research assistant

University of North Carolina at Chapel Hill

<div><div><div>Posting Information
</div><p></p><div><div><div><div><b>Department</b></div> <div>Peace War and Defense - 316200</div>
</div><br>
<div><div><b>Career Area </b></div><div>Research Professionals</div>
</div><br>
<div><div><b>Posting Open Date</b></div> <div>08/03/2026</div>
</div><br>
<div><div><b>Application Deadline</b></div> <div>08/07/2026</div>
</div><br>
<div><div><b>Position Type</b></div> <div>Temporary Staff (SHRA)</div>
</div><br>
<div><div><b>Position Title </b></div><div>Research Assistant</div>
</div><br>
<div><div><b>Position Number</b></div> <div>20076822</div>
</div><br>
<div><div><b>Vacancy ID</b></div> <div>S027899</div>
</div><br>
<div><div><b>Full-time/Part-time</b></div> <div>Part-Time Temporary</div>
</div><br>
<div><div><b>Hours per week</b></div> <div>8</div>
</div><br>
<div><div><b>Work Schedule</b></div>
<div>Flexible</div>
</div><br>
<div><div><b>Position Location</b></div> <div>North Carolina, US</div>
</div><br>
<div><div><b>Hiring Range</b></div> <div>$20.00 per hour</div>
</div><br>
<div><div><b>Proposed Start Date</b></div> <div>08/10/2026</div>
</div><br>
<div><div><b>Estimated Duration of Appointment</b></div> <div>6 months or longer</div>
</div><br>
</div></div></div><div><div>Position Information
</div><p></p><div><div><div><div><b>Be a Tar Heel!</b></div>
<div><div>A global higher education leader in innovative teaching, research and public service, the <b>University of North Carolina at Chapel Hill</b> consistently ranks as <b>one of the nation&rsquo;s top public universities</b>. Known for its beautiful campus, world-class medical care, commitment to the arts and top athletic programs, Carolina is an ideal place to teach, work and learn.</div><div>
One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.</div><div>
University employees can choose from a wide range of <b>professional training opportunities</b> for career growth, skill development and lifelong learning and enjoy <b>exclusive perks</b> that include numerous retail and restaurant discounts, savings on local child care centers and special rates for performing arts events.<br>
<br>
This position may be eligible for a hybrid work arrangement that may include a partially remote work location, consistent with System Office policy. UNC-Chapel Hill employees are generally required to reside within a reasonable commuting distance of their assigned duty station.<br>
</div></div>
</div><br>
<div><div><b>Primary Purpose of Organizational Unit</b></div>
<div>Peace and war are among the oldest dreams and most difficult challenges of human experience. The curriculum brings together faculty and courses from many disciplines to provide undergraduates with a range of approaches to the fundamental issues of human conflict and national and global security and defense.</div>
</div><br>
<div><div><b>Position Summary</b></div>
<div>The temporary research assistant will support the Director of Undergraduate Studies and Assistant Chair. The research assistant will scour national security news to provide curriculum support to PWAD 250, PWAD 359, PWAD 50, and PWAD 680. The research assistant will also help with piloting PWAD 400, &lsquo;Briefing for National Security.&rsquo;</div>
</div><br>
<div><div><b>Minimum Education and Experience Requirements</b></div>
<div>Demonstrated possession of the competencies necessary to perform the work.</div>
</div><br>
<div><div><b>Management Preferences</b></div>
<ul><li>Superior organization and communication skills</li><li>PWAD experience</li><li>Experience providing undergraduate curriculum</li></ul>
</div><br>
<div><div><b>Special Physical/Mental Requirements</b></div>
</div><br>
<div></div><div><div><b>Campus Security Authority Responsibilities</b></div>
<p>Not Applicable.</p></div></div></div></div></div><p></p>

