laboratory operations coordinator

Children's National Hospital

<div></div><div><div><b>Description</b><div></div><p><br>
Reporting to the Director Research Biomed Operations Engineer the Research Biomed Operation coordinator will provide font line day to day operational support to the Children's National Research Institute's (CNRI) research faculty and staff. The individual will provide customer service to 450+ personnel, support approximately 200,000 square feet of research space and 3000 pieces of research equipment. The position will serve along with the Research Biomed Ops Engineers as the service point of contact for CNRI faculty and staff for any equipment/facility and maintenance related issues. The individual will work with the Research Center staff, Children's National Hospital's facility/engineering department, EVS, the safety office, as well as outside vendors. Additional responsibilities will include assisting the coordination of repairs and maintenance, moves and deliveries; facility inspections and user training in addition to staffing special projects as assigned. The individual will work closely with the Environmental Health &amp; Safety staff.</p><div><br>
</div></div><div><b>
Qualifications</b><div></div><p><b><br>
Minimum Education</b><br>
Associate degree in Electronic Engineering Technology, Mechanical Engineering, Biomedical Engineering Technology, or equivalent-related civilian and/or military experience required. (Required)<br>
Bachelor&rsquo;s degree in engineering, electronics or applicable field, degree in bioengineering preferred (Preferred)<br>
<br>
<b>Minimum Work Experience</b><br>
1-2 years of applicable work or internship experience. A BS degree may be substituted for work experience. Preference may be given to biomedical equipment technicians with experience, and experience working in laboratory environment and/or specifically performing PMs and repair on laboratory equipment. (Preferred)<br>
<br>
<b>Required Skills/Knowledge</b><br>
Knowledge of OSHA and laboratory safety regulations<br>
Within scope of job, requires critical thinking skills, decisive judgement and the ability to work with minimal supervision<br>
Ability to understand and utilize technical vocabulary to perform tasks according to either verbal or written instructions<br>
Ability to display strong organizational and multi-tasking skills, self-discipline, and autonomy to work independently in a high-pressure environment<br>
Must be able to work in a fast-paced environment and take appropriate action<br>
Strong customer service orientation and ability to follow through issues to resolution<br>
Ability to interact with all levels of organizational personnel to include: management staff, consulting staff, researchers, research administrators, etc.<br>
Ability to build consensus and work in a collaborative manner<br>
Ability to maintain accurate records of repairs, calibration, and tests<br>
Must be able to function as part of a team providing a high level of quality service to clients<br>
Knowledge of computers and networking; PC competency to include utilization of Microsoft Office Suite products.<br>
<br>
<b>Functional Accountabilities</b><br>
<b>Responsible Conduct of Research</b></p><br>
<ul><li>
Consistently demonstrates adherence with the standards for the responsible conduct of research</li></ul><ul><li>
Responsible for appropriate use of research funds and resources</li></ul><ul><li>
Comply with all annual job-related training requirements</li></ul><p><b>
Facility Management</b></p><br>
<ul><li>
Work with CNRI leadership to assist with executing assignments of offices and laboratory space.</li></ul><ul><li>
Work with CNH Facility Engineering, EVS, IT, Telecommunication to coordinate implementation of these assignments.</li></ul><ul><li>
Work with CNH Facility Engineering staff to identify and resolve facility deficiencies.</li></ul><ul><li>
Ensure the facility is in compliance with regulatory standards and coordinate corrective actions.</li></ul><ul><li>
Follow up on the work of contractors and staff involved corrective activities</li></ul><ul><li>
