clinical research associate i

University of Texas at Austin

<div><div>Job Posting Title:</div>
Clinical Research Associate I<div>
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Hiring Department:</div>
Department of Psychiatry<div>
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Position Open To:</div>
All Applicants<div>
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Weekly Scheduled Hours:</div>
40<div>
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FLSA Status:</div>
Exempt<div>
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Earliest Start Date:</div>
Immediately<div>
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Position Duration:</div>
Expected to Continue Until May 31, 2026<div>
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Location:</div>
AUSTIN, TX<div>
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Job Details:</div><div>
General Notes</div><div>
This is a grant-funded position with an anticipated end date of May 31, 2026, with the possibility of extension based on availability of funding, work performance, and progress toward research goals.</div><div></div><div>
Purpose</div><div>
The Clinical Research Associate I supports grant-funded research studies in the Lippard Lab within the Department of Psychiatry, with responsibilities spanning participant recruitment, study coordination, clinical and behavioral assessments, MRI data collection, and data management. This role contributes to a collaborative research environment focused on advancing understanding of mental health and behavioral outcomes.</div><div></div><div>
Responsibilities</div><ul><li><div>
Conduct phone screens for study recruitment and assist with subject recruitment.</div></li><li><div>
Conduct clinical and behavioral assessments, including structured clinical interviews, alcohol administration sessions, and MRI scans.</div></li><li><div>
Help with subject management, scheduling and reimbursement, and data analysis.</div></li><li><div>
Other duties as assigned.</div></li></ul><div></div><div>
Required Qualifications</div><ul><li><div>
Bachelor's degree.</div></li><li><div>
Basic engineering and/or scientific equipment ordinarily used in college laboratory work.</div></li><li><div>
Relevant education and experience may be substituted as appropriate.</div></li></ul><div></div><div>
Preferred Qualifications</div><ul><li><div>
Experience with projects involving human subject research.</div></li><li><div>
Experience with REDCap.</div></li><li><div>
Experience with clinical assessments (including structured clinical interviews).</div></li><li><div>
Experience with alcohol administration studies and MRI data collection.</div></li><li><div>
Demonstrated ability to communicate (written and verbal) and interact skillfully with investigators, staff, and researchers</div></li><li><div>
Work both as a team member and independently without continuous supervision</div></li><li><div>
Work with overlapping projects and with sensitive and confidential information</div></li><li><div>
Adapt to a dynamic and deadline-driven, patient-oriented environment.</div></li></ul><div></div><div>
Salary Range</div><div>
$40,000 + depending on qualifications</div><div></div><div>
Working Conditions</div><ul><li><div>
May work in all weather conditions</div></li><li><div>
May work around standard office conditions</div></li><li><div>
May work around biohazards</div></li><li><div>
May work around chemicals</div></li><li><div>
May work around electrical and mechanical hazards</div></li><li><div>
Repetitive use of a keyboard at a workstation</div></li><li><div>
Climbing of stairs</div></li><li><div>
Lifting and moving</div></li><li><div>
Occasional evening, weekend, and overtime work to meet research deadlines</div></li><li><div>
This position is based on-campus and requires regular, in-person attendance during the work week</div></li></ul><div></div><div>
Required Materials</div><ul><li><div>
Resume/CV</div></li><li><div>
3 work references with their contact information; at least one reference should be from a supervisor</div></li><li><div>
Letter of interest</div></li></ul><div></div><div>
Important for applicants who are NOT current university employees or contingent workers: You will be prompted to submit your resume the first time you apply, then you will be provided an option to upload a new Resume for subsequent applications. Any additional Required Materials (letter of interest, references, etc.) will be uploaded in the Application Questions section; you will be able to multi-select additional files. Before submitting your online job application, ensure that ALL Required Materials have been uploaded. Once your job application has been submitted, you cannot make changes.</div><div></div><div>