Research Assistant

Marshall University

<div><div>The Sidarala Laboratory is seeking a highly motivated Research Assistant to join a dynamic research program focused on understanding how mitochondrial dynamics regulates pancreatic &beta;-cell function, aging, and diabetes. The successful candidate will contribute to projects investigating the cellular and molecular mechanisms underlying type 2 diabetes using cutting-edge molecular biology and imaging approaches.<br>
<br>
This position is ideal for individuals interested in gaining extensive research experience before pursuing graduate, medical, or professional school, or for candidates seeking a career in biomedical research. Outstanding candidates will have opportunities to co-author peer-reviewed publications and present research at regional and national scientific meetings.<br>
<br>
<b>Primary Responsibilities</b><br>
The Research Assistant will:<br>
<ul><li>Manage and maintain mouse colonies, including colony organization, record keeping, and health monitoring</li><li>Establish breeding schemes and genotyping workflows to generate experimental mouse cohorts</li><li>Assist with and perform in vivo studies, including animal handling, injections, metabolic phenotyping, glucose and insulin tolerance tests, blood and tissue collection, and other physiological assessments (training provided as needed)</li><li>Perform pancreatic islet isolations from mice (training provided as needed)</li><li>Perform molecular biology techniques including DNA/RNA extraction, PCR, qPCR, cloning, and genotyping</li><li>Conduct biochemical assays including Western blotting, ELISA, insulin secretion assays, and enzyme activity measurements</li><li>Prepare laboratory reagents and solutions, maintain laboratory equipment, manage inventory, and ensure compliance with laboratory safety procedures</li><li>Organize, analyze, and maintain accurate records of experimental data using electronic laboratory notebooks</li><li>Participate in laboratory meetings and contribute to manuscript preparation and grant applications as appropriate</li></ul><br>
<b>
Research Areas</b><br>
Projects in the laboratory focus on:<br>
<ul><li>Pancreatic islet biology and &beta;-cell physiology</li><li>Mitochondrial dynamics, cellular metabolism and bioenergetics</li><li>Aging and age-associated metabolic diseases</li><li>Translational studies using mouse and human &beta;-cell models</li></ul><br>
<b>
Training Opportunities</b><br>
The Research Assistant will receive training in modern techniques including:<br>
<ul><li>Pancreatic islet isolation and functional assays</li><li>Live-cell and super-resolution confocal imaging</li><li>Metabolic phenotyping</li><li>Molecular and cellular biology</li><li>Experimental design and statistical analysis</li><li>Scientific writing and presentation skills</li></ul><br>
<b>
Required Qualifications</b>
</div><ul><li>Bachelor&rsquo;s degree in Biology, Biochemistry, Molecular Biology, Biomedical Sciences, or a closely related field</li><li>Strong organizational and communication skills</li><li>Ability to work both independently and collaboratively</li><li>Excellent attention to detail and commitment to maintaining accurate research records; Willingness to learn new laboratory techniques</li></ul><br>
<div>
<b>Preferred Qualifications</b><br>
Experience with one or more of the following is desirable but not required:<br>
<ul><li>Experience working with laboratory mice, including animal handling and husbandry</li><li>Experience managing transgenic or knockout mouse colonies, including breeding strategies and colony record keeping</li><li>Familiarity with mouse genotyping techniques, including DNA extraction and PCR</li><li>Experience with in vivo procedures such as injections, blood collection, metabolic phenotyping, or tissue harvesting</li><li>Experience with pancreatic islet isolation or other tissue dissection techniques</li><li>Experience with mammalian cell culture and molecular biology techniques, including PCR, qPCR, Western blotting, or cloning</li><li>Familiarity with immunofluorescence microscopy or confocal microscopy</li></ul></div>
Location MURC - Marshall University Research Corporation Salary Range Salary will be commensurate with experience and qualifications.
<div><div>Required Qualifications
</div><p></p><div><div><div><div><b>Education</b></div>
<div>Bachelor&rsquo;s degree in Biology, Biochemistry, Molecular Biology, Biomedical Sciences, or a closely related field</div>
</div><br>
<div><div><b>Experience</b></div>
<div><ul><li>Strong organizational and communication skills</li><li>Ability to work both independently and collaboratively</li><li>Excellent attention to detail and commitment to maintaining accurate research records; Willingness to learn new laboratory techniques</li></ul><br>
</div>
</div><br>
</div></div></div><div><div>Preferred Qualifications
</div><p></p><div><div><div><div><b>Education</b></div>
</div><br>
<div></div><div><div><b>Experience</b></div>
<div>Experience with one or more of the following is desirable but not required:<br>
<ul><li>Experience working with laboratory mice, including animal handling and husbandry</li><li>Experience managing transgenic or knockout mouse colonies, including breeding strategies and colony record keeping</li><li>Familiarity with mouse genotyping techniques, including DNA extraction and PCR</li><li>Experience with in vivo procedures such as injections, blood collection, metabolic phenotyping, or tissue harvesting</li><li>Experience with pancreatic islet isolation or other tissue dissection techniques</li><li>Experience with mammalian cell culture and molecular biology techniques, including PCR, qPCR, Western blotting, or cloning</li><li>Familiarity with immunofluorescence microscopy or confocal microscopy</li></ul></div>
</div><br>
</div></div></div><div>Posting Detail Information
</div><p></p>Posting Number MR0887 Open Date 07/30/2026 Close Date Open Until Filled Yes Special Instructions Summary</div>