Serve as the CNRI liaison with environmental services and monitor facility cleanliness and coordinate corrective action.</li></ul><p><b>
Program Coordination</b></p><br>
<ul><li>
Respond to support requests within established timelines</li></ul><ul><li>
Utilize tools, support, resources, and escalation processes within required time frames to resolve customer and system problems timely and effectively.</li></ul><ul><li>
Interview customer to determine nature and scope of the service issue, and initiate the appropriate response</li></ul><ul><li>
Maintain accurate records of all work performed</li></ul><ul><li>
Coordinate relocations and renovations as assigned and serve as the point of contact for contractors and staff</li></ul><ul><li>
Effectively coordinate projects within the established time tables</li></ul><ul><li>
Oversee the installation of new equipment</li></ul><ul><li>
Demonstrate understanding of customer service policies and procedures, continuously develop depth and breadth of technical competencies.</li></ul><p><b>
Equipment Maintenance</b></p><br>
<ul><li>
Coordinate annual space and equipment survey, update and maintain databases accuracy throughout the year</li></ul><ul><li>
Continually update the CNRI freezer inventory and prepare reports as needed</li></ul><ul><li>
Inform supervisor of equipment status changes in a timely manner</li></ul><ul><li>
Schedule and perform preventive maintenance, performance assurance testing, electrical safety inspections, and schedule repairs to correct failed equipment with outside vendor and CNH staff.</li></ul><ul><li>
Log all CNRI Administration generated work orders and service calls and monitor on time service delivery and quality.</li></ul><ul><li>
Coordinate regular scheduled building inspection with appropriate CNH staff.</li></ul><p><b>
CNRI Common Facility Maintenance</b></p><br>
<ul><li>
Order supplies as needed.</li></ul><ul><li>
Provide in-service education to staff on facility and equipment operation and safety</li></ul><ul><li>
Ensure that equipment is operational and the facility is clean on a daily basis. Identify and coordinate resolutions of service or facility issues.</li><li>
Anticipate and responds to customer needs; follows up until needs are met</li></ul><p><br>
Teamwork/Communication</p><ul><li>
Demonstrate collaborative and respectful behavior</li></ul><ul><li>
Partner with all team members to achieve goals</li></ul><ul><li>
Receptive to others&rsquo; ideas and opinions</li></ul><p><br>
Performance Improvement/Problem-solving</p><ul><li>
Contribute to a positive work environment</li></ul><ul><li>
Demonstrate flexibility and willingness to change</li></ul><ul><li>
Identify opportunities to improve clinical and administrative processes</li></ul><ul><li>
Make appropriate decisions, using sound judgment</li></ul><p><br>
Cost Management/Financial Responsibility</p><ul><li>
Use resources efficiently</li></ul><ul><li>
Search for less costly ways of doing things</li></ul><p><br>
Safety</p><ul><li>
Speak up when team members appear to exhibit unsafe behavior or performance</li></ul><ul><li>
Continuously validate and verify information needed for decision making or documentation</li></ul><ul><li>
Stop in the face of uncertainty and takes time to resolve the situation</li></ul><ul><li>
Demonstrate accurate, clear and timely verbal and written communication</li></ul><ul><li>
Actively promote safety for patients, families, visitors and co-workers</li></ul><ul><li>
Attend carefully to important details - practicing Stop, Think, Act and Review in order to self-check behavior and performance</li></ul><div>
</div></div><div><b>
Primary Location</b><b>:</b> District of Columbia-Washington</div><div><b>
Work Locations</b><b>:</b> Research &amp; Innovation Campus 7144 13th Place NW Washington 20012</div><div><b>
Job</b><b>:</b> Research</div><div><b>
Organization</b><b>:</b> Office Operations &amp; Reg Affair</div><div><b>
Position Status</b><b>:</b> R (Regular) - FT - Full-Time</div><div><b>
Shift</b><b>:</b> Day</div><div><b>
Work Schedule</b><b>:</b> Mon-Fri 8:30am-5pm</div><div><b>
Job Posting</b><b>:</b> Jun 12, 2026, 6:28:35 AM</div><div><b>
Full-Time Salary Range</b><b>:</b> 42702.4 - 71156.8</div></div>

