assistant Clinical Research Coordinator will be part of a centralized clinical research team that conducts clinical trials and registries across multiple pediatric sub-specialties. Under the direction of the Clinical Research Supervisor, this position will assist team members with tasks such as data entry, query resolution, document management, and specimen handling. They will support the team in planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations. The Assistant CRC must be able to adapt to changing priorities and work flexible hours to accommodate 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: $29.28 - $47.10 Hourly</p><br>
</div><div><b>Qualifications</b><p></p><p><b>
Required:</b></p><ul>
</ul><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><p>
</p><p><b>Preferred:</b></p><ul>
<li>Experience in a Health Care Setting.</li></ul></div></div>

Assistant Clinical Research Coordinator - Pediatrics

Headlands Research

<div><div><p>At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.</p></div><p>
 <b>Rolling Hills Estates, CA</b><br>
 <b>Peninsula Research Associates</b><br>
 <b>Full-Time | Monday through Friday | 8:00am - 5:00pm</b></p><h3 class="jobSectionHeader"><b><br>
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<h3 class="jobSectionHeader"><b>Launch Your Career in Healthcare &amp; Research</b></h3><br>
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Are you a recent graduate looking to gain hands-on experience in healthcare or clinical research? This is an exciting opportunity to work directly with patients, support clinical trials, and build real-world skills alongside experienced research professionals.</p>
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As a <b>Clinical Research Assistant</b>, you'll play a key role in supporting study visits, interacting with patients, and ensuring research is conducted safely and accurately. Whether you're planning a future as a Clinical Research Coordinator, healthcare provider, or pursuing advanced education, this role provides a strong foundation and meaningful exposure to a fast-paced, patient-centered environment.</p><br>
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<h3 class="jobSectionHeader"><b>What You'll Do</b></h3>
<ul><li>Study Preparation
<ul><li>Prepare and maintain study documents, including source charts, study binders, regulatory binders, and laboratory kits.</li>
<li>Schedule and confirm subject appointments, including ancillary visits such as diagnostic imaging and vendor-related services.</li>
<li>Understand study protocols, inclusion/exclusion criteria, and regulatory requirements, ensuring compliance with FDA, Sponsor, and Good Clinical Practice (GCP) guidelines.</li>
<li>Assist in participant recruitment by prescreening electronic medical records, following up on referrals, and coordinating outreach efforts.</li>
</ul></li><li>Participant Care and Interaction
<ul><li>Provide subject care, including explaining study procedures, answering questions, and monitoring diary compliance.</li>
<li>Conduct study procedures, such as collecting vital signs, performing ECGs, and completing study questionnaires.</li>
<li>Perform follow-up and reminder calls to ensure subject adherence to visits and study protocols.</li>
<li>Assist with participant stipend tracking and processing.</li>
</ul></li><li>Laboratory and Specimen Handling
<ul><li>Perform blood draws (phlebotomy) and process biological samples, including shipping per study requirements.</li>
<li>Maintain laboratory equipment, supplies, and temperature control systems, ensuring compliance with study protocols.</li>
<li>Generate and file weekly temperature reports for laboratory systems.</li>
</ul></li><li>Data Entry and Management
<ul><li>Enter and verify study data in Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), and other databases.</li>
<li>Address system-generated queries and perform quality control checks to ensure data accuracy and completeness.</li>
<li>Assist with case report forms (CRFs) and source document completion, including query resolution under study coordinator guidance.</li>
</ul></li><li>Administrative and General Support
<ul><li>Maintain and organize participant charts, Investigator Site Files, and other regulatory documents.</li>
<li>Support clinical research coordinators (CRCs) by filing, scanning, and faxing required documents.</li>
<li>Clean, stock, and maintain exam rooms and department supplies to ensure readiness for participant visits.</li>
<li>Participate in investigator meetings, study teleconferences, and trainings.</li>
<li>Assist with onsite or remote clinical research monitor visits.</li></ul></li><br>
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<p></p><h3 class="jobSectionHeader"><b>What Makes You a Great Fit</b></h3>
<ul><li>Strong attention to detail and ability to follow step-by-step procedures</li>
<li>Ability to work efficiently in a fast-paced environment with changing priorities</li>
<li>Strong communication skills and a professional, patient-focused demeanor</li>
<li>Comfortable interacting with a diverse patient population</li>
<li>Proactive, dependable, and eager to learn new skills</li>
<li>Ability to balance multiple tasks and priorities throughout the day</li>
<li>Professional, reliable, and eager to learn</li></ul><br>
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<h3 class="jobSectionHeader"><b>Requirements</b></h3>
<ul><li>Bachelor's degree OR 2 years of college in a health-related program OR completion of a medical assistant, phlebotomist, or other healthcare-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required</li>
<li>CNAs, Medical Assistants, Phlebotomists, and other patient-care healthcare roles heavily preferred</li>
<li>Experience with medical terminology and laboratory procedures preferred.</li>
<li>Strong attention to detail, with the ability to collect, compile, and analyze patient data accurately.</li>
<li>Excellent interpersonal, communication (verbal and written), and customer service skills.</li>
<li>Easily able to learn new computer or website applications (i.e. Electronic Medical Records, Clinial Trial Management Systems, etc.)</li>
<li>Proven ability to prioritize tasks, meet deadlines, and adapt to a fast-paced work environment.</li>
<li>Problem-solving skills with a proactive and solution-oriented approach.</li>
<li>Strong organizational skills with the proven ability to prioritize tasks and meet strict deadlines</li>
<li>Phlebotomy training and experience heavily preferred; willingness to become fully trained required</li></ul><br>
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<h3 class="jobSectionHeader"><b>Why This Role is a Great First Step</b></h3><br>
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<ul>
<li>Gain hands-on experience working directly with patients in a clinical setting</li>
<li>Learn the fundamentals of clinical research and how trials are conducted</li>
<li>Build transferable skills for careers in healthcare, research, or biotechnology</li>
<li>Work alongside experienced professionals who provide training and mentorship</li>
<li>Create a strong foundation for advancement into roles like Clinical Research Coordinator or beyond</li>
<li>Make a meaningful impact by helping bring new treatments and therapies to patients</li></ul><br>
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<p>If you're looking to turn your academic experience into a meaningful, patient-focused career, this is a powerful place to start.</p><p></p><div><div><div><br>
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<p></p><div><div><div><div><div><div><div><div><div><p><i>Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.</i></p>
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</div></div></div></div></div><p><i>Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.</i></p>
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</div></div></div></div></div><div><div><h3 class="jobSectionHeader"><b>Need Assistance?</b></h3>
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<div><div><div><p><i>Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact </i><i>recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.</i></p></div></div></div></div></div></div></div></div><p></p>

Patient-facing Research Assistant

Explore 158+ Clinical research coordinator in Los Angeles this May. Find roles across top companies and apply now to boost your career.

158 clinical research coordinator jobs In Los Angeles

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator(Regulatory)

Assistant Clinical Research Coordinator

Clinical Research Coordinator I

Assistant Clinical Research Coordinator - Pediatrics

Patient-facing Research Assistant