Stevens Institute of Technology

<div><p><b>Job Description</b></p><h1 class="jobSectionHeader"><b>
The Department of Mechanical Engineering in the Charles V. Schaefer, Jr. School of Engineering and Science at Stevens Institute of Technology is seeking a highly motivated Part-Time Research Assistant to support ongoing computational fluid dynamics (CFD) and aerospace engineering research projects.</b></h1><h1 class="jobSectionHeader"><b>
Essential Responsibilities</b></h1><ul><li><h1 class="jobSectionHeader"><b>
Perform and analyze Computational Fluid Dynamics (CFD) and Direct Simulation Monte Carlo (DSMC) simulations related to parachute permeability modeling.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Conduct CFD simulations using commercial software to evaluate high-Reynolds-number incompressible flows involving complex geometries.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Process, organize, and analyze simulation and experimental data to support ongoing research objectives.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Assist in the interpretation and presentation of research findings.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Contribute to the preparation, editing, and submission of peer-reviewed journal articles, conference papers, and technical reports.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Maintain accurate documentation of research methods, simulation parameters, and results.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Collaborate with faculty members, graduate researchers, and project team members to achieve research milestones.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Perform other research-related duties as assigned.</b></h1></li></ul><h1 class="jobSectionHeader"><b>
Required Qualifications</b></h1><ul><li><h1 class="jobSectionHeader"><b>
PhD with experience in CFD and DSMC simulations.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Excellent written and verbal communication skills, with the ability to contribute to technical reports and scholarly publications.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Ability to work independently and collaboratively in a research environment.</b></h1></li><li><h1 class="jobSectionHeader"><b>
Previous experience supporting academic or sponsored research projects.</b></h1></li></ul><p></p><p><b>
Department</b></p>
Mechanical Engineering
<p><b>Compensation Range</b></p>
In compliance with the New Jersey Wage Transparency Act, the hourly base range for this position is $25.00 - $30.00. This range represents the University&rsquo;s good faith estimate of possible compensation at the time of posting. Stevens Institute of Technology determines compensation based on factors including the position&rsquo;s scope and responsibilities, the candidate&rsquo;s experience, education, skills, internal equity, market data, and organizational considerations. The final salary will be set considering departmental budget, qualifications, and relevant credentials. This pay range represents base pay only and excludes additional forms of compensation, such as incentives, stipends, or other applicable pay components. For a full overview of our benefits offerings, please refer to the Stevens Institute of Technology Benefits Guidebook, available at:<p>
Benefits Guidebook</p>
<div><p><b>General Submission Guidelines:</b></p></div><div><p>
Please submit an online application to be considered a candidate for any job at Stevens. Please attach a cover letter and resume with each application. Other requirements for consideration may depend on the job.</p></div><p></p><div><p><b>
Still Have Questions?</b></p></div><div><p>
If you have any questions regarding your application, please contact Jobs@Stevens.edu.</p></div><p></p><p><b>
EEO Statement:</b></p><p></p><p>
Stevens Institute of Technology is an Equal Opportunity Employer. Accordingly, Stevens adheres to an employment policy that prohibits discriminatory practices or harassment against candidates or employees based on legally impermissible factor(s) including, but not necessarily limited to, race, color, religion, creed, sex, national origin, nationality, citizenship status, age, ancestry, marital or domestic partnership or civil union status, familial status, affectional or sexual orientation, gender identity or expression, atypical cellular or blood trait, genetic information, pregnancy or pregnancy-related medical conditions, disability, or any protected military or veteran status.</p><p></p><p>
Stevens is building a diverse faculty, staff, and student body and strongly encourages applications from people of all backgrounds. Stevens is a federal contractor under the Vietnam Era Veterans' Readjustment Assistance Act (VEVRAA) and the Rehabilitation Act of 1973, as well as other federal statutes. Stevens seeks candidates who will contribute to a welcoming and inclusive environment for all students, faculty and staff.</p><p></p><div><p><b>
Jeanne Clery Disclosure:</b></p></div><div><p>
In accordance with the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act (Clery Act), the Department of Public Safety is required to publish an annual security report which includes statistics mandated by the Clery Act. Click here for a copy of this report.</p></div></div><p></p>