Research Biomed Operations Coordinator

Advanced Research Institute

<p>Job Description Summary: The Clinical Research Coordinator (CRC) works under the direction of company administration and the principle investigator to perform assigned and delegated duties associated with the execution of clinical research trial protocols. The Clinical Research Coordinator will have, or will develop, skills in phlebotomy, electrocardiograms, collection of medical/surgical histories, basic laboratory tests, performance of subject trial visits, completion of case report forms (CRFs), and resolution of data queries. The Clinical Research Coordinator will participate in the completion of regulatory documents. The Clinical Research Coordinator shall have the highest moral and ethical standards and will be expected to conduct themselves in a responsible, professional, moral, and ethical manner at all times. The Clinical Research Coordinator shall have excellent interpersonal communication skills and have a strong commitment to the success of the research team.</p><p>CRC Responsibilities:</p><p>- Assist in the coordination and execution of clinical drug trials under the guidance and direction of the site administrator, principal investigator, and sub-investigators.</p><p>- Read, comprehend, and execute clinical trial protocols.</p><p>- Perform laboratory tests as required by trial protocol.</p><p>- Monitor clinical and laboratory data for accuracy and compliance with trial protocols.</p><p>- Complete all documentation required by trial protocol for submission to the trial sponsor.</p><p>- Comply with all international, federal, state, local, and company guidance, laws, regulations, policies, and procedures as applicable to clinical research trials and Advanced Research Institute.</p><p>- Interact with patients by explaining trial protocols, consenting subjects, monitoring their compliance with protocols, collecting data, and collection laboratory samples.</p><p>- Protect every subject's safety to the best of your ability.</p><p>- Maintain every patient's rights to privacy.</p><p>- Maintain flexibility by performing all other assigned duties.</p><p>-Perform phlebotomy. (Phlebotomist.)</p><p>Training: On the job training. Formal continuing education opportunities provided.</p><p>Experience Requirements: Experience is highly preferred but not necessarily required.</p><p>Education Requirements: High school diploma required.</p><p>Job Type: Full-time</p><p>Schedule:</p><ul><li>8 hour shift</li><li>Monday to Friday</li><li>No weekends</li></ul><p>Ability to commute/relocate:</p><ul><li>Tigard, OR 97223: Reliably commute or planning to relocate before starting work (Required)</li></ul><p>Education:</p><ul><li>High school or equivalent (Required)</li></ul><p>Experience:</p><ul><li>Research: 1 year (Preferred)</li><li>Clinical trials: 1 year (Preferred)</li><li>Phlebotomy: 1 year (Preferred)</li></ul><p>Work Location: In person</p><p>Job Type: Full-time</p><p>Pay: $22.00 - $27.00 per hour</p><p>Benefits:</p><ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Flexible spending account</li><li>Health insurance</li><li>Paid time off</li></ul><p>Ability to Commute:</p><ul><li>Portland, OR 97223 (Required)</li></ul><p>Work Location: In person</p>

Clinical Research Coordinator

NEL & SHEY MEDICAL CENTER AND RESEARCH

<p><b>Job Summary</b><br/>We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our dynamic research team. In this vital role, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and maintaining the integrity of data collection. Your energetic approach will help drive innovative research forward, contributing to advancements in healthcare and patient outcomes. This paid position offers an exciting opportunity to work closely with multidisciplinary teams, coordinate complex studies, and make a meaningful impact in the clinical research field.</p><p><b>Responsibilities</b></p><ul><li>Coordinate all aspects of clinical trials from start-up through closeout, including participant recruitment, scheduling, and follow-up.</li><li>Review and verify study documentation for accuracy, completeness, and regulatory compliance.</li><li>Monitor patient progress by conducting vital signs assessments, blood sampling (phlebotomy), and recording clinical data accurately.</li><li>Manage data collection and entry using electronic medical record (EMR) systems while ensuring adherence to CDISC standards for data formatting.</li><li>Ensure compliance with FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and other applicable protocols.</li><li>Supervise research staff and collaborate with investigators to facilitate smooth trial operations.</li><li>Conduct clinical laboratory procedures and analyze results to support study objectives.</li><li>Maintain detailed documentation review processes, prepare reports, and support audits or inspections as needed.</li><li>Oversee patient safety by monitoring adverse events and ensuring proper reporting procedures are followed.</li><li>Utilize statistical software tools for data analysis to interpret research findings effectively.</li></ul><p><b>Requirements</b></p><ul><li>Proven supervising experience in a clinical research or healthcare setting.</li><li>Strong knowledge of clinical trials management, including FDA regulations and ICH GCP standards.</li><li>Excellent understanding of medical terminology, clinical laboratory procedures, and blood sampling techniques.</li><li>Experience with EMR systems, data management practices, and adherence to CDISC standards.</li><li>Ability to review complex documentation thoroughly while maintaining attention to detail.</li><li>Familiarity with clinical development processes and research methodologies.</li><li>Certification in Good Clinical Practice (GCP) from a recognized issuer for California or equivalent certification is preferred.</li><li>Knowledge of HIPAA compliance requirements related to patient privacy and data security.</li><li>Skills in analysis using statistical software packages are advantageous.</li><li>Effective communication skills for coordinating with multidisciplinary teams and ensuring protocol adherence. Join us as a Clinical Research Coordinator to be at the forefront of groundbreaking healthcare research! Your dedication will help shape the future of medicine while gaining invaluable experience in a fast-paced, rewarding environment dedicated to excellence in clinical trials management.</li></ul><p>Pay: $16.00 - $18.00 per hour</p><p>Work Location: In person</p>