Important for Current university employees and contingent workers: As a current university employee or contingent worker, you MUST apply within Workday by searching for Find UT Jobs. If you are a current University employee, log-in to Workday, navigate to your Worker Profile, click the Career link in the left hand navigation menu and then update the sections in your Professional Profile before you apply. This information will be pulled in to your application. The application is one page and you will be prompted to upload your resume. In addition, you must respond to the application questions presented to upload any additional Required Materials (letter of interest, references, etc.) that were noted above.</div><div>
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Employment Eligibility:</div>
Regular staff who have been employed in their current position for the last six continuous months are eligible for openings being recruited for through University-Wide or Open Recruiting, to include both promotional opportunities and lateral transfers. Staff who are promotion/transfer eligible may apply for positions without supervisor approval.<div>
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Retirement Plan Eligibility:</div>
The retirement plan for this position is Teacher Retirement System of Texas (TRS), subject to the position being at least 20 hours per week and at least 135 days in length.<div>
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Background Checks:</div><div>
A criminal history background check will be required for finalist(s) under consideration for this position.</div><div>
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Equal Opportunity Employer:</div><div>
The University of Texas at Austin, as an <div>equal opportunity/affirmative action employer</div>, complies with all applicable federal and state laws regarding nondiscrimination and affirmative action. The University is committed to a policy of equal opportunity for all persons and does not discriminate on the basis of race, color, national origin, age, marital status, sex, sexual orientation, gender identity, gender expression, disability, religion, or veteran status in employment, educational programs and activities, and admissions.</div><div>
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Pay Transparency:</div><div>
The University of Texas at Austin will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor&rsquo;s legal duty to furnish information.</div><div>
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Employment Eligibility Verification:</div><div>
If hired, you will be required to complete the federal Employment Eligibility Verification I-9 form. You will be required to present acceptable and original <div>documents</div> to prove your identity and authorization to work in the United States. Documents need to be presented no later than the third day of employment. Failure to do so will result in loss of employment at the university.</div><div>
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E-Verify:</div><div>
The University of Texas at Austin use E-Verify to check the work authorization of all new hires effective May 2015. The university&rsquo;s company ID number for purposes of E-Verify is 854197. For more information about E-Verify, please see the following:</div><ul><li><div>
E-Verify Poster (English and Spanish)</div> [PDF]</li><li><div>
Right to Work Poster (English)</div> [PDF]</li><li><div>
Right to Work Poster (Spanish)</div> [PDF]</li></ul><div>
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Compliance:</div><div>
Employees may be required to report violations of law under Title IX and the Jeanne Clery Disclosure of Campus Security Policy and Crime Statistics Act (Clery Act). If this position is identified a Campus Security Authority (Clery Act), you will be notified and provided resources for reporting. Responsible employees under Title IX are defined and outlined in <div>HOP-3031</div>.</div><div></div><div>
The Clery Act requires all prospective employees be notified of the availability of the Annual Security and Fire Safety report. You may <div>access the most recent report here</div> or obtain a copy at University Compliance Services, 1616 Guadalupe Street, UTA 2.206, Austin, Texas 78701.</div></div>

