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clinical research associate (data management) - pediatrics - cra neurology research

clinical research associate, iqvia biotech

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business intelligence (bi) developer — engineering analytics Jobs in Houston

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clinical research associate (data management) - pediatrics - cra neurology research Jobs in Houston

clinical research associate, iqvia biotech Jobs in Houston

clinical research associate iqvia biotech

IQVIA

<div>
 <em>
  <strong>
   IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience. Must have experience monitoring in oncology solid tumor.
   <br/>
   <br/>
  </strong>
 </em>
 <em>
  IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
  <br/>
  <br/>
 </em>
 <strong>
  Job Overview
  <br/>
  <br/>
 </strong>
 We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct all types of site visits&mdash;selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
  </li>
  <li>
   Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
  </li>
  <li>
   Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
  </li>
  <li>
   Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
  </li>
  <li>
   Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
  </li>
  <li>
   Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
  </li>
  <li>
   Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
  </li>
  <li>
   Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
  </li>
  <li>
   Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in life sciences or health-related field (or equivalent experience).
  </li>
  <li>
   Requires at least 1 year of on-site monitoring experience.
  </li>
  <li>
   Strong understanding of GCP, ICH guidelines, and regulatory requirements.
  </li>
  <li>
   Ability to travel as required by the project.
   <br/>
   <br/>
  </li>
 </ul>
 IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
 <br/>
 <br/>
 IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
 <br/>
 <br/>
 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
 <br/>
 <br/>
 The potential base pay range for this role, when annualized, is $71,900.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
</div>


Clinical Research Associate, IQVIA Biotech

Baylor College of Medicine

<div><div><div><div><h2 class="jobSectionHeader"><b>Summary</b></h2></div><div><p>
The Clinical Research Associate is responsible for the data management activities of moderate to complex clinical trials and research protocols for the Department of Pediatrics, Research Resource Office (RRO). Primary responsibilities include project management and data reporting of research patient data. Will also contribute to research protocol budget developments, cost assessments, and study reconciliations.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Duties</b></h2></div><div><ul><li>
Independently manages the daily operations of moderate to complex clinical trials and research protocols.</li><li>
Independently manages database of pending and prior clinical trials and research protocols.</li><li>
Provides guidance to investigators and other research staff, and serves as an source of expertise for data management projects, concepts and approaches.</li><li>
Conducts research subject recruitment, screening, and enrollment. Participates in subject consent process.</li><li>
Develops and maintains manual of operations, sop's, and procedural guides/guidelines.</li><li>
Provides budget input and guidance to investigators and other research staff, helping to develop cost assessments, draft budget justifications and complete other budget forms for submission and reporting.</li><li>
Completes data reporting in accordance with good clinical practice, federal regulations and institutional policies:<ul><li>
Oversees regulatory activities, including quality assurance and safety programs.</li><li>
Develops management plans to ensure timeliness and accuracy in data entries and reporting.</li><li>
Oversees submission of serious adverse event reporting and follow-up as needed.</li></ul></li><li>
Assists with expense oversight and study reconciliations.</li><li>
Performs other job-related duties as assigned.<br>
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Minimum Qualifications</b></h2></div><div><ul><li>
Bachelor's degree.</li><li>
Two years of relevant experience.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Preferred Qualifications</b></h2></div><div><ul><li>
Prior experience working in an academic research setting strongly preferred.</li><li>
Ability to understand and manage the complexities of clinical trials and research protocols, including issues related to informed consent, access to data, and conflict of interest.</li><li>
Strong attention to detail and data quality.</li></ul></div></div></div><p></p><p><b><br>
Work Authorization Requirement:</b></p><p><b>
This position is not eligible for visa sponsorship.</b> Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.</p><p></p><p><br>
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.</p></div>

Clinical Research Associate (Data Management) - Pediatrics - CRA Neurology Research

