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clinical research coordinator i

research assistant

Getty

<div>
 Getty is committed to creating a welcoming workplace that reflects the various backgrounds of the communities we serve. We value differences in the pursuit of inquiry and knowledge, mutual understanding, respect, trust, transparency, and cooperation. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship or immigration status, color, disability, ethnicity, familial status, gender identity and/or expression, genetic information, marital status, national origin, race, religion, sex, sexual orientation, veteran status, or any other protected status.
 
 
 
 Job Summary
 
 
 
 The Getty Research Institute is seeking a Research Assistant who will work with the associate director of the Research and Knowledge Creation Division, facilitating research and/or assisting with programs, publications, and exhibitions. The ideal candidate will be a graduate student with experience in Art History, Information Studies, or Digital Humanities, with excellent data management skills and diverse research experience. Field of specialization is open. This is a 2-year, limited-term appointment.
 
 
 
 Major Job Responsibilities
 
 
 
 <ul>
 <li>
 Conducts research on various topics related to art history, digital humanities, and the wider field of scholarly communications
 </li>
 <li>
 Gathers, processes, and presents institutional data on current practices and programs in peer academic institutions, as well as galleries, libraries, archives, and museums (GLAM)
 </li>
 <li>
 Proofreads and edits, as needed
 </li>
 <li>
 Assists with the creation of reports, project websites, and PowerPoint presentations
 </li>
 <li>
 May copyedit and review texts for public dissemination or publication
 </li>
 <li>
 Requests images for exhibitions and/or publications; researches and obtains art and image permissions
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in art history or related field; Master&rsquo;s degree or some graduate work preferred
 </li>
 <li>
 0-2 years research experience (education may be considered)
 </li>
 <li>
 Strong skills in gathering, manipulating, analyzing, and presenting qualitative and quantitative data
 
 
 </li>
 </ul>
 Please note: This position is not eligible for employer-based immigration sponsorship. Applicants must have authorization to work for Getty in the United States without the need for sponsorship, currently or in the future.
 
 
 
 Knowledge, Skills And Abilities
 
 
 
 <ul>
 <li>
 Background in Art History (field of specialization is open, but familiarity with art outside of the West is highly desirable), Information Studies, Digital Humanities, or related discipline
 </li>
 <li>
 Attention to detail
 </li>
 <li>
 Strong communication skills
 </li>
 <li>
 Ability to manage multiple projects in a timely manner
 </li>
 <li>
 Ability to build relationships, partner with others and work on teams
 </li>
 <li>
 Ability to set and meet deadlines for oneself
 </li>
 <li>
 Engagement with the broad scholarly landscape of the humanities
 </li>
 <li>
 Proficiency in Microsoft Office (required) and Adobe software suite (preferred)
 </li>
 <li>
 Proficiency with various cloud-based research tools, such as Zotero and Notebook LM, or a willingness to learn these skills
 </li>
 <li>
 Proficiency in data gathering and analysis, including software such as Tableau, experience in wrangling and visualizing data with R or Python, or a willingness to learn these skills
 
 
 </li>
 </ul>
 
 Benefits And Perks
 
 
 
 Here are just some examples that Getty offers/provides for full-time employees:
 
 
 <ul>
 <li>
 Medical, Dental, and Vision insurance coverage, starting on date of hire. Getty pays 75%-95% of the premium, depending on the plan selected.
 </li>
 <li>
 403(b) Employee Investment retirement plan &ndash; with up to 5% Getty Match
 </li>
 <li>
 Getty contribution of 6%, on behalf of employee, to 401(a) retirement account
 </li>
 <li>
 Educational Assistance and professional development
 </li>
 <li>
 Paid Vacation, Sick, and Personal Days
 </li>
 <li>
 12 Paid Holidays
 </li>
 <li>
 Many positions have bi-weekly Off-Fridays
 </li>
 <li>
 On-Site Fitness Center at Getty Center
 </li>
 <li>
 Community service opportunities
 
 
 </li>
 </ul>
 To learn more about our comprehensive benefits and long list of perks, go to
 