Michigan Orthopaedic and Spine Surgeons

<p><b>Job Summary</b><br/>We are seeking a dynamic and dedicated Clinical Research Coordinator to join our team and drive forward innovative clinical trials. In this vital role, you will oversee the daily operations of clinical studies, ensuring compliance with regulatory standards and maintaining meticulous documentation. Your energetic approach will facilitate smooth trial execution, patient engagement, and data integrity, ultimately contributing to groundbreaking medical advancements. This paid position offers an exciting opportunity to be at the forefront of clinical research, supporting the development of new therapies and treatments.</p><p><b>Responsibilities</b></p><ul><li>Coordinate all aspects of clinical trials from start-up through closeout, ensuring adherence to protocols, FDA regulations, ICH GCP guidelines, and institutional policies.</li><li>Manage patient recruitment, screening, enrollment, and ongoing monitoring to ensure participant safety and protocol compliance.</li><li>Review medical records, laboratory results, and other documentation for accuracy and completeness in accordance with study requirements.</li><li>Conduct patient assessments including vital signs, blood sampling (phlebotomy), and other clinical procedures while maintaining strict confidentiality under HIPAA regulations.</li><li>Utilize electronic medical record (EMR) systems for data entry, management, and reporting; ensure data collection aligns with CDISC standards for clinical research data.</li><li>Supervise research staff and coordinate with multidisciplinary teams to facilitate efficient trial progress.</li><li>Prepare detailed reports, monitor study progress, and assist in audits or inspections by regulatory agencies such as the FDA.</li><li>Ensure compliance with clinical laboratory standards and maintain up-to-date knowledge of clinical development processes.</li></ul><p><b>Skills</b></p><ul><li>Proven supervising experience in a clinical research or healthcare setting with strong leadership capabilities.</li><li>Extensive knowledge of clinical trials management including protocol review, patient monitoring, and data collection procedures.</li><li>Familiarity with medical terminology, blood sampling techniques (phlebotomy), vital signs measurement, and clinical laboratory practices.</li><li>Proficiency in using statistical software for data analysis and interpretation related to clinical studies.</li><li>Deep understanding of FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and compliance management practices.</li><li>Experience working with EMR systems and research databases; ability to manage data accurately according to CDISC standards.</li><li>Certification in Good Clinical Practice (GCP) from a recognized issuer for CA or equivalent; ICH GCP certificate preferred.</li><li>Strong analytical skills with attention to detail in documentation review and data management tasks.</li><li>Background in nursing or related healthcare fields is advantageous; clinical laboratory experience is highly valued. Join us to be part of a passionate team committed to advancing healthcare through meticulous research coordination!</li></ul><p>Pay: $27.00 - $31.00 per hour</p><p>Benefits:</p><ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Work Location: In person</p>