University of Texas Health Science Center at San Antonio

Under general supervision, provides routine technical assistance in performing assigned and delegated tasks in support of research projects. Responsibilities include assisting or conducting a variety of scientific experiments and research projects of limited complexity, collecting, evaluating and interpreting data for clinical and diagnostic research.
<br><div><ul><li>Attention to detail by achieving thoroughness and accuracy when accomplishing a task through concern for all the areas involved.
</li><li>Ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner.
</li><li>Ability to monitor important and complex projects concurrently within a research environment or laboratory schedule.
</li><li>Ability to effectively communicate orally and in writing, to include writing and preparing memorandums, letters, and other official correspondence.
</li><li>Knowledge of Microsoft Word, Excel, PowerPoint, and Lotus Notes/other e-mail software.
</li></ul><p>Education
</p><ul><li>Bachelor's Degree in a basic science is required.</li></ul></div>
<br><div><ul><li>Provides routine technical assistance in performing assigned and delegated tasks in support of research projects.
</li><li>Performs assigned clerical and technical duties in a research or clinical lab setting.
</li><li>Assists investigator or higher level technician with research studies, experiments and assays including collection of data, preparation of solutions and set-up and maintenance of equipment.
</li><li>Performs routine tests with direction from supervisor, manager or higher level technician.
</li><li>Assists in conducting a variety of scientific experiments and research projects of limited complexity, collecting, evaluating, and interpreting data.
</li><li>Carries out general laboratory maintenance.
</li><li>Performs all other duties as assigned.</li></ul></div>

Spring Clinical Research

<p><b>Job Description:</b></p><p>We are seeking a motivated and detail-oriented Clinical Research Assistant to join our dynamic research team. The successful candidate will play a pivotal role in supporting clinical trials and research studies aimed at advancing medical knowledge and improving patient care. The Clinical Research Assistant will work closely with the research team, study participants, and healthcare professionals to ensure the smooth and ethical execution of research projects.</p><p><b>Key Responsibilities:</b></p><p><b>Participant Recruitment and Screening:</b>Identify and recruit eligible study participants according to study criteria.<br/>Screen potential participants to ensure their suitability for the research.<br/><b>Data Collection and Documentation:</b>Assist in the collection of clinical data, including medical histories, laboratory results, and vital signs.<br/>Maintain accurate and organized records of all research-related activities.<br/>Ensure data integrity and compliance with study protocols.<br/><b>Informed Consent Process:</b>Explain the research study to participants and obtain informed consent.<br/>Maintain documentation of informed consent processes.</p><p><b>Clinical Procedures: </b>Assist with clinical procedures, including administering medications, medical tests, and assessments as per the study protocol.<br/>Ensure adherence to ethical and safety standards.</p><p><b>Data Management:</b>Enter, manage, and analyze research data using electronic databases and software.<br/>Generate reports and assist in data interpretation.</p><p><b>Regulatory Compliance:</b>Ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines.<br/>Assist in preparing and submitting regulatory documents as needed.</p><p><b>Study Coordination:</b>Collaborate with principal investigators, physicians, nurses, and other healthcare professionals involved in the research.<br/>Coordinate study-related activities and scheduling.</p><p><b>Participant Follow-up:</b>Maintain regular contact with study participants to track their progress and ensure retention in the study.</p><p><b>Quality Assurance:</b>Assist in monitoring and auditing study sites to ensure protocol adherence and data quality.</p><p><b>Adverse Event Reporting:</b>Promptly report adverse events and safety concerns to the appropriate regulatory bodies.</p><p>Job Type: Full-time</p><p>Pay: $12.00 - $16.00 per year</p><p>Benefits:</p><ul><li>Flexible schedule</li></ul><p>Experience:</p><ul><li>Clinical trials: 1 year (Preferred)</li><li>Research: 1 year (Preferred)</li></ul><p>Work Location: In person</p>