Clinical Research Associate I

Abbott

<div><p>Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.</p><p><b>
Clinical Research Associate I</b></p><p></p><p><b>
Working at Abbott</b></p><p>
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You&rsquo;ll also have access to:</p><ul><li>
Career development with an international company where you can grow the career you dream of.</li><li>
Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.</li><li>
An excellent retirement savings plan with a high employer contribution</li><li>
Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor&rsquo;s degree.</li><li>
A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.</li><li>
A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.</li></ul><p></p><p><b>
The Opportunity
</b></p><p>The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155.</p><p></p><p>
This is an on-site position in Alameda, California.</p><p></p><p><b>
What You&rsquo;ll Work On</b></p><ul><li>
Perform internal clinical studies, recruit study participants, conduct informed consent discussions with study volunteers, record study data, and maintain study files.</li><li>
Coordinate internal clinical studies from start to close-out.</li><li>
Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items.
</li><li>Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures, and other applicable regulatory requirements.</li><li>
Participate in study start up activities.</li><li>
Assist with shipping study devices and supplies to clinical sites.</li><li>
Perform study device accountability and reconciliation.</li><li>
Assist senior staff in development of study-specific forms and trial-specific monitoring plans.</li><li>
Assist senior staff in study planning, designing case report forms (CRFs), and training of study sites.</li><li>
Maintain and audit Trial Master File (TMF) and upload to eTMF to ensure inspection readiness.</li><li>
Perform review of clinical data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager/Study Lead as needed.
</li><li>Proactively and effectively communicate the status of clinical studies to management.</li><li>
Participate in the interim and final reviews of study data in preparation of regulatory submissions.</li><li>
May interact with RA/QA in responding to audits and FDA inquiries.</li><li>
Perform any other duties as assigned by management.</li></ul><p></p><p><b>
Required Qualifications</b></p><ul><li>
BS degree in life sciences preferred or equivalent with minimum 2 years of as a CRA/CRC/CTA experience, or combination of appropriate education and experience.</li><li>
Experience in conducting medical device studies and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.</li><li>
Perform any other duties as assigned by management.</li><li>
Demonstrate excellence in teamwork, solid interpersonal and communication skills including building rapport with team members/peers, study site staff, and clinical management.</li><li>
Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs</li><li>
Flexibility in daily activities.</li><li>
Proficient with Microsoft Suite</li></ul><p></p><p><b>
Apply Now</b></p><p><b>
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: </b>www.abbottbenefits.com</p><p>
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.</p><p>
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.</p><p></p><p><b>
Divisional Information</b></p><p>
Medical Devices</p><p>
General Medical Devices:</p><p>
Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine ﬁngersticks.</p><p></p><p>
Diabetes</p><p>
We&rsquo;re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We&rsquo;re revolutionizing the way people monitor their glucose levels with our new sensing technology.</p><p></p><p><br>
The base pay for this position is $73,900.00 &ndash; $116,000.00. In specific locations, the pay range may vary from the range posted.</p></div>

Clinical Research, Associate I

Cedars-Sinai Medical Center

<div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<p>
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.</p>
<p>
The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.</p>
Primary Duties and Responsibilities
<ul><li>Works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies.</li>
<li>Collects, evaluates and/or abstracts clinical research data. May assist in designing forms for data collection/abstraction. Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.</li>
<li>Completes Case Report Forms (CRFs). Assists with prescreening of potential research participants for various clinical trials. Schedules research participants for research visits and research procedures. Provides supervised patient contact or independent patient contact for long term follow-up patients only.</li>
<li>Assists supervising staff 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 and patient research billing.</li>
<li>Responsible for sample preparation and shipping and maintenance of study supplies and kits.</li>
<li>Ensures compliance with protocol and overall clinical research objectives. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.</li>
<li>Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.</li>
<li>May serve as one point of contact for external sponsors for select trials. May respond to sponsor inquiries and attend meetings regarding study activity under the direction of supervising staff.</li>
</ul><h2 class="jobSectionHeader"><b>Qualifications</b></h2>
<p><b>
This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.</b></p><p><b>
Requirements:</b></p><ul><li>
High School Diploma/GED required.</li></ul><h2 class="jobSectionHeader"><b>
Preferred:</b></h2><ul><li>
Bachelor's Degree preferred.</li><li>
1 year Clinical research related experience preferred.</li></ul></div>