Abu Dhabi Biobank

<div>
 <strong>
  Overview
  <br/>
  <br/>
 </strong>
 The Outreach Coordinator is a key role within the Pan Human Biobank, combining participant engagement with hands‑on responsibility for the lifecycle management of biological specimens. The position supports ethical, compliant, and culturally appropriate recruitment of participants while ensuring the accurate receipt, processing, storage, and tracking of biological samples in accordance with biobank standards.
 <br/>
 <br/>
 Working closely with hospital pre‑processing areas, laboratory reception, logistics, Quality, and clinical teams, the Outreach Coordinator upholds the highest standards of biosafety, data integrity, and regulatory compliance. Through strong collaboration and attention to detail, the role directly contributes to the biobank&rsquo;s mission of enabling high‑quality biomedical research.
 <br/>
 <br/>
 The position may also support specialized biobanking programs, including cord blood and maternal or neonatal collections, where applicable. Regular full‑time attendance during office hours is required, with flexibility for after‑hours work, weekends, on‑call duties, and travel to recruitment or collection sites as needed.
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Lead ethical, culturally appropriate participant recruitment and engagement, including eligibility screening, informed consent, and ongoing participant support in line with regulatory and ethical standards.
  </li>
  <li>
   Build and maintain strong relationships with participants, healthcare providers, institutions, and external stakeholders to support sustained biobank engagement and outreach.
  </li>
  <li>
   Plan and deliver outreach, education, and awareness activities (e.g. information sessions, workshops, community campaigns, events), and represent the biobank at external engagements.
  </li>
  <li>
   Maintain accurate recruitment, training, and participant records within LIMS and other systems, ensuring data integrity, confidentiality, and compliance.
  </li>
  <li>
   Coordinate and support training, education, and engagement initiatives, including materials development, logistics, scheduling, and monitoring effectiveness.
  </li>
  <li>
   Receive, verify, and document biological specimens from collection sites, ensuring correct labeling, documentation, chain‑of‑custody, and alignment with LIMS records.
  </li>
  <li>
   Perform pre‑analytical and specimen processing activities in accordance with SOPs, biosafety standards, and specimen stability requirements, including cold‑chain management.
  </li>
  <li>
   Support quality, inventory, and compliance activities, including incident reporting, corrective actions, audits, and adherence to ISO and biobank regulatory standards.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Life Sciences, Public Health, Nursing, Healthcare Management, or a related field.
  </li>
  <li>
   Minimum of one (1) year of experience in healthcare‑related community engagement, participant recruitment, clinical research, or biobank/research settings.
  </li>
  <li>
   Strong communication and interpersonal skills, with the ability to engage diverse populations respectfully and professionally.
  </li>
  <li>
   Demonstrated understanding of confidentiality, data protection, ethical research practices, and informed consent processes.
  </li>
  <li>
   Knowledge of laboratory practices, biosafety, infection control, and safe handling of biological specimens, including PPE use.
  </li>
  <li>
   Strong organizational, documentation, and record‑keeping skills, with the ability to follow SOPs, manuals, and regulatory guidelines.
  </li>
  <li>
   Proficiency in English and strong computer skills (MS Office and relevant systems); familiarity with LIMS or similar systems is preferred.
  </li>
  <li>
   Additional qualifications such as Arabic language skills, presentation or facilitation experience, laboratory experience, equipment maintenance, advanced research/ethics training, or DOH/DHA licensure are considered an advantage.
  </li>
 </ul>
</div>


Outreach Officer

Combined Health Center Corp

<p><b>Job Overview</b><br/>We are seeking a dynamic and detail-oriented Research Coordinator/Medical Assistant to join our clinical research team. This role is vital in coordinating and supporting clinical trials, ensuring compliance with regulatory standards, and providing exceptional patient care. The ideal candidate will possess a strong foundation in medical terminology, clinical procedures, and research protocols, with a passion for advancing medical knowledge through meticulous data collection and management. This paid position offers an exciting opportunity to contribute to groundbreaking research projects while developing your skills in clinical development and regulatory compliance.</p><p><b>Duties</b></p><ul><li>Assist in the planning, organization, and execution of clinical trials, ensuring adherence to study protocols and regulatory guidelines such as FDA regulations and ICH GCP standards</li><li>Conduct patient monitoring by taking vital signs, performing blood sampling (phlebotomy), and documenting clinical observations accurately within electronic medical records (EMR) systems</li><li>Review and verify study documentation for accuracy, completeness, and compliance with protocol requirements</li><li>Manage data collection, entry, and management using statistical software and CDISC standards to ensure high-quality data integrity</li><li>Support clinical laboratory procedures, including specimen handling and processing, while maintaining strict compliance with HIPAA privacy regulations</li><li>Supervise or assist with research staff training on Good Clinical Practice (GCP) and study-specific procedures</li><li>Monitor patient safety throughout the trial process, including adverse event reporting and compliance management</li><li>Collaborate with investigators, sponsors, and regulatory bodies to ensure smooth trial operations and adherence to all applicable guidelines</li></ul><p><b>Experience</b></p><ul><li>Proven supervising experience in a clinical or research setting, demonstrating leadership in managing teams or projects</li><li>Hands-on experience managing clinical trials from initiation through closeout phases</li><li>Strong knowledge of medical terminology, clinical laboratory procedures, and blood sampling techniques (phlebotomy)</li><li>Familiarity with EMR systems, data management tools, statistical software, and CDISC standards for data collection and analysis</li><li>Understanding of FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and clinical development processes</li><li>Certification in Good Clinical Practice (GCP) from a recognized issuer such as the ICH GCP certificate or equivalent is required; valid certification for California (CA) preferred</li><li>Experience working within clinical research environments involving blood sampling, vital signs assessment, and patient monitoring</li><li>Ability to review complex documentation meticulously while maintaining high standards of compliance and accuracy</li></ul><p>Join us in advancing innovative healthcare solutions! This role offers the chance to work at the forefront of clinical research while honing your skills in a collaborative environment dedicated to excellence. We value motivated professionals eager to make a difference through meticulous research practices combined with compassionate patient care.</p><p>Pay: $35,500.96 - $50,000.00 per year</p><p>Work Location: In person</p>

