clinical research associate Jobs in Los Angeles

clinical research associate

research assistant

clinical research coordinator Jobs in Los Angeles

clinical research coordinator

medical assistant - clinical research Jobs in Los Angeles

medical assistant - clinical research

administrative research coordinator Jobs in Los Angeles

administrative research coordinator

research nurse

UCLA Health

<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)

Cedars-Sinai Medical Center

<div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<p>
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.</p>
<p><b>
Join our team and use your skill with an organization known nationally for excellence in research!</b></p>
<p><b>
Job Summary:</b></p>
<p>
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.</p>
<p><b>
Job Duties and Responsibilities:</b></p>
<p>
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.</p>
<p>
Evaluates and abstracts clinical research data from source documents.</p>
<p>
Ensures compliance with protocol and overall clinical research objectives.</p>
<p>
Completes Case Report Forms (CRFs).</p>
<p>
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.</p>
<p>
Provides supervised patient contact or patient contact for long term follow-up patients only.</p>
<p>
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.</p>
<p>
Assists with clinical trial budgets and patient research billing as needed</p>
<p>
Schedules patients for research visits and research procedures.</p>
<p>
Responsible for sample preparation and shipping and maintenance of study supplies and kits.</p>
<p>
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.</p>
<p>
Maintains research practices using Good Clinical Practice (GCP) guidelines.</p>
<p>
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.</p>
<p>
Participates in required training and education programs.</p><br>
<p></p>
<h2 class="jobSectionHeader"><b>Qualifications</b></h2>
<p><b>
Education:</b></p><p>
High School diploma/GED required.</p><p>
BA/BS degree in Science, Sociology or related degree preferred.</p><p><b>
Experience:</b></p><p>
Understanding of general research objectives.</p><p>
1 year of clinical research related experience preferred.</p><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><p>
Physical Demands:</p><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><p></p>

Heart Institute Clinical Research Associate I - Cheng Lab

Cedars-Sinai

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <strong>
  Join us as we translate today's discoveries, into tomorrow's medicine!
  <br/>
  <br/>
 </strong>
 Regenerative medicine is a new and developing field that strives to restore function in diseased or aged tissues through either revitalizing existing cells or transplanting new ones. At the Board of Governors Regenerative Medicine Institute, researchers are turning stem cells into therapies for treating a multitude of prevalent diseases and conditions. We're also exploring how to prevent diseases, and we're extending our knowledge to students in Los Angeles and researchers around the world. To learn more, please visit Board of Governors Regenerative Medicine Institute | Cedars-Sinai
 <br/>
 <br/>
 <strong>
  Are you ready to be a part of breakthrough research?
  <br/>
  <br/>
 </strong>
 The Clinical Research Associate I will work directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. 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. Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. Additionally, this position will include animal work (injections, dissections, and surgery), sample processing, and cell culture.
 <br/>
 <br/>
 <strong>
  Primary Job Duties and Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Completes Case Report Forms (CRFs).
  </li>
  <li>
   Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
  </li>
  <li>
   Provides supervised patient contact or patient contact for long term follow-up patients only.
  </li>
  <li>
   Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
  </li>
  <li>
   Assists with clinical trial budgets.
  </li>
  <li>
   Assists with patient research billing.
  </li>
  <li>
   Schedules patients for research visits and research procedures.
  </li>
  <li>
   Responsible for sample preparation and shipping and maintenance of study supplies and kits.
  </li>
  <li>
   Maintains research practices using Good Clinical Practice (GCP) guidelines.
  </li>
  <li>
   Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  </li>
  <li>
   Participates in required training and education programs.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Department-Specific Duties and Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Performs data searches and other related administrative tasks.
  </li>
  <li>
   Assists with research protocol writing and development.
  </li>
  <li>
   Transportation of research medications.
  </li>
  <li>
   Performs study related assessments and questionnaires.
  </li>
  <li>
   Assists with prescreening of potential research participants for various clinical trials.
  </li>
  <li>
   Maintains organized paper and electronic research files.
  </li>
  <li>
   Performs all data collection and data entry tasks for department clinical trials.
  </li>
  <li>
   Assists with preparing manuscripts, letters, and other research documents as needed.
  </li>
  <li>
   Responds to sponsor&rsquo; inquiries regarding protocol start-up activities and recruitment.
  </li>
  <li>
   Performs literature reviews.
  </li>
  <li>
   Attends research meetings and monthly conference calls with sponsors for study updates.
  </li>
  <li>
   Performs cell culture, immunohistochemistry including processing of samples.
  </li>
  <li>
   Performs animal injections, dissections and surgery.
  </li>
  <li>
   Assists with scheduling of visits and assessments.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   <strong>
    Qualifications
    <br/>
    <br/>
   </strong>
  </strong>
 </strong>
 <strong>
  Education:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   High School Diploma or GED is required.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Experience and Skills:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Clinical Research related experience is preferred.
  </li>
  <li>
   Ability to interpret and apply knowledge of State, Federal, and Agency standards to follow regulations.
  </li>
  <li>
   Must possess digital literacy, including Word and Excel, and the ability to use standard office equipment is required.
  </li>
 </ul>
</div>


Clinical Research Associate I - Regenerative Medicine Institute

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!
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What TRIO Can Offer You
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </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

