clinical research tech

Buck Institute for Research on Aging

<div>
 <strong>
  NOTE: This is a part-time position (15 - 19 hours per week).
  <br/>
  <br/>
  Position Summary
  <br/>
  <br/>
 </strong>
 The Buck Institute for Research on Aging is seeking a
 <strong>
  part-time Clinical Research Technician
 </strong>
 to support the Newman Lab&rsquo;s clinical trial team. This role is ideal for someone detail-oriented, technically skilled, and interested in contributing to human clinical research in a dynamic translational science environment.
 <br/>
 <br/>
 This position supports an observational, longitudinal study designed to map and characterize human biorhythms. The Technician will assist with study visits, participant assessments, biospecimen collection and processing, laboratory preparation, and study documentation. The role is essential to the accurate execution of research procedures and the integrity of study data, with all work conducted in accordance with IRB-approved protocols, Good Clinical Practice, and established standard operating procedures.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
  Clinical Research Support
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assist with standardized participant assessments during study visits, including anthropometric measurements such as height, weight, body composition, and waist circumference
  </li>
  <li>
   Assist with collection of vital signs, including heart rate, oxygen saturation, temperature, and blood pressure
  </li>
  <li>
   Support physical testing procedures, including cardiopulmonary exercise testing, spirometry, grip strength testing, and leg press testing
  </li>
  <li>
   Support challenge visits, including oral glucose tolerance testing and maximal exercise testing
  </li>
  <li>
   Laboratory and Biospecimen SupportAssist with study wearables and devices, including setup, issuance, maintenance, and data synchronization for tools such as continuous glucose monitors, smart wristbands, smart rings, and smart scales
  </li>
  <li>
   Assist with administration and scoring of selected study questionnaires and cognitive testing materials
  </li>
  <li>
   Maintain accurate and complete case report forms and source documentation
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Laboratory and Biospecimen Support
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Prepare and maintain laboratory reagents, collection kits, and supplies needed for study procedures
  </li>
  <li>
   Assist with collection and handling of biospecimens, including venous blood, urine, buccal swabs, stool samples, and vaginal swabs
  </li>
  <li>
   Support biospecimen processing, labeling, storage, and inventory management
  </li>
  <li>
   Package and ship biospecimens to certified external clinical laboratories for analysis
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compliance and Operations
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Maintain a clean, organized, and safe clinical and laboratory environment
  </li>
  <li>
   Support study compliance activities, including maintenance of training records and study documentation
  </li>
  <li>
   Follow IRB-approved protocols, Good Clinical Practice guidelines, and standard operating procedures
   <br/>
   <br/>
  </li>
 </ul>
 Qualifications
 <br/>
 <br/>
 <strong>
  Required
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   High school diploma or equivalent
  </li>
  <li>
   Strong interest in biology, physiology, health sciences, clinical research, or a related field
  </li>
  <li>
   Excellent attention to detail and organizational skills
  </li>
  <li>
   Ability to follow research protocols and maintain accurate records
  </li>
  <li>
   Ability to work on-site during part-time weekday day and evening shifts
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Prior laboratory, clinical, or clinical research experience
  </li>
  <li>
   Experience working with human subjects research
  </li>
  <li>
   Experience with phlebotomy or other clinical procedures
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Compensation and Benefits
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   $24&ndash;$28 per hour
  </li>
  <li>
   Part-time, on-site position
  </li>
  <li>
   Monday&ndash;Friday, day and evening shifts
  </li>
  <li>
   401(k) eligibility with 5% employer match after one year
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About the Buck Institute
  <br/>
  <br/>
 </strong>
 The Buck Institute for Research on Aging is the world&rsquo;s leading independent research institute focused on extending human healthspan. Located in Marin County, California, the Buck brings together scientists across disciplines to better understand and prevent age-related disease.
 <br/>
 <br/>
 The Buck Institute is an equal opportunity employer.
 <br/>
 <br/>
 <strong>
  How To Apply
  <br/>
  <br/>
 </strong>
 Please submit your resume and a cover letter describing your interest in the position and your relevant experience.
</div>