Evolution Research Group

<p></p><div><p><b>Job Title: FT Contract Clinical Research Associate (CRA) needed for Texas; ideal candidate will live in the state of Texas.</b></p><p><b>
This is a FT 6 month+ contract, up to 40 hours per week for the first 3-6 months, then hours will vary based on study.</b></p><p><b>
 Post-operative pain experience required</b></p><p><b>
www.lotuscr.com</b></p><p></p><p><b><br>
Location: Remote</b></p><p><b>
Job Description:</b></p><p>
The Clinical Research Associate conducts site monitoring responsibilities for Clinical trials, according to Standard Operating Procedures, ICH guidelines, and GCP. This is a FT contract role, hours to vary after study is completed.</p><p><b>
Essential Duties and Responsibilities:</b></p><ul><li>
Manage and monitor site activities for assigned clinical studies, working individually or co-monitoring with other Clinical Research Associates (CRAs).</li><li>
Monitoring activities will include but not be limited to site qualification, site initiation, interim monitoring, and close-out visits.</li><li>
During monitoring visits, the CRA ensures compliance with the protocol and applicable Company or Sponsor Standard Operating Procedures (SOPs), FDA regulations, and ICH-GCP guidelines.</li><li>
Perform site evaluation visits of potential investigators. Evaluate the capability of the site to successfully manage and conduct the clinical study.</li><li>
Perform study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the case report forms, monitoring activities and study close-out activities.</li><li>
Assist in resolving any issues to ensure compliance with site file audits.</li><li>
Direct communication with investigational sites on visit planning, query resolution, action item resolution, and any other activities to support site management.</li><li>
Document accountability, stability and storage conditions of clinical trial materials as required by sponsor. Perform investigational product inventory. Ensure return of unused materials to designated location or verify destruction as required.</li><li>
Serve as primary contact with the site; coordinate all correspondence; ensure timely transmission of clinical data with the study site.</li><li>
Perform study close-out visits per the study specific Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.</li><li>
Ensure internal and study-related trainings are completed per Lotus and/or study timelines.</li><li>
Pre and post visit follow up include compliance to timelines indicated in the Monitoring Plan (MP) for Confirmation Letters, Follow up Letters and Monitoring Visit Reports (MVR).</li></ul><p><b>
Education and/or Experience:</b></p><ul><li>
Ability and willingness to travel up to 75% of the time (land and air).</li><li>
College degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).</li><li>
In lieu of the university /college degree or certification requirement, a minimum of<b> 5 years</b> of relevant clinical research experience in health care, pharmaceutical, or CRO settings may be considered and minimum of 2 years field monitoring experience as a CRA.</li><li>
Phase I experience preferred</li><li>
Preferred therapeutic areas: Substance Abuse, MAD/SAD, Hepatic, Impairment, Chronic Pain and Bipolar/Depression.</li><li>
Valid Driver&rsquo;s License.</li><li>
Legally authorized to work in the US.</li></ul><p><b>
Skills and Abilities:</b></p><ul><li>
Proficient knowledge of the drug development process, ICH guidelines, GCP, and the clinical trial process.</li><li>
Experience using electronic CRF platforms and processes.</li><li>
Exceptional attention to detail.</li><li>
Ability to interact effectively within and across team environments.</li><li>
Excellent organizational skills.</li><li>
Proficient computer skills with good working knowledge of a range of standard computer software required (e.g., email, document, spreadsheet, and presentation software).</li></ul></div><p></p>

CRO-Contract Clinical Research Associate (CRA)-Texas (TX)

