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With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. The Clinical Research Assistantis an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator.

HOUR

<div class="content-intro">About Care AccessCare Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.To learn more about Care Access, visit <a href="http://www.careaccess.com/" rel="nofollow">www.CareAccess.com</a>.</div><h3>How This Role Makes a Difference</h3>The Clinical Research Assistantis an entry level clinical position and is designed to fully integrate the individual in the Care Access Research process while learning the skills necessary to be a Clinical Research Coordinator. This position has potential growth and advancement within the Care Access Research organization. <div><h3>How You'll Make An Impact</h3><ul><li>Ability to understand and follow institutional SOPs   </li><li>Participate in recruitment and pre-screening events (may be at another location) </li><li>Assist with preparation of outreach materials  </li><li>Identify potential participants by reviewing medical records, study charts and subject database   </li><li>Assist with recruitment of new participants by conducting phone screenings  </li><li>Request medical records of potential and current research participants   </li><li>Schedule visits with participants, contact with reminders   </li><li>Obtain informed consent per Care Access Research SOP, under the direction of the CRC </li><li>Complete visit procedures as required by protocol, under the direction of the CRC </li><li>Collect, process and ship specimens as directed by protocol, under the direction of the CRC </li><li>Record data legibly and enter in real time on paper or e-source documents  </li><li>Request study participant payments </li><li>Update all applicable internal trackers and online recruitment systems </li><li>Assist with query resolution   </li><li>Assist with administrative tasks such as copying, scanning, filing, mailing, emailing, etc.   </li><li>Assist with maintaining all site logs  </li><li>Assist with inventory and ordering equipment and supplies  </li><li>Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials. </li><li>Maintain effective relationships with study participants and other care Access Research personnel. </li><li>Interact in a positive, professional manner with patients/participants, sponsor representatives, Investigators and Care Access Research personnel and management. </li><li>Communicate clearly verbally and in writing. </li><li>Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. </li></ul><h3>The Expertise Required</h3><div><ul><li>Bilingual in Spanish required</li><li>Ability and willingness to work independently with minimal supervision   </li><li>Ability to learn to work in a fast-paced environment   </li><li>Excellent communication skills and a high degree of professionalism with all types of people </li><li>Excellent organizational skills with strong attention to detail   </li><li>A working knowledge of medical and research terminology   </li><li>A working knowledge of federal regulations, Good Clinical Practices (GCP)   </li><li>Critical thinker and problem solver   </li><li>Friendly, outgoing personality with the ability to maintain a positive attitude under pressure   </li><li>Contribute to team and site goals   </li><li>Proficiency in Microsoft Office Suite   </li><li>High level of self-motivation and energy   </li><li>An optimistic, "can do" attitude   </li></ul></div><div><div class="text-body text-muted">Certifications/Licenses, Education, and Experience:</div></div><div><ul><li>A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist.   </li><li>Phlebotomy Experience and Proficiency Required </li><li>Some Clinical Research experience preferred   </li><li>California based roles require National phlebotomy certification by an organization approved by the California Department of Public Health </li><li>Louisiana based roles require National phlebotomy certification by an organization approved by the Louisiana State Board of Medical Examiners </li><li>Washington based roles require National phlebotomy certification by an organization approved by the Washington State Department of Health </li><li>Nevada based roles require Laboratory Assistant certification by the Division of Public and Behavioral Health </li></ul></div><h3>How We Work Together</h3><ul><li>Location: This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role. Overnight travel will be minimal (<10%). </li><li>Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.</li></ul>The expected salary range for this role is $19.00 - $33.00 USD per hour for full time team members.<div class="c-virtual_list__item" id="message-list_bottomSpacer"></div><h3>Benefits & Perks (US Full Time Employees)</h3><ul><li>Paid Time Off (PTO) and Company Paid Holidays</li><li>100% Employer paid medical, dental, and vision insurance plan options</li><li>Health Savings Account and Flexible Spending Accounts</li><li>Bi-weekly HSA employer contribution</li><li>Company paid Short-Term Disability and Long-Term Disability</li><li>401(k) Retirement Plan, with Company Match </li></ul></div><div class="content-conclusion">Diversity & InclusionWe work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.Care Access is unable to sponsor work visas at this time.If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.comMandatory Employer Disclosures: Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction. Notice to Connecticut applicants: Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment. Notice to Arizona, Georgia, Indiana, and North Dakota applicants: Care Access complies with applicable laws prohibiting smoking in and around places of employment. Notice to Massachusetts applicants: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Notice to Rhode Island applicants: Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws. Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. </div>