 Getty HR
 
 .
</div>

Research Assistant

Alston & Bird

<div>THE FIRM
As a leading international law firm, we are dedicated to excellence through impactful communication, collaboration, and community involvement. Our company culture has earned us one of the &quot;100 Best Companies to Work For&quot; for 26 consecutive years. This honor, along with many others, highlights our commitment to innovation and professional development. At Alston &amp; Bird LLP, our foundation is made of trust, reliability, and compassion.
JOB DESCRIPTION
Responsible for supporting the administration of the Research Services department and with the provision of retrieval research services and access to resources.
ESSENTIAL DUTIES
<ul><li>Pull cases, dockets, court documents, and respond to other ready reference questions as assigned utilizing the most efficient and cost-effective resources
</li><li>Procure document retrieval of journal articles, book chapters/sections, and other legal and non-legal documents per the prescribed departmental process
</li><li>Support large data projects/requests, department initiatives, and other projects as assigned
</li><li>Provide excellent service to attorneys, management, staff, and other professionals.
</li><li>Work consistently and effectively in a team environment.
</li></ul>SKILLS NEEDED TO BE SUCESSFUL
<ul><li>Familiarity with the effective use of retrieval resources, including but not limited to, Westlaw, Lexis, LexMachina, Pacer, CourtLink and others
</li><li>Proficiently utilizes both legal and non-legal research resources as well as internal Firm databases
</li><li>Proficiency in Microsoft Office Suite with strong working knowledge of Outlook, Excel, Word, and PowerPoint
</li><li>Responsiveness and demonstrated ability to manage and prioritize competing deadlines
</li><li>Client service orientation combined with excellent verbal and written communication skills
</li><li>Strong organizational and time management skills with excellent attention to detail
</li><li>Ability to work in a collaborative, service-oriented team, yet also independently with minimal supervision
</li></ul>EDUCATION &amp; EXPERIENCE
<ul><li>College degree required
</li><li>Some library, law firm or research experience preferred
</li></ul>PHYSICAL EFFORT
<ul><li>Repetitive motions substantial movements of the wrists, hands and/or fingers
</li><li>Crouching, kneeling, standing, climbing, stooping, walking, pushing, pulling and lifting
</li><li>Talking expressing or exchanging ideas by means of spoken word
</li><li>Ability to convey detailed or important spoken instructions to other workers accurately
</li><li>Hearing ability to receive detailed information through oral communication
</li><li>Sitting most of the time
</li></ul>LOCATION SPECIFIC INFORMATION
The salary range for this role is $68,000 to $70,000 annually, which is based on a 37.5-hour work week. This range is only applicable for jobs to be performed in Los Angeles . This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee&rsquo;s pay within the salary range will be based on numerous factors including, but not limited to, relevant education, qualifications, experience, skills, and business or organizational needs.
EQUAL OPPORTUNITY EMPLOYER
Alston &amp; Bird LLP is an Equal Opportunity Employer does not discriminate on the bases of any status protected under federal, state, or local law. Applicants will be considered regardless of their sex, race, age, religion, color, national origin, ancestry, physical disability, mental disability, medical condition (associated with cancer, a history of cancer, or genetic characteristics), HIV/AIDS status, genetic information, marital status, sexual orientation, gender, gender identity, gender expression, military and veteran status, or other protected category under the law on the basis of race, color, religion, sex, age, sexual orientation, gender identity and/or expression, national origin, veteran status or disability in relation to our recruiting, hiring, and promoting practices.
The statements contained in this position description are not necessarily all-inclusive, additional duties and responsibilities may be assigned, and requirements may vary from time to time.
Professional business references and a background screening will be required for all final applicants selected for a position.
If you need assistance or an accommodation due to a disability you may contact donavan.mclean@alston.com .
Alston &amp; Bird is not currently accepting resumes from agencies for this position. If you are a recruiter, search firm, or employment agency, you will not be compensated in any way for your referral of a candidate even if Alston &amp; Bird hires the candidate.</div>

Headlands Research

<div><div>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.</div> 


 Rolling Hills Estates, CA 
 Peninsula Research Associates 
 Full-Time | Mon&ndash;Fri, 8:00am&ndash;5:00pm)
<h3 class="jobSectionHeader">
Looking for more than just high-volume blood draws?</h3>

If you're an experienced phlebotomist or lab technician who takes pride in precision, patient care, and doing things the right way&mdash;not just the fast way&mdash;clinical research may be the next step in your career.

At Peninsula Research Associates, our lab professionals work in a structured, calm, and purpose-driven environment, supporting clinical trials that help advance new treatments for allergy and immunology-related conditions. 


