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Through our exclusive lease purchase program with Expediter Services, you'll discover how easy purchasing a new tractor can be for your team. We'll support you and your co-driver on your path to truck ownership while providing the resources you need to stay as busy as you choose.

<h3><strong>Now Leasing Team CDL-A Contractors</strong></h3><p/><p>Get your team into its own truck with no money down, no minimum credit requirement and flexible financing options. We'll support you and your co-driver on your path to truck ownership while providing the resources you need to stay as busy as you choose. Keep moving - and earning - together with Panther.</p><p/><p><strong>Exclusive to Teams</strong></p><p>Work for yourselves, see the country and set your own schedule. Through our exclusive lease purchase program with Expediter Services, you'll discover how easy purchasing a new tractor can be for your team. Payments are deducted from your weekly settlement for the specified term and then the tractor is yours.</p><p/><p>All drivers and vehicle owners are independent contractors.</p><p>**Truck and financing are through an independent Third Party.</p><br/><h3>Pay & Benefits</h3><ul><li>No money down</li><li>No minimum credit requirements</li><li>No balloon payment</li><li>Flexible finance options</li><li>Actual lease is through Expediter Services</li><li>Earn top pay for safe, precise, on-time delivery, and stay as busy as you want.</li><li>Set your own schedule</li><li>99% no-touch, high-value expedite freight</li><li>Weekly settlements</li><li>Access to our driver support team 24/7/365</li><li>We provide a fuel surcharge along with your standard rate per shipment</li></ul><p><br/></p><h3>Requirements</h3><ul><li>CDL-A + 6 months minimum experience*</li><li>At least 21 years of age</li><li>No DUI or drug convictions in the last 5 years</li><li>No felonies in the last 10 years</li><li>*No experience necessary for straight trucks or cargo vans</li><li>** All drivers and vehicle owners are independent contractors.</li><li>**Truck and financing are through an independent Third Party.</li></ul><br/>

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Truck Drivers - Leasing Team CDL-A Contractors

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Class A License

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Founded in 2021, SiteBridge Research is an integrated research organization, focused on building a national network of small and community medical practices to deliver world-class industry-sponsored clinical research studies on time and on budget, accelerating time to completing clinical trials, accelerating time to market and product adoption in communities that are often underrepresented and difficult to reach. The SiteBridge Network extends reach further into these communities to empower patients with some of the highest unmet needs to take part in clinical studies to improve inclusivity in clinical research and to improve overall health outcomes.