<div><div><div><div><h2 class="jobSectionHeader"><b>Summary</b></h2></div><div><p>
The Department of Radiation Oncology at Baylor College of Medicine in Houston, TX is recruiting for a position at the Assistant, Associate, or Full Professor level. Physicians are anticipated to take part in all facets of the clinical care, research, and educational mission of the College. Rank and salary based upon experience. This position would focus on Breast and Gynecologic Cancers and the applicant would be expected to participate in the HDR brachytherapy practice. This is a robust gynecologic practice treating &gt;100 patients per year across 4 physician providers and 2 health systems both equipped with new Varian Bravos units. Candidates must have completed their residency in an ACGME-accredited radiation oncology program and/or fellowship in an accredited US training program and have a track record of excellence in clinical care and research.</p><p></p><p><br>
Baylor has been an active part of the radiation oncology community in the Houston area for decades. Through our three current clinical partners, Baylor St Luke's Medical Center, Harris Health, and the Houston VA Hospital, we provide care to a diverse group of patients across the Houston metro area. Baylor College of medicine is a premier academic medical school ranked in the top tier for research and primary care in the US. The Dan L. Duncan Cancer Center is an NCI designated Comprehensive Cancer Center (one of 2 in Houston and 3 in Texas) harboring SPORE grants in both Breast Cancer and Lymphoma while BCM is also home to the Human Genome Sequencing Center. BCM has the highest NIH grant dollars of any center in Texas. A robust research enterprise is available with active participation in NRG, SWOG, and COG.</p><p></p><p><br>
The city of Houston is the 4th most populous city in The United States and its most racially and ethnically diverse major metropolitan area. As such, Houston is home to a vibrant food, music, and theater scene while the museum district alone is home to nineteen galleries, museums, and community spaces. The Texas Medical Center in turn is the largest concentration of medical-related institutions in North America. A total of 54 institutions are represented including: 4 medical schools, seven nursing schools, 8 academic and research institutions, and 21 hospitals. Come explore Space City and see what it has to offer.</p></div></div></div><p></p><p><br>
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.</p></div><p></p>

Physician, Radiation Oncology (Assistant, Associate, or Full Professor)

<div><div><div><div><h2 class="jobSectionHeader"><b>Summary</b></h2></div><div><p>
The Department of Neurology and the Parkinson's Disease Center and Movement Disorders Clinic provide educational programs to residents and fellows, medical students and practicing Neurologists; support research in Neurological disorders; offer the highest quality, and state-of-the-art facilities and equipment. We invite you to learn more about our nationally and internationally recognized physicians and our cutting-edge research.</p><p></p><p><br>
The Parkison&rsquo;s Disease Center &amp; Movement Disorder Clinic is seeking an experienced Senior Research Coordinator who possesses advanced knowledge of clinical research practices. The Senior Research Coordinator will function in a capacity in which they coordinate and facilitate multiple clinical research trials.</p><p></p><p><br>
The Senior Research Coordinator will provide professional skills involving patient-related research efforts. The ideal candidate is expected to perform responsibilities in a manner that promotes quality and safe patient care and customer service; adheres to the scope of practices as defined by the GCP/ICH guidelines.</p><p></p><p><br>
This is a full-time position located at our McNair Campus, in the Texas Medical Center. Learn more about the Department of Neurology Parkinson's Disease Center and Movement Disorders Clinic by using the below link: www.Jankovic.org</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Duties</b></h2></div><div><ul><li>
Coordinates multiple complex clinical research trials, ensuring all study activities are conducted in accordance with protocol requirements, institutional policies, Good Clinical Practice (GCP), and applicable regulatory guidelines. Serves as the primary contact for sponsors, monitors, and investigators during site initiation, interim monitoring, and closeout visits. Educates and informs participants regarding study procedures, expectations, and follow-up requirements. (20%)</li><li>