<h2 class="jobSectionHeader">Why Lab Professionals Choose Clinical Research</h2>
<ul>
<li>Predictable weekday schedule (no nights, no weekends, no emergency draws)
</li>
<li>More time and control during patient visits and specimen handling
</li>
<li>Specialized lab work beyond routine phlebotomy (processing, PK handling, shipping)
</li>
<li>Smaller, collaborative teams where your role is respected
</li>
<li>Meaningful purpose&mdash;your work directly supports future medical treatments
</li>
<li>Clear growth pathway into higher-paying clinical research roles
</li>
</ul>This role is ideal for lab professionals who value accuracy, organization, and consistency, and who want to grow their skills beyond traditional lab or hospital settings. 


<h2 class="jobSectionHeader">Career Growth Opportunity</h2>

PRA strongly supports internal growth. High-performing Laboratory Technicians / Phlebotomists have the opportunity to progress into a Clinical Research Coordinator (CRC) role, which offers:
<ul>
<li>Increased responsibility
</li>
<li>Broader study ownership
</li>
<li>Higher compensation
</li>
<li>Long-term career growth within clinical research
</li>
</ul>If you're curious about research and want a role that can evolve with you, this position offers a clear entry point. 


<h2 class="jobSectionHeader">Position Details</h2>
<ul>
<li>Position Type: Full-time
</li>
<li>Schedule: Monday&ndash;Friday, 8:00am&ndash;5:00pm
</li>
<li>Location: Onsite in Rolling Hills Estates, CA (no remote or hybrid)</li></ul> 

<h2 class="jobSectionHeader">The Role</h2>

The Laboratory Technician / Phlebotomist is a key member of the clinical research team, supporting studies through specimen collection, processing, documentation, and shipment in compliance with Good Clinical Practice (GCP), study protocols, and safety regulations.

You'll work in a controlled clinical research environment with scheduled visits, detailed protocols, and strong operational support, allowing you to focus on quality and precision. 


<h2 class="jobSectionHeader">Who Thrives in This Role</h2>
<ul>
<li>Lab professionals who value precision over speed
</li>
<li>Phlebotomists looking for predictability and balance
</li>
<li>Candidates curious about clinical research and career growth
</li>
<li>Team players who take pride in quality, compliance, and patient experience
</li>
</ul>Responsibilities:
<ul>
<li>Laboratory and Clinical Procedures
<ul><li>Perform phlebotomy, urine collection, and sample processing (centrifuging, aliquoting, labeling).</li>
<li>Prepare lab kits for each subject based on study protocols.</li>
<li>Ship biological specimens following IATA guidelines and protocol requirements.</li>
<li>Maintain specimen logs, shipping records, temperature logs, and other documentation.</li>
<li>Conduct point-of-care tests (e.g., urine drug screens, pregnancy tests).</li>
<li>Assist with patient procedures including vital signs, ECGs, and physical/neurological exam setups.</li>
<li>Clean and sanitize lab equipment and work areas daily.</li>
<li>Perform and document equipment calibration and ensure safety compliance (OSHA, HIPAA).</li>
</ul></li><li>Data and Documentation
<ul><li>Accurately record lab results and maintain electronic and paper logs in systems such as CRIO or eCRFs.</li>
<li>Respond to and resolve electronic data queries.</li>
<li>Verify accuracy and completeness of data entries and study documentation.</li>
<li>Participate in quality control and assurance initiatives to ensure regulatory compliance.</li>
</ul></li><li>Operational Support
<ul><li>Monitor and maintain inventory of lab kits and supplies.</li>
<li>Order dry ice and other lab necessities.</li>
<li>Destroy expired kits and log per protocol.</li>
<li>Support preparation of study-specific training materials and lab manuals.</li>
<li>Collaborate with study coordinators and medical staff to meet visit protocol requirements.</li>
<li>May assist with infusion monitoring under clinician supervision.</li>
</ul>
</li></ul>Requirements:
<ul>
<li>Must be certified in phlebotomy</li>
<li>Must have at least one full year of experience performing phlebotomy multiple times daily</li>
<li>Previous experience in clinical research is a huge plus</li>
<li>Proficient with Microsoft Office (Excel, Outlook, Word) and database systems.</li>
<li>Must be comfortable with performing Research Assistant tasks</li>
<li>Ability to handle potentially hazardous materials safely.</li>
<li>Strong organizational, time management, and multitasking skills.</li>
<li>Excellent verbal and written communication; strong interpersonal skills.</li>
<li>Ability to work independently and as part of a cross-functional team.</li>
<li>Customer-service mindset and high level of professionalism.</li></ul></div>

Laboratory Technician/Phlebotomist

Cedars-Sinai

<div>
 
 Job Description
 
 
 
 The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
 
 
 
 Join our team and use your skill with an organization known nationally for excellence in research!
 