Clinical Research Associate I, Hybrid

City of Hope

<div><div><p>Join the forefront of groundbreaking research at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.</p><p>
A Clinical Research Associate I role is available under Dr Ravi Salgia, a thoracic oncologist. You will support the clinical and translational research program by performing a broad range of research activities. Clinical duties include patient screening and enrollment, informed consent, protocol coordination, and monitoring across oncology clinical trials. You will be responsible for abstracting and managing clinical, pathological, and outcomes data from electronic health records into research databases, ensuring accuracy and regulatory compliance throughout. This role also involves contributing to the preparation and submission of peer-reviewed manuscripts, conference abstracts, and presentations by conducting literature reviews, compiling data, and supporting writing and revision cycles. Additionally, you will assist in the development of research proposals and grant applications for federal and foundation funding mechanisms, including preparation of supporting documents and coordination of timely submissions. This position offers an excellent opportunity for a motivated professional to contribute meaningfully to impactful oncology research while developing expertise across the full spectrum of clinical research operations.</p><p><b>
As a successful candidate, you will:</b></p><ul><li> Conduct protocol management for an assigned set of multiple research protocols.</li><li> Complete and maintain regulatory documents for IRB, DSMB and PRMC/CPRMC</li><li> Recruit patients to study and establish and maintain relationships with patients, visitors and other hospital personnel, while assuring confidentiality of patient information</li><li> Compile and submit data on appropriate forms according to protocol requirements</li><li> Collect and deliver specimens for analysis using specified equipment and ensure proper labeling.</li></ul></div><div><p><b>
Your qualifications should include:</b></p><ul><li> Associates degree. Experience may substitute for minimum education requirements. Bachelors preferred.</li><li> One year of experience working in a health care setting, preferably in clinical research</li><li> Experience with medical record review, health information systems, and/or clinical trials is preferred</li><li> Superb communication and problem-solving skills and able to function independently and proficiently</li><li> Demonstrable computer skills in Microsoft Word, Excel, and/or Microsoft Access as well as skills in data management and analyses.</li></ul><p><b>
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.</b></p><p><b>
City of Hope is an equal opportunity employer.</b></p><p><b>
To learn more about our Comprehensive Benefits, please </b>CLICK HERE<b>.</b></p></div></div>

Clinical Research Associate I - Thoracic Oncology

ImmunityBio, Inc.