Oversees participant scheduling and operational flow across assigned trials, ensuring that all study-related tests and procedures (e.g., imaging, laboratory testing, and specialty assessments) are accurately coordinated, documented, and completed within protocol-defined timeframes. Works collaboratively with clinical and ancillary departments to minimize disruptions and optimize participant experience. (10%)</li><li>
Ensures proper collection, processing, shipment, and documentation of research specimens in accordance with protocol requirements and biosafety standards. Ensures chain-of-custody, sample integrity, and timely reporting of lab results. (2%)</li><li>
Maintains and audits regulatory and source documentation for assigned trials to ensure compliance with institutional, sponsor, and federal regulatory requirements. Reviews documentation prepared by junior staff for accuracy and completeness; identifies and addresses gaps proactively. (10%)</li><li>
Oversees investigational product management including receipt, storage, dispensing, reconciliation, and documentation in collaboration with the investigational pharmacy. Ensures compliance with sponsor and FDA requirements for drug accountability. (3%)</li><li>
Performs and oversees advanced clinical procedures as required by protocol, including venipuncture, EKGs/ECGs, vital sign collection, infusion line placement/removal, administration of investigational product (infusion or injection), and continuous monitoring of participants during study drug administration. Ensures team adherence to safety and aseptic standards. (30%)</li><li>
Conducts IRB-related activities, including preparation and submission of new study applications, amendments, continuing reviews, and reports of unanticipated problems. Serves as the departmental resource for IRB process navigation and submission strategy. (5%)</li><li>
Maintains investigational product dispensing and shipping logs in compliance with study protocols and institutional policies. Audits records for accuracy and completeness prior to sponsor review. (3%)</li><li>
Serves as the lead resource and mentor for junior research coordinators, providing training, guidance, and troubleshooting on study conduct, documentation, regulatory compliance, and participant management. Offers input on workflow optimization and operational efficiency across the team. (10%)</li><li>
Represents the research team in meetings with sponsors, CROs, and institutional leadership to address study progress, operational challenges, and compliance matters. Provides input on feasibility assessments for new studies and contributes to strategic planning of departmental research operations. (5%)</li><li>
Performs other related duties as assigned to support the success and compliance of the clinical research program. (2%)</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Other</b></h2></div><div><ul><li>
Conducts detailed discussions with patients regarding study participation, including study purpose, procedures, potential risks and benefits, and patient rights. Obtains informed consent in compliance with FDA, IRB, and institutional requirements, and ensures thorough documentation of the consent process.</li><li>
Ensures the collection, review, and submission of clinical research data through paper and electronic case report forms (CRFs), ensuring data accuracy, consistency, and completeness. Oversees data query resolution and data integrity for assigned trials.</li><li>
Documents study encounters and activities in the electronic medical record (e.g., EPIC or equivalent), ensuring consistency between clinical and research documentation.</li><li>
Leads by example in fostering a culture of compliance, teamwork, and excellence in clinical research operations, contributing to process improvement and departmental efficiency.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Minimum Qualifications</b></h2></div><div><ul><li>
Bachelor's degree in a Basic Science or related field. Four years of related experience may substitute for degree requirement.</li><li>
Five years of relevant experience.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Preferred Qualifications</b></h2></div><div><ul><li>
Master's degree in a related field.</li><li>
Advanced knowledge of clinical research and research processes preferred.</li><li>
Prior experience implementing complex patient studies and protocols.</li><li>
Effective communication skills, both orally and in writing.</li><li>
Interpersonal skills necessary to coordinate research studies.</li><li>
EPIC experience.</li></ul></div></div></div><p></p><p><b><br>
Work Authorization Requirement:</b></p><p><b>
This position is not eligible for visa sponsorship.</b> Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.</p><p></p><p><br>
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.</p></div>