 
 
 
 Job Summary:
 
 
 
 The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.
 
 
 
 Job Duties and Responsibilities:
 
 
 
 Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
 
 
 Evaluates and abstracts clinical research data from source documents.
 
 
 Ensures compliance with protocol and overall clinical research objectives.
 
 
 Completes Case Report Forms (CRFs).
 
 
 Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
 
 
 Provides supervised patient contact or patient contact for long term follow-up patients only.
 
 
 Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
 
 
 Assists with clinical trial budgets and patient research billing as needed
 
 
 Schedules patients for research visits and research procedures.
 
 
 Responsible for sample preparation and shipping and maintenance of study supplies and kits.
 
 
 Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
 
 
 Maintains research practices using Good Clinical Practice (GCP) guidelines.
 
 
 Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
 
 
 Participates in required training and education programs.
 
 
 
 Qualifications
 
 
 
 
 Education:
 
 
 
 High School diploma/GED required.
 
 
 BA/BS degree in Science, Sociology or related degree preferred.
 
 
 
 Experience:
 
 
 
 Understanding of general research objectives.
 
 
 
 1 Year Of Clinical Research Related Experience Preferred.
 
 
 
 <ul>
 <li>
 Excellent language skills and understanding of Grants, Manuscript, and Abstract guidelines.
 </li>
 <li>
 Strong verbal and writing ability as well as communication, computer, organization, personnel and time-management skills.
 </li>
 <li>
 Proficiency in Word, PowerPoint and Excel.
 </li>
 <li>
 Ability to work independently, set priorities, and handle multiple tasks requiring attention to detail.
 </li>
 <li>
 Previous experience in research environment preferred.
 
 
 </li>
 </ul>
 Physical Demands:
 
 
 <ul>
 <li>
 Able to perform moderate lifting.
 </li>
 <li>
 Able to sit, stand and walk for prolonged periods of time
 </li>
 <li>
 Able to read papers and online documents.
 </li>
 <li>
 Able to operate standard office equipment
 </li>
 <li>
 Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions.
 </li>
 </ul>
</div>

Heart Institute Clinical Research Associate I - per diem/ Cheng Lab

Children's Hospital Los Angeles (CHLA)

<div>
 
 Schedule:
 
 Monday-Friday, 8:00 AM-5:00 PM
 
 
 
 Purpose Statement/Position Summary:
 
 The Clinical Research Office team is responsible for recruiting, enrolling, and coordinating clinical research studies for the Heart Institute. 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. Additional responsibilities include regulatory work, study coordination, patient interaction, and sometimes facilitating contracts and budgets.
 
 
 
 Minimum Qualifications/Work Experience:
 
 1+ year experience in clinical trial coordination or computerized databases.
 
 
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 Contracts, budget, and invoicing experience.
 </li>
 <li>
 Regulatory experience.
 
 
 </li>
 </ul>
 
 Education/Licensure/Certifications:
 
 High School Diploma, GED, or equivalent required. Bachelor&rsquo;s degree preferred in related scientific field preferred. Certified clinical research associate/coordinator preferred.
</div>

Clinical Research Coordinator I

UCLA Health

<div><div>Description
UCLA is part of a large consortium funded by NIH to better understand brain and cognitive development from childhood to early adulthood (ABCD Study). Project involves neuroimaging and various behavioral assessments. The Staff Research Associate will assist in all aspects related to data acquisition and daily lab operations.
Responsibilities include but are not limited to:<ul><li>
Conduct day-to-day activities related to the ABCD projects.
</li><li>Work closely with other members of the research team and PIs at UCLA and the other participating sites to co-ordinate study visits and compliance with study protocols</li><li>
Coordinate with center administrators to place supply orders</li><li>
Assist investigators in the preparation of figures, posters and papers</li><li>
Other clerical activities</li><li>
Assist with all aspects of data acquisition for the center projects</li><li>
Ensure proper behavioral data acquisition via REDCap</li><li>
Conduct MRI scanning together with other members of the research team, operate MRI scanning and collecting data</li><li>
Perform initial QC to ensure viability of collected data
</li><li>Transfer data according to study protocols</li><li>
Maintain study records</li></ul>
Hourly Salary Range: $28.69 &ndash; 34.21</div><div>
Qualifications
Required:<ul><li>
Ability to perform tasks in an efficient, well-organized and timely manner with frequent changes in priorities and deadlines.</li><li>
Skill in setting priorities, follow through on assigned tasks and adhering to procedures and deadlines.</li><li>
Ability to work collaboratively in a team.</li><li>
Ability to work independently with minimal supervision.</li><li>
Ability to assess situations and problem solve using own judgment.</li><li>
Computer skills including word processing, email systems, spreadsheets, including the ability to enter data and maintain study records.</li><li>
Ability to communicate clearly, verbally and in writing, with staff, researchers, and research subjects at different cultural and educational levels.</li><li>
Experience working with pediatric populations
</li></ul>Preferred:<ul><li>
Bachelor&rsquo;s degree in Psychology or Neuroscience
</li><li>Some experience in neuroimaging tools such as FSL, SPM, AFNI, or Freesurfer
</li><li>Ability to work weekends and late evenings.</li></ul></div></div>