Research Coordinator/ Medical Assistant

Northwest Texas Healthcare system

<div>Responsibilities:
<div><b>
Northwest Texas Healthcare System</b> is a 495 bed system serving the city of Amarillo and the surrounding region. We offer the ideal combination of traditional values and the most advanced technologies in healthcare, plus the conveniences of big city living in a friendly, smaller-town atmosphere. From the beauty of Palo Duro Canyon and great recreational facilities, to our quality educational system, Amarillo is a great place to live and work.</div><div></div><div><br>
A hospital is only as good as its employees. That's why we're looking for professionals who are dedicated and passionate about their work. We're looking for employees who can add to our culture of<br>
exemplary patient care and personal excellence. We're looking for exceptional professionals who share our vision and values.</div><div><br>
<br>
Visit us online at: https://www.nwths.com/careers</div><div></div><div><b><br>
POSITION</b><b>: Phlebotomist</b></div><div></div><div><br>
POSITION SUMMARY: Under the general supervision of the Phlebotomy Coordinator, the Phlebotomist assumes the responsibility for performing venipunctures, capillary blood specimen collections, point of care testing (POCT), and related procedures under the philosophy, policies and procedures established by the hospital and the Department of Laboratory Services. The Phlebotomist, under the guidance of the Phlebotomy Coordinator, will assist in the training and guidance of phlebotomy students and new employees. These responsibilities encompass the internal functioning of the Department and the integration of the Department into the overall functioning of Northwest Texas Healthcare System. The Phlebotomist supports an organizational culture of Service Excellence and practices the Service Excellence standards to all customer groups.</div><div></div><div><b><br>
JOB DUTIES/RESPONSIBILITIES:</b></div><br>
<div></div><ul><li>
Practices the profession of phlebotomy in the area(s) of assigned responsibility according to accepted standards of practice as outlined by the College of American Pathologists (CAP), CLIA &rsquo;88, Joint Commission on Accreditation of Healthcare Organizations, and other regulatory agencies as appropriate, and according to the approved policies and procedures of the organization, department, and/or the laboratory Medical Director.
</li><li>Participates in and supports a process to measure, assess, and performance improvement in areas of assigned responsibility. Performs phlebotomy and waived testing procedures in assign areas of the laboratory, clinics, outreach facilities, health fairs, and home-bound patient locations optimizing the efficiency and quality of pre-analytical, analytical, and post-analytical laboratory procedures.</li></ul><div></div><div><b><br>
Benefit Highlights:</b></div><ul><li>
Retention Bonus Program if offered.</li><li>
Loan Forgiveness Program if offered.</li><li>
Challenging and rewarding work environment</li><li>
Competitive Compensation &amp; Generous Paid Time Off</li><li>
Excellent Medical, Dental, Vision and Prescription Drug Plans</li><li>
401(K) with company match and discounted stock plan</li><li>
SoFi Student Loan Refinancing Program</li><li>
Career development opportunities within UHS and its 300+ Subsidiaries!
</li><li>More information is available on our Benefits Guest Website: benefits.uhsguest.com</li></ul><div><b>
About Universal Health Services</b></div><div></div><div><i><br>
One of the nation&rsquo;s largest and most respected providers of hospital and healthcare services, Universal Health Services, Inc. (UHS) has built an impressive record of achievement and performance. Growing steadily since its inception into an esteemed Fortune 500&reg; corporation, annual revenues during 2025 were $17.4 billion. In 2026, UHS was again recognized as one of Fortune World&rsquo;s Most Admired Companies&trade; and in 2025, was listed in Forbes ranking of America&rsquo;s Largest Public Companies.</i></div><div></div><div><i><br>
Headquartered in King of Prussia, PA, UHS has approximately 101,500 employees and continues to grow through its subsidiaries. Operating acute care hospitals, behavioral health facilities, outpatient facilities and ambulatory care access points, an insurance offering, a physician network and various related services located in 40 U.S. states, Washington, D.C., Puerto Rico and the United Kingdom. For additional information visit </i><i>www.uhs.com</i></div>