Clinical Research Technician - Newman lab

Mindr

<div><p><b>Who We Are:</b></p>
<p>
At <b>Mindr</b> and our family of brands, we are dedicated to being a force for good. That's why we provide substance use safety, detection and monitoring products and services that help people live responsibly and keep communities safe.</p>
<p><b>
Always aware. Always Guiding. Never Restricting or Judging.</b></p>
<p><b>
What You&rsquo;ll Be Doing</b></p>
<p>
A Clinical Field Technician is responsible for traveling to various residential locations throughout the valley and following established research protocol with study participants. You will have a crucial role in supporting clinical research studies by performing a range of tasks related to data collection and study coordination while keeping participant safety and study confidentiality a top priority.</p>
<ul>
<li>Assists in the conduct of clinical research studies or trials following established protocols and standard operating procedures.</li>
<li>Conducts routine experiments and/or coordinates research study procedures in accordance with SOPs; receives, collects, and records study data in database; communicates and keeps researchers and/or PI up to date on any problems or concerns related to there search study or trial.</li>
<li>Responsible for collecting clinical samples for research including any storage and transportation measures.</li>
<li>Ensures proper documentation of Case Report Forms, regulatory documents, PI notes, and any other mandatory study-related documents and ensures quality and accuracy; archives documents for study per sponsor, government, and institutional requirements;keeps accurate records and provides necessary documents for regulatory audits.</li>
<li>Maintains and manages inventory and research study supplies.</li>
<li>Identify areas to improve research protocol and suggest solutions for implementation.</li>
<li>All other duties as assigned.</li>
</ul>
<p>Day-to-Day Tasks:</p>
<ul>
<li>Clinical study facilitation and data collection (50%)</li>
<li>Travel and transportation (30%)</li>
<li>Study inventory management (10%)</li>
<li>Study process improvements (10%)</li>
<li>All other duties as assigned.</li>
</ul>
<p><b>What You&rsquo;ll Bring to the Table:</b></p>
<ul>
<li>Completed college coursework in relevant STEM disciplines.</li>
<li>Vehicle insurance</li>
<li>Flexible work hours; Set schedule will be negotiated, but must be able to work Sundays, Wednesdays, and Thursdays (25-30 hours/week)</li>
<li>Able to report into our office in downtown Phoenix at start of shift</li>
<li>Proficient communication skills.</li>
<li>High degree of professionalism.</li>
<li>Previous experience in laboratory or clinical trial visits preferred</li>
<li>CITI certification preferred</li>
<li>Must be okay with legal and responsible use of marijuana</li>
</ul>
<p><b>Why work for us?</b></p>
<p><b>
Check out this list of a few of the many good reasons why we are a Top Workplace:</b></p>
<ul>
<li>Salary range is $21.00-$23.00/hr</li>
<li>We are the nation&rsquo;s largest interlock provider, and our Mission is to help people live and drive responsibly.</li>
<li>Mindr won the 2025 Top Workplace Award locally and nationally&ndash;and 2026 Best Place for Working Parents Award</li>
<li>Growth Oriented- 7 years of over 10%+ growth annually. Doubled in employee size over the past 2-3 years.</li>
<li>Ongoing Professional Training &amp; Development</li>
<li>And more</li>
</ul>
<p><b>Equal Opportunity Employer</b></p>
<p>
It is and will continue to be the policy of CST, LLC to practice a program of equal employment opportunity designed to assure that employment and advancement opportunities are made available to all employees and applicants on the basis of individual qualifications and without unlawful regard to race, religion, color, veteran status, national origin, disability, age, gender identity, sexual orientation, sex or genetic information.</p></div>

Research Assistant - Clinical Field Tech (Part-Time) - Phoenix, AZ (On-Site)