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!
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 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.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  What TRIO Can Offer You
  <br/>
  <br/>
 </strong>
 <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
   <br/>
   <br/>
  </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.
 <br/>
 <br/>
 Prior to applying please review TRIO's Applicant Information Notice
 <br/>
 <br/>
 To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
 <br/>
 <br/>
 To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.
 <br/>
 <br/>
 Teamwork
 <br/>
 <br/>
 <ul>
  <li>
   Passion
  </li>
  <li>
   Integrity
  </li>
  <li>
   Innovation
  </li>
 </ul>
</div>


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

University of California Los Angeles

<div><div><div><div><div><div>The UCLA Chemistry &amp; Biochemistry Department has a tradition of excellence and is ranked among the best in the country, as evidenced by the quality of its programs, the caliber of its faculty, and the excellence of its students. The Department is a leader in cutting-edge research and innovative educational programs.</div></div><div><div>
The Department employs over 50 professors pursuing research in all areas of chemistry and biochemistry. The goals of this research include synthesizing complex natural products and new nano-materials required to solve the many health and environmental crises facing our planet, and illuminating the molecular mechanisms that regulate the decoding of genetic information.</div></div><br>
<br>
<p><b>Salary &amp; Compensation</b></p><br>
<br>
<ul><li>UCLA provides a full pay range. Actual salary offers consider factors, including budget, prior experience, skills, knowledge, abilities, education, licensure and certifications, and other business considerations. Salary offers at the top of the range are not common. Visit UC Benefit package to discover benefits that start on day one, and UC Total Compensation Estimator to calculate the total compensation value with benefits.
</li></ul><p><b>Qualifications</b></p><br>
<ul><li>
Strong project management skills: budgeting, scheduling, and multi-site coordination (Required)
</li></ul><ul><li>Experience coordinating human-subjects or clinical research with firefighters, including IRB and HIPAA compliance (Required)
</li></ul><ul><li>10+ years of experience interacting and working with fire service personnel, apparatus, and equipmentes. Thorough knowledge of fire department culture, shift schedules, strategy, tactics, and organi (Required)
</li></ul><ul><li>Proficiency with REDCap, Excel, and database management; ability to create SOPs and conduct QA/QC checks (Required)
</li></ul><ul><li>Knowledge of the safe handling and disposal of hazardous chemicals and safe laboratory practices. Knowledge of current state, federal, OSHA regulations as they apply to the assigned tasks. Knowledge of UCLA regulations is strongly preferred. (Required)</li></ul>
<ul><li>Working knowledge of Macintosh desktop computers and common associated software, including Word, Excel and Filemaker Pro. (Required)</li></ul>
<ul><li>Working knowledge of the fire incident command structure; possesesses ICS 100 and ICS 700 Certification (Required)</li></ul>
<ul><li>Advanced laboratory skills including biospecimen processing, Luminex or similar immunoassays, and instrument calibration/maintenance (Required)</li></ul>
<ul><li>2+ years of scientific communication experience with firefighter participants, hosting fire departments and union representatives, co-investigators, support staff. Possesses excellent verbal and written communication skills to convey procedures in a clear concise manner. (Required)</li></ul>
<ul><li>Knowledge of Physical Biochemistry and Organic Chemistry. (Required)</li></ul>
<ul><li>Over 5 years of field research experience with firefighters including human subjects research and environmental sampling techniques and operation of portable air- and surface-sampling equipment (Required)</li></ul>
<br>
<p><b>Education, Licenses, Certifications &amp; Personal Affiliations</b></p><br>
<ul><li>
High School Diploma and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities. (Required)
</li></ul><ul><li>Bachelor's Degree in Health-related or life science field or equivalent experience/training (Preferred)
</li></ul><br>
<p><b>Special Conditions for Employment</b></p><br>
<ul><li>
Background Check: Continued employment is contingent upon the completion of a satisfactory background investigation.</li></ul>
<ul><li>Age Requirement: Candidate(s) must be 18 years or older to be eligible to be hired.</li></ul>
<br>
<p><b>Schedule</b></p><br>
<br>
8 am - 5 pm
<br>
<p><b>Union/Policy Covered</b></p><br>
<br>
RX-Research Support Professionals
<br>
<p><b>Complete Position Description</b></p><br>
<br>
https://universityofcalifornia.marketpayjobs.com/ShowJob.aspx?EntityID=38&amp;JDName=Clinical%20Research%20Coordinator%20(TBD_941032)</div></div></div><div><div><div><p>
Apply</p></div></div></div></div>
<br><div><div><b>Campus Requisition #:</b></div>
<p>10025</p>
<div><b>UC Payroll Title:</b></div>
<p>CLIN RSCH CRD</p>
<div><b>Department:</b></div>
<p>CHEMISTRY AND BIOCHEMISTRY</p>
<div><b>Appointment Type:</b></div>
<p>2 - Staff: Career</p>
<div><b>Anticipated Hiring Pay Scale:</b></div>
<p>$36.37 - $58.52</p>
<ul><li><b>Full Salary Range:</b></li></ul>
<p>USD $36.37/Hr. - USD $58.52/Hr.</p>
<div><b>Onsite | Remote | Hybrid Type:</b></div>
<p>Flexible-To Be Determined</p>
<div><b>Department Location:</b></div>
<p>607 Charles E. Young Dr. East MIMG
</p><div><b>Full or Part Time:</b></div>
<p>Full Time</p></div>

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