HOUR

<p/><p><strong>SiteBridge Research Inc:</strong></p><p><em>Founded in 2021, SiteBridge Research is an integrated research organization, focused on building a national network of small and community medical practices to deliver world-class industry-sponsored clinical research studies on time and on budget, accelerating time to completing clinical trials, accelerating time to market and product adoption in communities that are often underrepresented and difficult to reach. The SiteBridge Network extends reach further into these communities to empower patients with some of the highest unmet needs to take part in clinical studies to improve inclusivity in clinical research and to improve overall health outcomes.</em></p><p><strong>Job Description: Clinical Research Coordinator/Clinical Research Nurse Coordinator - Contractor</strong></p><p>The <strong>Clinical Research Coordinator</strong>/<strong>Clinical Research Nurse Coordinator (CRC/CRNC) </strong>is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI) on multiple ongoing research studies. While the Principal Investigator is ultimately responsible for the clinical trial, the CRC/CRNC is responsible for the facilitation and coordination of the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC/CRNC works collaboratively with the entire site team, Sponsors, and clinical monitors to ensure ICH/GCP compliance, site productivity, and timely completion of studies. In addition, and most importantly, this role represents our mission and vision by focusing on the trusted physician/patient partnership from start to finish for every clinical trial conducted at the site and is key in transforming clinical research for every participant. The position will be responsible for specific clinical site activities to maintain the operational excellence required of clinical sites/staff involved in clinical studies and to assure compliance with protocol-specific procedures, data acquisition, and records management. Persons in this role will report to the Head of Clinical Operations.</p><p>The position is located in Lufkin, TX and will be required to be on-site.</p><p>This is a 1099 Independent Contractor role and is full-time hours. </p><p><strong>Responsibilities</strong></p><ul><li>Ensure clinical study compliance with local and federal laws and regulations according to ICH/GCP Guidelines.</li><li>Ensure study feasibility assessments for contracted Sponsor-initiated studies.</li><li>Assist the Clinical/Site Ops leads on the set-up/start-up of research site to prepare for start-up and conduct of clinical trials.</li><li>Lead oversight of pre-study, site initiation, and close-out visits with sponsor or CRO. </li><li>Consult with Site leads, Sponsor, and CRO to determine the best recruitment practices for site and trials.</li><li>Track study activities to ensure compliance with standard operating procedures (SOPs), protocols, and all related local, state, and national regulatory and institutional policies.</li><li>Arrange screening and recruitment of potential study participants by scheduling visits to establish Informed Consent and perform intake assessments according to protocols.</li><li>Create and maintain all essential documents and records related to the study.</li><li>Acts as a point of reference for study participants by answering questions and keeping them informed on the study’s progress.</li><li>Oversee and/or manages the inventory of equipment and supplies related to the study, including documentation, reporting of issues, and ordering clinical supplies as needed.</li><li>Communicate with laboratories and clinical investigators to ensure review and reporting of lab results and other clinical testing results.</li><li>Direct the request, collection, labeling, storage, administration or shipment of interventional products.</li><li>Ensure collection of specimens, questionnaire information, and input of data and patient information into electronic clinical systems.</li><li>Monitor the enrollment status of participants at the site for each specific clinical study.</li><li>Operate as primary contact for Sponsors/CROs to schedule and coordinate site visits and answer queries.</li><li>Participate in meetings (ie., Investigator Meetings, Site Trainings) and seminars to update knowledge of clinical research and related issues.</li><li>Prepare or participate in quality assurance audits and inspections performed by Sponsors/CROs, regulatory authorities, or exclusively designated review groups.</li><li>Provide regular updates to Site Clinical Investigator(s) and Clinical/Site Ops leads on study progress related to recruitment, compliance, and other study-related matters. </li></ul><p><strong>Qualifications/Required Experience--</strong></p><ul><li>Requires Bachelor’s degree in a relevant life science discipline is preferred, RN (BSN) is preferred; certification as CCRC/CCRP is a plus.</li><li>1+ year of previous experience working in a clinical setting; years of clinical site/trials experience will determine position level.</li><li>Bilingual – Fluent in Spanish is highly preferred.</li><li>Excellent working knowledge of FDA & ICH GCP regulations and guidelines is required.</li><li>Strong preference for experience with late phase and observational clinical research.</li><li>Managing necessary clinical study and staff records related to clinical study activity which includes case report forms, drug dispensation records, etc.</li><li>Preparing advertising and other educational materials and conducting campaigns to recruit and enroll subjects.</li><li>Preparing trial-related document support such as protocol worksheets, adverse event reports, IRB documents, procedural manuals, and progress reports.</li><li>Experience identifying, reviewing, and reporting adverse events, protocol deviations, or other unanticipated problems appropriately to investigators and/or regulatory agencies.</li><li>Assessing risk factors in study protocols such as sample collection procedures, data management issues, and possible subject threats.</li><li>Clinical and laboratory skills, including the ability to perform phlebotomy and process samples are preferred.</li><li>Detail-oriented and meticulous in all aspects of work.</li><li>Strong follow-through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative.</li><li>Superior organizational and time management skills.</li><li>Capable of working independently with minimal supervision and as part of a team.</li><li>Understanding of medical terminology as well as standard clinical procedures and protocol.</li><li>Ability to lift approximately 20 pounds for a short period and capable of standing for extended periods of time.</li></ul><p><strong> Additional Qualifications</strong></p><ul><li>Strong Project Management skills including risk assessment and contingency planning</li><li>High level of collaboration, customer orientation awareness, and focus</li><li>Skilled with standard computer programs including the MS Office suite</li><li>Strong interpersonal and written and verbal communication skills </li><li>Therapeutic experience in alignment with primary protocol(s) and site practice preferred</li><li>Some travel may be required</li></ul><p><strong>Pay Range:</strong></p><p>The combined pay range for this role is $27 - $32/hour. Title and salary will be based on our assessment of skills and experience relevant to our needs for the role.</p><p><strong>Additional Information</strong></p><p><em>SiteBridge Research, Inc. is proud to be an Equal Opportunity Employer providing employees with a work environment free of discrimination and harassment. We respect and seek to empower each individual and value the diverse cultures, perspectives, skills, and experiences within our workforce. We celebrate diversity and do not discriminate based on race, religion, color, national origin, sex, sexual orientation, age, veteran status, disability status, or any other applicable characteristics protected by law. All employment decisions at SiteBridge are based on business needs, job requirements, and individual qualifications and performance.</em></p>

SiteBridge Research, Inc.

Clinical Research Nurse Coordinator - Contractor

HiringThing

Service Entrance Work: Installing or repairing electrical service entrances, including main disconnects and meter bases. Load Calculations: Performing precise load calculations to ensure electrical systems are properly designed and meet all capacity needs.