The University of Michigan

<p></p><div><div><div><h2 class="jobSectionHeader"><b>Job Summary</b></h2><p>
The Section of Thoracic Surgery is one of seven sections within the Department of Surgery at the University of Michigan Medical School. The Section of Thoracic Surgery is dedicated to setting the standard for teamwork, compassion, education, and innovation as we achieve outstanding outcomes for patients, and create a legacy of excellence in the field through advanced medical training. The Section of Thoracic Surgery is seeking a highly qualified candidate to support the research work of the Thoracic Surgery faculty. The ideal candidate must exercise initiative, judgment, and discretion and be able to prioritize work and make decisions independently. The ability to work as part of a team is essential to the success of a person in this position.</p><h2 class="jobSectionHeader"><b>
Responsibilities*</b></h2><ul><li>
Telephone activity includes contacting potentially eligible study participant to inquire about<br>
interest in participating in research studies. In addition to screening and confirming eligibility,<br>
this role will also contact enrolled patients and conduct follow-up screening and interviews.<br>
</li><li>
Conducting virtual consenting of study participants. This role will use SignNow to push<br>
consent documents to participants who have agreed to receive the consent document for<br>
review and to obtain signature of patients who agree to consent to a study. This role will<br>
also be responsible to image signed consent documents into the participant's medical<br>
record.<br>
</li><li>
Send baseline PROMIS surveys to outcomes research participants.<br>
</li><li>
Assist study coordinator in tracking participants and study progress. Maintain detailed<br>
record-keeping, data entry, and verification of study data. Collection and processing of<br>
biological materials (surgical tissue, blood, saliva, lung washings).</li><li>
Screen, recruit and consent eligible study participants who are present in clinic for thoracic<br>
surgery clinical consultations.</li><li>
Assist Project Manager with regulatory activities</li><li><p>
Experience as part of a team with all 8 competency domains is expected:</p><ul><li>
Scientific Concepts and Research Design</li><li>
Ethical Participant Safety Considerations</li><li>
Investigational Products Development and Regulation</li><li>
Clinical Study Operations (GCPs)</li><li>
Study and Site Management</li><li>
Data Management and Informatics</li><li>
Leadership and Professionalism</li><li>
Communication and Teamwork</li></ul></li></ul><h2 class="jobSectionHeader"><b>
Required Qualifications*</b></h2><p>
Associate degree in Health Science or an equivalent combination of related education and experience is necessary.</p><p>
Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA?s Definition of a Clinical Research Professional for qualifying experience prior to applying.)</p><p>
or</p><p>
An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.</p><p><br>
or</p><p><br>
Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
</p><h2 class="jobSectionHeader"><b>Desired Qualifications*</b></h2><p>
Bachelor?s degree in Health Science or an equivalent combination of related education and experience is desirable.</p><p>
An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.?</p><h2 class="jobSectionHeader"><b>
Why Join Michigan Medicine?</b></h2><p>
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.</p><p><b>
What Benefits can you Look Forward to?</b></p><ul>
<li>Excellent medical, dental and vision coverage effective on your very first day</li>
<li>2:1 Match on retirement savings</li></ul><h2 class="jobSectionHeader"><b>
Modes of Work</b></h2><p>
Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.</p><h2 class="jobSectionHeader"><b>
Background Screening</b></h2><p>
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.</p><h2 class="jobSectionHeader"><b>
Application Deadline</b></h2><p>
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.</p><h2 class="jobSectionHeader"><b>
U-M EEO Statement</b></h2><p>
The University of Michigan is an equal employment opportunity employer.</p></div></div></div><p></p>
<br><div><div><h3 class="jobSectionHeader"><b>Job Opening ID</b></h3>
<div><p>277329</p>
</div></div><div><h3 class="jobSectionHeader"><b>Working Title</b></h3>
<div><p>Clinical Research Technician</p>
</div></div><div><h3 class="jobSectionHeader"><b>Job Title</b></h3>
<div><p>Clinical Research Technician</p>
</div></div><div><h3 class="jobSectionHeader"><b>Work Location</b></h3>
<div><p>Ann Arbor Campus</p>
</div></div><p>Ann Arbor, MI</p>
<div><h3 class="jobSectionHeader"><b>Modes of Work</b></h3>
<div><p>Onsite
</p></div></div><div><h3 class="jobSectionHeader"><b>Full/Part Time</b></h3>
<div><p>Full-Time</p>
</div></div><div><h3 class="jobSectionHeader"><b>Regular/Temporary</b></h3>
<div><p>Regular</p>
</div></div><div><h3 class="jobSectionHeader"><b>FLSA Status</b></h3>
<div><p>Nonexempt</p>
</div></div><div><h3 class="jobSectionHeader"><b>Organizational Group</b></h3>
<div><p>Medical School</p>
</div></div><div><h3 class="jobSectionHeader"><b>Department</b></h3>
<div><p>MM Thoracic Surgery Section</p>
</div></div><div><h3 class="jobSectionHeader"><b>Posting Begin/End Date</b></h3>
<div><p>5/08/2026 - 5/15/2026</p>
</div></div><div><h3 class="jobSectionHeader"><b>Career Interest</b></h3>
<div><p>Research</p></div></div></div>

Clinical Research Technician

IQVIA

<div>
 <em>
  <strong>
   IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. 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>
 The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring high‑quality clinical data, and maintaining study integrity.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 As a CRA I, you will conduct various types of monitoring visits&mdash;including site selection, initiation, routine monitoring, and close‑out visits&mdash;to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).
 <br/>
 <br/>
 A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address site‑level challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or start‑up activities based on study needs.
 <br/>
 <br/>
 Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, follow‑up letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.
 <br/>
 <br/>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree required; a scientific or healthcare discipline is preferred.
  </li>
  <li>
   6 months &ndash;2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
  </li>
  <li>
   Basic knowledge of clinical research regulations (GCP/ICH).
  </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 - $119,900.00. 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>