Staff Research Associate I

<div><div>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.</div> 


 Rolling Hills Estates, CA 
 Peninsula Research Associates (a Headlands Research site) 
 Full-Time Temporary (3 months with potential to turn into permanent role) | Monday through Friday | Onsite (no opportunities for hybrid or remote)
<h3 class="jobSectionHeader">
For experienced CRCs looking for stability, collaboration, and meaningful work</h3>

If you're an experienced Clinical Research Coordinator I, II, or III who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work&ndash;life balance, Peninsula Research Associates may be the right next step in your career.

Our Rolling Hills Estates site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research&mdash;particularly in vaccines, immunology and allergy studies. 


<h2 class="jobSectionHeader">About Peninsula Research Associates</h2>

Peninsula Research Associates (PRA) is dedicated to advancing medical treatments through the use of innovative techniques and increasing awareness. PRA has achieved significant study results in allergy, asthma, vaccines, otitis media and sinusitis treatment and has earned a reputation for conducting quality research. 


<h2 class="jobSectionHeader">Why Experienced CRCs Choose PRA</h2>
<ul><li>Multi-disciplinary collaboration with seasoned investigators and clinical staff</li>
<li>Strong operational support and clear SOPs</li>
<li>Exposure to complex, meaningful studies&mdash;not just high-volume turnover</li>
<li>A site with long-standing credibility and research maturity</li>
<li>Backing of a growing research network with resources and stability</li>
</ul>
This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision. 


<h2 class="jobSectionHeader">What You'll Do</h2>
<ul><li>Coordinate all aspects of assigned clinical trials from site initiation through close-out</li>
<li>Conduct subject visits and ensure accurate, timely documentation in compliance with ALCOA-C standards</li>
<li>Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs</li>
<li>Manage subject recruitment, informed consent, and retention activities</li>
<li>Ensure timely EDC data entry and resolution of queries</li>
<li>Report and follow up on AEs, SAEs, and protocol deviations</li>
<li>Collaborate with investigators, sponsors/CROs, labs, and internal teams</li>
<li>Prepare for and participate in monitoring visits, audits, and inspections</li>
<li>Maintain regulatory documentation and ensure training compliance for amendments and systems</li>
<li>Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)</li>
<li>Attend investigator meetings and provide cross-functional support as needed</li>
<li>Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory</li></ul> 


<h2 class="jobSectionHeader">What We're Looking For</h2>
<ul><li>High school diploma or GED required; Bachelor's degree preferred</li>
<li>At least one year of experience coordinating Phase 2&ndash;4 industry-sponsored clinical trials</li>
<li>Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations</li>
<li>Experience with EDC, IVRS, and clinical research platforms</li>
<li>Proficiency in medical terminology and clinical documentation</li>
<li>Strong organizational skills with the ability to manage multiple studies</li>
<li>Clear, professional verbal and written communication skills</li>
<li>Comfortable working onsite in a collaborative, clinical environment</li></ul> 


<h2 class="jobSectionHeader">Who Thrives in This Role</h2>
<ul><li>CRCs who want structure, support, and accountability</li>
<li>Professionals who value teamwork over silos</li>
<li>Coordinators who care about data quality, patient experience, and compliance</li>
<li>Those ready to grow within a stable, well-established research site</li></ul> 


 Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.</div>

Temporary Clinical Research Coordinator I, II, or III

Explore 208+ Research assistant in Los Angeles this April. Find roles across top companies and apply now to boost your career.

208 research assistant jobs In Los Angeles

Research Assistant

Research Assistant

Laboratory Technician/Phlebotomist

Heart Institute Clinical Research Associate I - per diem/ Cheng Lab

Clinical Research Coordinator I

Staff Research Associate I

Temporary Clinical Research Coordinator I, II, or III