<div>
 <strong>
  Company Overview
  <br/>
  <br/>
 </strong>
 ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient&rsquo;s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient&rsquo;s immune system and treat the host rather than just the disease.
 <br/>
 <br/>
 Why ImmunityBio?
 <br/>
 <br/>
 <ul>
  <li>
   ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
  </li>
  <li>
   Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
  </li>
  <li>
   Work with a collaborative team with the ability to work across different areas of the company.
  </li>
  <li>
   Ability to join a growing company with professional development opportunities.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Position Summary
  <br/>
  <br/>
 </strong>
 The Clinical Research Associate I will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support.
 <br/>
 <br/>
 <strong>
  Essential Functions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Develop, review, and update study-related training materials and documents including site initiation training slides, informed consent form templates, procedures manuals, laboratory and pharmacy manuals
  </li>
  <li>
   Interpret medical and scientific intent of assigned study protocols and study procedures, logistics, risks to research subjects and safety, data evaluation methods etc.
  </li>
  <li>
   Communicate scientific rationale for assigned studies to team members and clinical sites
  </li>
  <li>
   Serve as Subject Matter Expert for clinical sites including providing guidance on protocol interpretation and eligibility requirements
  </li>
  <li>
   Create/edit, distribute and collect site feasibility questionnaires
  </li>
  <li>
   Oversee and support collection of essential documents during study start-up
  </li>
  <li>
   Determine materials and other resources needed to conduct the clinical trial and manage their acquisition and distribution.
  </li>
  <li>
   Collect study and site metrics and maintain study trackers, as needed
  </li>
  <li>
   Conduct case report form (CRF) data review and review of source documents, work with sites to resolve data queries
  </li>
  <li>
   Communicate regularly with field Clinical Research Associates (CRAs) to provide information before and after site visits
  </li>
  <li>
   Partner with field CRAs and CTAs to resolve issues identified during site visits
  </li>
  <li>
   Work with Supply Chain to ensure sites maintain sufficient investigational product (IP) to properly conduct the trial as well as resolve IP temperature monitoring excursions and train or assist sites with corrective actions
  </li>
  <li>
   Train vendors, investigators, and study coordinators on study requirements and provide guidance on site issues
  </li>
  <li>
   Conduct clinical specimen log review, and coordinate shipment of specimens to the sponsor or contracted vendor
  </li>
  <li>
   Train sites on specimen and shipment requirements for central laboratory and serve as liaison with contracted vendors
  </li>
  <li>
   Conduct remote monitoring tasks including reconciliation of site investigational product accountability
  </li>
  <li>
   Provide data listings and compile clinical study report documents to support medical writing activities
  </li>
  <li>
   Create and/or review of slides, overheads, etc., for a project, departmental, sponsor and/or business development presentations
  </li>
  <li>
   Provide support and escalate issues to the Clinical Trial Manager (CTM) as appropriate.
  </li>
  <li>
   Performs ad-hoc and cross-functional duties and/or projects as assigned to support business needs and provide developmental opportunities.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Education &amp; Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in a clinical research, science, or health-related field with 2 years of experience in a clinical research setting; or a high school diploma with 3 years of experience in a clinical research setting required
  </li>
  <li>
   2 years of experience as a Clinical Research Coordinator, Clinical Trial Associate or In-House Clinical Research Associate strongly preferred
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Knowledge, Skills, &amp; Abilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Proficiency in MS Word, Excel, PowerPoint, Outlook, Adobe
  </li>
  <li>
   Excellent written/oral communication skills
  </li>
  <li>
   Strong organizational and multi-tasking skills
  </li>
  <li>
   Maintain corporate confidentiality at all times
  </li>
  <li>
   Ability to set priorities and independent decision making
  </li>
  <li>
   Ability to work independently as well as in teams
  </li>
  <li>
   Strong oral and written communication skills
  </li>
  <li>
   Outgoing and confident demeanor
  </li>
  <li>
   Independent thinker and persuasive communicator
  </li>
  <li>
   Detail oriented, with solid organization and time management skills
  </li>
  <li>
   Completes projects with reliability and minimal guidance
  </li>
  <li>
   Knowledge of drug development process
  </li>
  <li>
   Computer literacy: EDC, eTMF, CTMS, etc.
  </li>
  <li>
   Working knowledge of ICH E6, and the Code of Federal Regulations
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Working Environment / Physical Environment
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This position works remotely with ability to work flexible hours for various time zones
  </li>
  <li>
   Must be able to travel up to 75% of the time based on study requirement.
   <br/>
   <br/>
  </li>
 </ul>
 This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate&rsquo;s qualifications, prior experience as well as geographic location.
 <br/>
 <br/>
 $103,900 (entry-level qualifications) to $114,300 (highly experienced) annually
 <br/>
 <br/>
 The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.
 <br/>
 <br/>
 ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options
 <br/>
 <br/>
 <ul>
  <li>
   Health and Financial Wellness Programs
  </li>
  <li>
   Employer Assistance Program (EAP)
  </li>
  <li>
   Company Paid and Voluntary Life/AD&amp;D, Short-Term and Long-Term Disability
  </li>
  <li>
   Healthcare and Dependent Care Flexible Spending Accounts
  </li>
  <li>
   401(k) Retirement Plan with Company Match
  </li>
  <li>
   529 Education Savings Program
  </li>
  <li>
   Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks
  </li>
  <li>
   Paid Time Off (PTO) includes: 11 Holidays
  </li>
  <li>
   Exempt Employees are eligible for Unlimited PTO
  </li>
  <li>
   Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day
  </li>
  <li>
   We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.
   <br/>
   <br/>
  </li>
 </ul>
 At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.
</div>


Clinical Research Associate I, Field Monitor

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

<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

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