Senior Research Coordinator - Neurology (On Site)

Houston Methodist

<div>At Houston Methodist, the Research Coordinator position is responsible for coordinating the day-to-day activities of research protocols as well as assessing and determining qualification of patients for research studies. This position ensures accurate data collection, documentation, organization and safety of research participants.
<div><b>FLSA STATUS</b><br>
Exempt<br>
<br>
<b>QUALIFICATIONS</b><br>
<br>
<b>EDUCATION</b><ul><li>
Bachelor&rsquo;s degree
</li></ul><br>
<b>EXPERIENCE</b><ul><li>
Two years&rsquo; research experience
</li></ul><br>
<b>SKILLS AND ABILITIES</b><ul><li>
Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going skills, competency assessments, and performance evaluations
</li><li>Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security
</li><li>Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles
</li><li>Sufficient in clinical and research data entry
</li><li>Capable of handling challenging/difficult situations
</li>Demonstrates sound judgment and executes analytical skills<br>
<li>
</li></ul><br>
<br>
<b>ESSENTIAL FUNCTIONS</b><br>
<br>
<b>PEOPLE ESSENTIAL FUNCTIONS</b><ul><li>
Under the direction of higher level staff, conducts screening and interviews to evaluate patient eligibility in study.
</li><li>Promotes a positive work environment and contributes to a dynamic, team focused work unit that actively helps one other to achieve optimal department results. Collaborates with all members of the patient care team by actively communicating and reporting pertinent information as it relates to assigned system(s) in a comprehensive manner.
</li><li>Provides contributions towards improvement of department scores for employee engagement.
</li></ul><br>
<b>SERVICE ESSENTIAL FUNCTIONS</b><ul><li>
Responds promptly and accurately to customer complaints, inquiries, and requests for information and coordinate appropriate follow-up calls and/or appointments.
</li><li>Schedules research subject appointments for tests and procedures, such as laboratory tests, x-rays, and other studies specific for the research protocol.
</li><li>Compiles patient information, process, document and enter accurate information in Source Documents, Case Report Forms, Electronic Data Capture portals and Clinical Trial Management System following established procedures.
</li></ul><br>
<b>QUALITY/SAFETY ESSENTIAL FUNCTIONS</b><ul><li>
Maintains records for clinical study and regulatory documents.
</li><li>Under the direction of Research Nurse/Clinical Trial Manager/Physician, captures and reports Adverse Events (A/E) or Serious Adverse Events (SAE) to necessary regulatory authorities.
</li><li>Assists management with research records and regulatory maintenance.
</li></ul><br>
<b>FINANCE ESSENTIAL FUNCTIONS</b><ul><li>
Uses resources efficiently; does not waste supplies. Evaluates and reports on inventory levels. Self-motivated to independently manage time effectively and prioritize daily tasks.
</li><li>Maintains inventory of supplies necessary for the study.
</li></ul><br>
<b>GROWTH/INNOVATION ESSENTIAL FUNCTIONS</b><ul><li>
Maintains working knowledge of the research process and in the conduct of IRB approved research protocols. Follows International Conference on Harmonization (ICH)/Good Clinical Practice (GCP) guidelines.
</li>Seeks opportunities to expand learning beyond baseline competencies with a focus on continual development. Completes and updates My Development plan on an on-going basis.<br>
<li>
</li></ul><br>
<br>
<b>SUPPLEMENTAL REQUIREMENTS</b><br>
<ul><b>
WORK ATTIRE</b><li><ul><li>
Uniform: No
</li><li>Scrubs: Yes
</li><li>Business professional: No
</li><li>Other (department approved): Yes
</li></ul></li><br>
<b>ON-CALL*</b><br>
<li><ul><li><i>Note that employees may be required to be on-call during emergencies (ie. Disaster, Severe Weather Events, etc) regardless of selection below.</i></li></ul></li><li><ul><li>
On Call* No
</li></ul></li><br>
<b>TRAVEL**</b><br>
<i>**Travel specifications may vary by department**</i><li><ul><li>
May require travel within the Houston Metropolitan area No
</li><li>May require travel outside Houston Metropolitan area No
</li></ul></li></ul></div><b>QUALIFICATIONS</b><br>
<br>
<b>EDUCATION</b><ul><li>
Bachelor&rsquo;s degree
</li></ul><br>
<b>EXPERIENCE</b>
Two years&rsquo; research experience<br>
<ul><li>
</li></ul><br>
<p><b>Company Profile:</b></p><p>
Houston Methodist Academic Institute oversees the Education Institute and Research Institute. The Academic Institute aligns our research and education initiatives in service to the clinical mission, providing solutions that answer the call for new technologies and skills our clinicians need for patient care. Houston Methodist Education Institute coordinates our primary academic affiliation with Weill Cornell Medicine and other joint programs, including the Engineering Medicine Program at Texas A&amp;M University Intercollegiate School of Engineering Medicine. The Education Institute also oversees continuing medical education and graduate medical education, and supports trainees in residence for medical, nursing, allied health and research education programs. Houston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports clinical research protocols and extramurally funded translational research programs.</p><p>
Houston Methodist is an Equal Opportunity Employer.</p></div>