Clinical Research Assistant

Community Health Network

<div><div><div><div>Category</div>
<div>Administrative &amp; General Support</div>
</div><div><div>Department</div>
<div>Clinical Research Oncology</div>
</div><div><div>Schedule</div>
<div>Full-time</div>
</div><div><div>Facility</div>
<div>Cancer Center South</div>
<div><p>1440 E County Line Rd<br>
Indianapolis, IN 46227<br>
United States</p></div>
</div><div><div>Shift</div>
<div>Day Job</div>
</div><div><div>Hours</div>
<div>80 hours per pay period</div><br>
</div></div><p></p><div><div><p><b>Join our community</b><br>
Community Health Network has an excellent opportunity available within our Clinical Research Oncology Team. If you are looking for challenging work and meaningful advancement, then you should consider a career with Community.</p><p><b><br>
Where you fit in</b><br>
The <b>Clinical Research Assistant</b> will be responsible for recruiting, screening interviewing and consenting study patients to the study protocol; completes study-related documentation and data entry; and assists with administrative activities generally associated with the conduct of clinical trials and support of the department. Supports the coordinators and investigators in identifying, screening, interviewing, and consenting eligible patients for the clinical trial and completing the associated data entry and source documentation in accordance with protocol guidelines, GCP, ICH, local, state and federal standards. Maintains effective data management system to track and report patient recruitment for the clinical trials. Assists with administrative activities generally associated with the conduct of the clinical trials and support of the department as needed and as trained. Collects, processes and ships specimens per protocol and regulations as needed and as trained</p><p></p><p><b><br>
Your exceptional skills</b></p><ul><li>
Demonstrates knowledge and understanding of the patient care process</li><li>
Demonstrates compliance with hospital standards, policies and procedures</li><li>
Demonstrates effective written and oral communication skills to a varied audience</li><li>
Demonstrates ability to interact with people from diverse socioeconomic, cultural and ethnic backgrounds</li><li>
Demonstrates organizational and time management skills and must be detail oriented</li><li>
Demonstrates computer competencies in MS Word, Excel, Outlook, and EMR</li></ul><p></p><p><b><br>
Your exceptional qualifications</b></p><ul><li>
Minimum of 1-2 years of healthcare experience.</li><li>
High school diploma or equivalent required.</li><li>
Medical Assistant or Medical Office Assistant or combined equivalent experience preferred.</li></ul><p></p><p><b><br>
Your life with Community</b><br>
You work hard to provide our patients with the exceptional care, and you deserve benefits to match. Community offers a unique employment package that encompasses not only your day-to-day job, but also your career.<br>
<br>
You will have the opportunity to grow your career thanks to scholarships and tuition reimbursement from the Community Health Network Foundation and receive recognition for your achievements.<br>
<br>
Apply today for immediate consideration.</p></div>
<p><b>Why Community?
</b></p><p>At Community Health Network, we build teams that deliver exceptional care through empathy, communication and collaboration. We consider ALL an integral part of the exceptional patient experience. We PRIIDE ourselves on not having employees but Caregivers. Join our Community as we make a difference in your community.</p></div></div><p></p>