Care Access

Clinical Research Assistant (Must be Bilingual)

Administrative Skills

Behavioral Health

Candidate Screening

Clinical Research

Clinical Trial

Communication Skills

Community Health

Community Support

Dental Insurance

Detail Oriented

EMT-Paramedics

FDA Requirements

Federal Laws and Regulations

GCP (Good Clinical Practices)

Health Department

Healthcare

ICH Regulations

Informed Consent

Keyboards

Licensed Practical Nurse/Licensed Vocational Nurse

Maintain Compliance

Medical Assistance

Medical Records

Medical Research

Medicine

Microsoft Office

Multilingual

Order Supplies

Organizational Skills

People Management

Phlebotomy

Physical Demands

Problem Solving Skills

Public Health

Regulatory Compliance

Sample/Specimen Processing

Spanish Language

Standard Operating Procedures (SOP)

Team Building

Team Lead/Manager

Travel Planning

Vision Plan

Willing to Travel

eSourcing

GreenHouseAPI

OTHER

Using this knowledge, incumbent will complete evaluation and adjustments in an accurate and timely manner; the goal is to have the initial evaluation and approval or rejection with adjustment completed and communication with production team within 30 minutes. Interact with salesforce, R & D, Supply Chain, and Leadership teams to address any problems and performance testing and manufacturing of commercial products.

Job Title: Quality Technician (Manufacturing) (OVERNIGHT SHIFT) Job #: 2026-17686Schedule: 11:00pm to 7:30am Monday thru FridayLocation: Houston, TXIndustry: Manufacturing (Paint, Coatings, Chemicals)Salary: $19 to $28 Hourly (Depending Upon Experience)Background: Must be able to pass a Background Check and Drug Test (No Exceptions)Education: High School Diploma (Required)<a href="https://www.axalta.com/corporate/en_US.html" rel="nofollow noopener noreferrer" target="_blank">https://www.axalta.com/corporate/en_US.html</a> (Company Website Link)Overview:At Axalta, the strength of our company lies in our people, and our legacy is built on more than 150 years in the coatings industry. With over 12,000 employees globally and $4.5B annual revenue, singular focus on providing brilliant coatings sets us apart. Axalta Coating Systems is the only leading global coatings company dedicated solely to the development, manufacture and sale of liquid and powder coatings. We serve customers in the automotive, transportation, general industrial and architectural and decorative sectors. Our innovative products and services include paint, color matching tools, application technologies and customer training and business management systems.Position Description:This position is responsible for developing an in-depth knowledge of Axalta Powder Coatings products through lab work and evaluation as required. Using this knowledge, incumbent will complete evaluation and adjustments in an accurate and timely manner; the goal is to have the initial evaluation and approval or rejection with adjustment completed and communication with production team within 30 minutes. Associate must show the capability of making good decisions and getting others involved when needed. Responsibilities:<ul><li>Interact with salesforce, R & D, Supply Chain, and Leadership teams to address any problems and performance testing and manufacturing of commercial products</li><li>Review, research and complete tests in support of product manufacture</li><li>Provide clear and accurate documentation and direction of all decisions to meet requirements</li><li>Champion system processes: SAP, Datacolor, Document Control, Filing, and Communication.</li><li>Utilize product outcomes to determine product adjustment for future manufacture</li><li>Audit and follow up on the effectiveness of the corrective and preventive actions</li><li>Maintain any related Quality System Documents (ISO 9001 /TS 16949)</li><li>Perform all lab duties including production of lab size samples, application and evaluation of finished products and daily clean up and maintenance of lab area and equipment</li><li>Communicate effectively between Axalta teams (sales, QC, R&D, site, Supply Chain, etc.)</li><li>Travel when necessary to develop skills/training purposes</li><li>Other duties to support site quality initiatives</li><li>Perform all tasks in a safe and reliable manner</li><li>Navigate and perform activity SAP Datacolor Database</li><li>Application of Powder coatings to complete all testing</li><li>Follow Hilliard EHS&S policy requirements; Wear proper PPE, ex safety glass, static dissipating steel toed shoes, gloves, respirator, etc. in the required areas</li><li>Maintain all logs (Adjustment History, Calibration verification, Records on panels, Finished Goods Log Sheet, Batch tickets and all required signatures on them.</li></ul>Qualifications: Incumbent must be able to perform each duty satisfactorily and in a safe and manner. The items listed below represent the knowledge, skills, and experience required.<ul><li>High school diploma required</li><li>Working experience in a related position is highly preferred.</li><li>To perform this job successfully, an individual should have knowledge of Microsoft Word, Excel, Windows.</li><li>Ability to navigate and data entry in SAP system</li><li>Ability to follow directions independently with little or no supervision</li><li>Good attendance and punctuality</li><li>Above average logic, reasoning, and problem-solving skills</li><li>Basic math, computer and reading and comprehension skills</li><li>Good time management and ability to deliver results when needed </li><li>Strong work ethic and personal motivation; a self-starter</li><li>Strong verbal and written communication skills</li><li>Good hands-on, mechanical aptitude</li><li>Detail oriented with an aptitude for inspection</li></ul>