Research Coordinator I

Texas Children's Hospital

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 We are searching for a Patient Care Assistant&mdash; someone who works well in a fast-paced setting. In this position, you will perform a variety of routine and specialized patient care activities, as assigned, under the direction and supervision of the Registered Nurse (RN). Care will be delivered that incorporates Family Centered Care cost-effectively and is developmental and age-appropriate for the patient population.
 <br/>
 <br/>
 Think you&rsquo;ve got what it takes?
 <br/>
 <br/>
 <strong>
  Job Duties &amp; Responsibilities
  <br/>
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assist with the collection and documentation of patient/family data
  </li>
  <li>
   Obtains and documents vital signs (without the use of continuous physiologic monitors) and notifies professional of abnormal findings as evidenced by supervisory observation and review of medical records
  </li>
  <li>
   Provide high-quality, cost-effective patient care in collaboration with the RN and in conjunction with the patient/family
  </li>
  <li>
   Demonstrate ability to collaborate with multiple RNs in a professional manner to prioritize workload based on patient/family needs as evidenced by supervisory observation and verbal/written feedback
  </li>
  <li>
   Assist in identifying patient/family response to care provided
  </li>
  <li>
   Provide input to the RN for the development and ongoing modification of the plan of care, as evidenced by supervisory observation, verbal/written feedback, and review of the plan of care
  </li>
  <li>
   Maintain accountability for development of self and participates in development of others
  </li>
  <li>
   Demonstrate commitment to team, flexibility, professional interpersonal, communication, and customer service skills
  </li>
  <li>
   Participate in achieving hospital/unit goals
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <em>
  As part of our commitment to maintaining a safe and healthy workplace, all successful candidates will be required to undergo respiratory fit testing in compliance with occupational health and safety standards.
  <br/>
  <br/>
 </em>
 <strong>
  Skills &amp; Requirements
  <br/>
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   H.S. Diploma or GED Required
  </li>
  <li>
   One of the following is required in addition to the high school diploma or GED:
  </li>
  <ul>
   <li>
    Completion of a formal nursing assistant educational program or certification (e.g.
   </li>
   <li>
    Diploma/Course/Certificate/associate degree/Etc. completed in a Certified Nurse Assistant, Medical Assistant, or similar clinical education program).
   </li>
   <li>
    Currently enrolled in a BSN degree program with one clinical rotation completed at hire.
   </li>
   <li>
    One (1) year of direct patient care experience.
    <br/>
    <br/>
    <br/>
   </li>
  </ul>
 </ul>
 <strong>
  About Us
  <br/>
  <br/>
 </strong>
 Since 1954, Texas Children&rsquo;s has been leading the charge in patient care, education and research to accelerate health care for children and women around the world. When you love what you do, it truly shows in the smiles of our patient families, employees and our numerous accolades such as being consistently ranked as the best children&rsquo;s hospital in Texas, and among the top in the nation by U.S. News &amp; World Report as well as recognition from Houston Business Journal as one of this city&rsquo;s Best Places to Work for ten consecutive years.
 <br/>
 <br/>
 Texas Children&rsquo;s comprehensive health care network includes our primary hospital in the Texas Medical Center with expertise in over 40 pediatric subspecialties; the Jan and Dan Duncan Neurological Research Institute (NRI); the Feigin Tower for pediatric research; Texas Children &rsquo; s Pavilion for Women, a comprehensive obstetrics/gynecology facility focusing on high-risk births; Texas Children &rsquo; s Hospital West Campus, a community hospital in suburban West Houston; Texas Children &rsquo; s Hospital The Woodlands, the first hospital devoted to children &rsquo; s care for communities north of Houston; and Texas Children&rsquo;s Hospital North Austin, the new state-of-the-art facility providing world-class pediatric and maternal care to Austin and Central Texas families. We have also created Texas Children &rsquo; s Health Plan, the nation &rsquo; s first HMO focused on children; Texas Children &rsquo; s Pediatrics, the largest pediatric primary care network in the country; Texas Children &rsquo; s Urgent Care clinics that specialize in after-hours care tailored specifically for children; and a global health program that is channeling care to children and women all over the world. Texas Children &rsquo; s Hospital is affiliated with Baylor College of Medicine, one of the largest, most diverse and successful pediatric programs in the nation.
 <br/>
 <br/>
 To join our community of 15,000+ dedicated team members, visit texaschildrenspeople.org for career opportunities.
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 Texas Children&rsquo;s is proud to be an equal opportunity employer. All applicants and employees are considered and evaluated for positions at Texas Children's without regard to mental or physical disability, race, color, religion, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status or any other protected Federal, State/Province or Local status unrelated to the performance of the work involved.
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Patient Care Assistant - ACHD

Explore 236+ Clinical research associate iqvia biotech in Houston this April. Find roles across top companies and apply now to boost your career.