CRA 1, IQVIA Biotech

Fortrea

<div><p>As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.<br>
<br>
Are you a Certified Nursing Assistant, Medical Technician, Medical Assistant looking for a new opportunity? Take the next step and explore the options available as a Research Technician by joining our team here at Fortrea!</p><p><br>
This is a full-time <b>rotating shift and some weekends, office-based position in Daytona Beach, FL. A schedule will be given in advance.</b></p><p><b><br>
WHAT YOU WILL DO</b></p><p>
Interact directly with our healthy volunteer participants while learning to read clinical research protocols, and enjoy working in a fast-paced, team-oriented environment.<br>
<br>
<b>Other key responsibilities</b>:</p><ul><li><p>
Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings.</p></li><li><p>
Preparation and accurate recording of ECGs/Holters.</p></li><li><p>
Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples.</p></li><li><p>
Monitors meals to ensure dietary compliance by research participants.</p></li><li><p>
Assist in the preparation of rooms and medical equipment.</p></li><li><p>
Assist with screening procedures as needed.</p></li><li><p>
Maintain a clean, safe, and efficient working and study environment.</p></li><li><p>
Other duties as assigned.</p></li></ul><p></p><p><b>
YOU NEED TO BRING&hellip;</b></p><ul><li><p>
High School Diploma or equivalent.</p></li><li><p>
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.</p></li><li><p>
EMT, CMA or CNA certification, preferred.</p></li><li><p>
Phlebotomy experience required.</p></li><li><p>
1 year of related experience.</p></li></ul><p></p><p>
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.</p><p></p><p><b>
Work Environment:</b></p><ul><li><p>
Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.</p></li><li><p>
Occasional drives to site locations, occasional domestic travel.</p></li><li><p>
Exposure to biological fluids.</p></li><li><p>
Personal protective equipment required such as protective eyewear, garments, and gloves.</p></li></ul><p></p><p><b>
Physical Requirements:</b></p><ul><li><p>
Ability to work in an upright and /or stationary position for 6-8 hours per day.</p></li><li><p>
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.</p></li><li><p>
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.</p></li><li><p>
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.</p></li><li><p>
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.</p></li><li><p>
Regular and consistent attendance.</p></li><li><p>
Varied hours may be required.</p></li></ul><p></p><p>
The important thing for us is you are comfortable working in an environment that is:</p><ul><li><p><b>
Fast paced</b>: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.</p></li><li><p><b>
Changing priorities constantly</b> asking you to prioritize and adapt on the spot.</p></li><li><p><b>
Teamwork </b>and<b> people skills</b> are essential for the study to run smoothly.</p></li><li><p><b>
Technology based</b>. We collect our data directly into an electronic environment.</p></li></ul><p></p><p><b>
What do you get?</b></p><p>
Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:</p><ul><li><p>
Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)</p></li><li><p>
401(K)</p></li><li><p>
Paid time off (PTO)</p></li><li><p>
Employee recognition awards</p></li><li><p>
Multiple ERG&rsquo;s (employee resource groups)</p></li></ul><p></p><p>
Learn more about our EEO &amp; Accommodations request here.</p></div>

Clinical Research Technician / Daytona Beach, FL (On-Site)

QPS Holdings, LLC

<div>The Clinical Research Technician position offers flexible hours and a rewarding work environment in the drug research field. This position is primarily responsible for monitoring the study volunteers and ensuring the clinical study is being recorded, conducted, and reported in agreement with the study requirements. This position offers variety, and no two days are alike. The hours are scheduled on an as needed basis and can range from 0-29 hours per week. The essential duties are:<ul><li>
Read and understand study documents, time and events, study restrictions and expectations of sponsor.</li><li>
Check in/out study volunteers and monitor their behavior for study compliance, safety, adverse events and concerns.</li><li>
Perform essential study duties such as recording mealtimes, performing vitals and recording results.</li><li>
Review raw data to ensure accuracy.</li><li>
Help to supervise events to ensure studies are done on time and in accordance with SOPs and Protocols.</li><li>
Maintain cleanliness of the clinics and all study-related areas.</li></ul><p><b>
Experience</b></p><ul><li>
High school diploma or equivalent</li><li>
Outstanding customer service skills</li><li>
High attention to detail</li><li>
Ability to work weekends is desirable</li><li>
Ability to work flexible hours</li></ul><p>
Please visit Recruitment (adp.com) to apply for this position through the company website.</p><p></p><p><br>
QPS Bio-Kinetic (BKCA) provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, QPS Bio-Kinetic (BKCA) complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.</p></div>

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10000 clinical research tech jobs Near Me

Clinical Research Technician - Newman lab

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Clinical Research Technician / Daytona Beach, FL (On-Site)

Clinical Research Technician

CRA 1, IQVIA Biotech