Qualifications:
<div><b>
EDUCATION, TRAINING, EXPERIENCE AND LICENSES/REGISTRATIONS REQUIRED:</b></div><ul><li>
Minimum Education: High school graduation or equivalent required; successful completion of a phlebotomy program preferred</li><li>
Minimum Work Experience: One year of full time experience preferred</li><li>
Certifications: PBT(ASCP) required or eligible (to be obtained within 12 months of employment)</li><li>
Current BLS certification from the American Heart Association upon hire or within 30 days of start date and maintain certification throughout employment. This must be obtained prior to providing patient care</li><li>
Valid Texas Drivers License with no more then 3 moving violations in the past 3 years</li></ul><div></div><div><b><br>
PHYSICAL AND SENSORY REQUIREMENTS:</b></div><ul><li>
Ability to read, write, and converse in English</li><li>
Ability to follow instructions, reason, and make appropriate judgments</li><li>
Ability to perform computer functions accurately and quickly</li><li>
Ability to perceive pertinent details and objects in pictorial or graphic material</li><li>
Ability to perceive pertinent details from verbal and tabular material</li><li>
Ability to coordinate eyes, hands, and fingers in order to make skillful, accurate, and precise movements</li><li>
Ability to communicate with patients, family, staff, physicians, and others</li><li>
Ability to accurately evaluate and interpret information and make independent decisions</li><li>
Ability to cope with and remain calm under stress</li><li>
Ability to speak and hear, to allow discussions with customers, employees, and peers</li><li>
Ability to perceive similarities and differences in color</li><li>
Ability to understand the overall technology, operation, and troubleshooting of moderate and complex instrumentation (example: hospital and laboratory information systems, highly automated specimen processing and testing instrumentation)</li><li>
Ability to perform mathematical operations quickly and accurately</li><li>
Ability to understand and explain the theories of laboratory specimen processing</li><li>
Ability to multi-task productively and accurately</li><li>
Ability to remain focused on job responsibilities</li></ul><div><b>
EEO Statement</b></div><div></div><div><i><br>
All UHS subsidiaries are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants and teammates. UHS subsidiaries are equal opportunity employers and as such, openly support and fully commit to recruitment, selection, placement, promotion and compensation of individuals without regard to race, color, religion, age, sex (including pregnancy, gender identity, and sexual orientation), genetic information, national origin, disability status, protected veteran status or any other characteristic protected by federal, state or local laws.</i></div><div></div><div><b><br>
Avoid and Report Recruitment Scams</b></div><div></div><div><i><br>
We are aware of a scam whereby imposters are posing as Recruiters from UHS, and our subsidiary hospitals and facilities. Beware of anyone requesting financial or personal information.</i></div><div></div><div><i><br>
At UHS and all our subsidiaries, our Human Resources departments and recruiters are here to help prospective candidates by matching skill set and experience with the best possible career path at UHS and our subsidiaries. During the recruitment process, no recruiter or employee will request financial or personal information (e.g., Social Security Number, credit card or bank information, etc.) from you via email. Our recruiters will not email you from a public webmail client like Hotmail, Gmail, Yahoo Mail, etc.</i></div><div></div><div><i><br>
If you suspect a fraudulent job posting or job-related email mentioning UHS or its subsidiaries, we encourage you to report such concerns to appropriate law enforcement. We encourage you to refer to legitimate UHS and UHS subsidiary career websites to verify job opportunities and not rely on unsolicited calls from recruiters.</i></div></div>

Phlebotomist / Lab / FT

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7727 laboratory operations coordinator jobs Near Me

Research Biomed Operations Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Outreach Officer

Research Coordinator/ Medical Assistant

Phlebotomist / Lab / FT