Axalta Coating Systems

Quality Technician (Manufacturing) (OVERNIGHT SHIFT) (11pm to 7:30am)

Architectural Services

Background Investigation

Business Solutions

Corrective Action

Customer Training

Data Entry

Document Control

Documentation

High School Diploma

ISO 9001

Industrial Coating

Laboratory

Laboratory Analysis

Laboratory Equipment

Leadership

Manufacturing

Mathematics

Microsoft Excel

Microsoft Windows Operating System

Microsoft Word

Painting (Facilities and Maintenance)

Performance Testing

Powder Coating

Presentation/Verbal Skills

Product Support

Product Testing

Quality Assurance

Quality Control

Quality Management

Research & Development (R&D)

Safety/Work Safety

Sales

Salesforce.com

Specimens/Samples

Supply Chain

TS 16949

Testing

Time Management

Writing Skills

Broadbean

FULL_TIME

YEAR

Serving the aerospace, healthcare, education, homeland security and energy industries, GB Tech delivers scalable solutions that help companies, technology partners and government agencies quickly identify and effectively respond to rapid change in today’s most dynamic markets. Stock Clerks will be proficient with the Single Application Resource for Aerospace Hardware (SARAH) database for entering, updating, and extracting data associated with the issue and receipt of hardware, materials, and equipment.

GB Tech provides managed IT, software testing and logistics services for solutions that demand mission-critical precision and scalability. Serving the aerospace, healthcare, education, homeland security and energy industries, GB Tech delivers scalable solutions that help companies, technology partners and government agencies quickly identify and effectively respond to rapid change in today’s most dynamic markets. GB Tech provides an outstanding benefits package to all full-time regular employees, including medical, dental, vision, short-term and long-term disability, life insurance, paid time-off, tuition reimbursement, company matching 401(k)!GB Tech, Inc. has an immediate need for a Full Time Bond Room Stock ClerkJob Responsibilities: Storekeeping services for the EVA-EMU Bond Room located at the Sonny Carter Neutral Buoyancy Laboratory Facility (NBL).  Provide safe, rapid and accurate issuing of identified components required for NBL training activities scheduled daily.  Issued components will be returned to stock in a timely manner, and fully documented at the completion of the training activity.  All transactions will be organized using a systematic process to assure that all documents have been completed, accounted, and securely maintained.  Stock Clerks will be proficient with the Single Application  Resource for Aerospace Hardware (SARAH) database for entering, updating, and extracting data associated with the issue and receipt of hardware, materials, and equipment.  Transactions will be maintained on a current basis, and a daily audit and verification will be performed toconfirm all transactions are posted.  Stock Clerk will conduct perpetual inventory activities including hands-on physical verification, cycle counts, inventory reconciliation, and shift-to-shift verification of transactions.  REQUIRED SKILLS:Strong Communicator, Successful in Team Environment, Computer Aptitude, Basic Accounting, Disciplined in Working to Exact & Defined Procedures, Record Keeping, Ability to Flex hours and Work Overtime.EOE/ADA  Powered by JazzHR

Overnight Research Jobs in Houston, TX

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Overnight Research Jobs in Houston, TX

Clinical Research Assistant (Must be Bilingual) Care Access

Quality Technician (Manufacturing) (OVERNIGHT SHIFT) (11pm to 7:30am) Axalta Coating Systems

Bond Room Stock Clerk GB Tech, Inc

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