Adams Clinical

<div>
 <strong>
  Join Us in Shaping the Future of Clinical Research
  <br/>
  <br/>
 </strong>
 Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values&mdash;Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration&mdash;we create an environment where meaningful work drives meaningful change.
 <br/>
 <br/>
 At Adams Clinical, you&rsquo;ll find:
 <br/>
 <br/>
 <ul>
  <li>
   A culture of respect, transparency, and continuous improvement
  </li>
  <li>
   Opportunities for professional growth and learning
  </li>
  <li>
   A team dedicated to improving lives through innovation and integrity
   <br/>
   <br/>
  </li>
 </ul>
 If you&rsquo;re passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we&rsquo;d love to have you on our team.
 <br/>
 <br/>
 <strong>
  Overview
  <br/>
  <br/>
 </strong>
 Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions, supporting both inpatient and outpatient studies. Adams Clinical Site Network has locations in Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; and Dallas, TX.
 <br/>
 <br/>
 We are seeking entry-level applicants for the Clinical Research Assistant role at our Boston location. This role is ideal for entry-level candidates interested in learning clinical research operations, contributing to study execution, and developing foundational skills in patient interaction, data management, and regulatory compliance.
 <br/>
 <br/>
 The Clinical Research Assistant (RA) provides foundational support in the conduct of clinical trials at the site level. Working under the direct supervision of a CRC II, CRC III, or Site Manager, the RA assists with operational, administrative, and participant-facing tasks to ensure studies run smoothly and in accordance with ICH-GCP, regulatory requirements, and protocol guidelines. This role is an ideal entry point for individuals seeking to gain hands-on experience in clinical research.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Support study start-up activities, including supply inventory, document preparation, and site initiation readiness.
  </li>
  <li>
   Assist with participant screening workflows as delegated, including scheduling screening visits and collecting basic information such as demographics, medical history, and other study-relevant details to support eligibility assessment.
  </li>
  <li>
   Schedule and prepare for participant visits, including source prep, lab kits, and CRFs.
  </li>
  <li>
   Serve as a participant liaison&mdash;confirm appointments, coordinate transportation, and maintain ongoing communication.
  </li>
  <li>
   Escort and assist participants during on-site visits; perform vital signs, ECGs, and specimen collection/processing as trained.
  </li>
  <li>
   Complete accurate, ALCOA+-compliant source documentation for delegated procedures.
  </li>
  <li>
   Perform data entry into EDC systems and assist with query resolution.
  </li>
  <li>
   Maintain study binders, charts, and logs; support supply management.
  </li>
  <li>
   Ensure accurate capture and upload of paper source documents into eSource systems in accordance with site processes and regulatory requirements, supporting long-term retention and audit readiness.
  </li>
  <li>
   Obtain, track, and manage medical releases, as well as medical and pharmacy records from external providers as needed, in accordance with site SOPs and protocol requirements.
  </li>
  <li>
   Support CRCs during monitoring visits and assist with preparing documentation and materials to ensure audit and inspection readiness.
  </li>
  <li>
   Assist with investigational product (IP) accountability tasks as needed and where applicable, gaining exposure to IP handling, tracking, and documentation under the direct supervision of CRC staff, while ensuring adherence to protocol and site SOPs.
  </li>
  <li>
   Develop proficiency in site SOPs, institutional policies, and GCP requirements to build foundational knowledge in compliant research practices.
  </li>
  <li>
   Assist in collecting and entering study data into trackers, logs, and EDC systems, focusing on accurate and timely data collection.
  </li>
  <li>
   Support CRCs in maintaining accurate records and updating study metrics.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Minimum requirement of a high school diploma or GED equivalent; Bachelor&rsquo;s degree preferred.
  </li>
  <li>
   No prior clinical research experience is necessary; training will be provided. Basic understanding of clinical research principles is a plus.
  </li>
  <li>
   Strong attention to detail, organization, and communication skills.
  </li>
  <li>
   Proficiency in Microsoft Office.
  </li>
  <li>
   Willingness to perform phlebotomy and clinical procedures as trained.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Pay
 </strong>
 : $24.00 - $26.92 per hour
 <br/>
 <br/>
 <strong>
  Benefits
 </strong>
 :
 <br/>
 <br/>
 <ul>
  <li>
   401(k) matching
  </li>
  <li>
   Medical, Dental &amp;Vision insurance
  </li>
  <li>
   Employee assistance program
  </li>
  <li>
   Flexible spending account
  </li>
  <li>
   Health insurance
  </li>
  <li>
   Health savings account
  </li>
  <li>
   Life insurance
  </li>
  <li>
   Paid time off
  </li>
  <li>
   Parental leave
  </li>
  <li>
   Professional development assistance
   <br/>
   <br/>
  </li>
 </ul>
 Adams Clinical is committed to being an equal opportunity and affirmative action employer. We focus on hiring and nurturing top talent. All employment decisions, including recruitment, hiring, promotion, compensation, transfer, training, discipline, and termination, are made based on the candidate's or employee's qualifications relevant to the position. These decisions are made without regard to age, sex, sexual orientation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected status.
 <br/>
 <br/>
 In compliance with federal law, all individuals hired must, as a condition of employment, provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the required timeframe. Adams Clinical participates in E-Verify to confirm employment eligibility.
</div>


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