Are you a talented and reliable General electrician ready to take control of your career and maximize your earnings? Synergy Preserve LLC is actively looking for independent contractor electricians to join our growing team!<br/>If you have a strong background in electrical systems and love solving problems, this is the perfect opportunity for you. You'll work on a wide variety of projects in residential and commercial properties, enjoying excellent pay for every job you complete.<br/><br/><strong>Why You'll Love Working with Us:</strong><ul><li>We believe in supporting our independent contractors with outstanding benefits:</li><li>Flexible Hours: You're in charge! Manage your own schedule to fit your lifestyle.</li><li>Weekly Pay: Get paid consistently every Monday – reliable income you can count on.</li><li>Gas Disbursement: We help cover your costs with travel expense coverage.</li><li>High Earning Potential: Our contractors typically earn around $2,000 weekly!</li></ul><br/><strong>Your Responsibilities Will Include:</strong><ul><li>System Installation & Repair: Installing, maintaining, and repairing electrical systems for both homes and businesses.</li><li>Panel Upgrades: Installing and upgrading electrical panels to meet current code requirements and boost power capacity.</li><li>Load Calculations: Performing precise load calculations to ensure electrical systems are properly designed and meet all capacity needs.</li><li>Service Entrance Work: Installing or repairing electrical service entrances, including main disconnects and meter bases.</li><li>New Construction Wiring: Wiring new homes, buildings, and large commercial projects to code.</li><li>Grounding & Bonding: Performing grounding and bonding of electrical systems to prevent electrical shock hazards.</li><li>Troubleshooting & Repair: Expertly troubleshooting and repairing faulty circuit breakers, fuses, and wiring issues.</li><li>Lighting Control Systems: Installing, repairing, and maintaining lighting control systems (e.g., dimmers, occupancy sensors).</li><li>Electrical Distribution: Installing and maintaining electrical distribution systems, including transformers and distribution boards.</li><li>Code Compliance: Conducting thorough electrical inspections and ensuring all work rigorously complies with the National Electrical Code (NEC).</li><li>Workplace Safety: Maintaining a clean, safe, and organized work environment at all times.</li></ul><strong>Requirements:</strong><ul><li>A valid driver’s license and reliable transportation.</li><li>Necessary tools for comprehensive electrical work.</li><li>Proven experience and proper certifications as a licensed electrician.</li><li>A proactive attitude and the ability to work independently while delivering top-notch service.</li></ul><br/>Ready for flexible hours, great pay, and the freedom to manage your schedule while working on cool projects?<br/>Apply today to join Synergy Preserve LLC and start earning big!<p>Powered by JazzHR</p>

Synergy Preserve

General Electrician

partner JazzHR

OTHER

ThirdChannel equips passionate brand reps with powerful retail technology, creating seamless connections between people, data, and performance in-store and online. All representatives will receive a paid program-specific certification before visits, ensuring you are fully prepared and set up for success.

<p/><h1><strong>Brand Representative – Premium Optical</strong></h1><h3>Independent Contractor | Flexible Hours | Competitive Pay + Travel Incentives</h3><h2><strong>About Prada & Luxottica</strong></h2><h3>Prada and Luxottica are two of the most recognized names in global luxury. Together, they represent a heritage of innovation, design, and craftsmanship in eyewear. This project offers a rare opportunity to partner with both brands and help ensure their collections stand out at retail.</h3><h2><strong>The Opportunity</strong></h2><h3>We're looking for Brand Representatives to support an exciting new initiative in select markets. This is a supplemental income opportunity as an independent contractor (1099).</h3><h3>Your market may include multiple store locations, each with a set visit schedule. Unlike merchandising-heavy roles, this project is focused on observing and supporting the in-store brand experience, ensuring products reflect the highest standards of presentation and excellence.</h3><h2><strong>What You'll Do</strong></h2><ul><li><h3>Coordinate visit with assigned location/locations</h3></li><li><h3>Visit retail locations starting late October</h3></li><li><h3>Observe the store environment and product presentation</h3></li><li><h3>Follow provided program guidelines and submit reporting through digital tools</h3></li><li><h3>Represent Prada and Luxottica with professionalism, attention to detail, and confidence<br/><br/></h3></li></ul><h2><strong>What We're Looking For</strong></h2><ul><li><h3>Passion for premium brands, luxury retail, or iconic brands like Prada and Luxottica</h3></li><li><h3>Previous retail, customer service, or brand representation experience preferred</h3></li><li><h3>Strong communication and observation skills</h3></li><li><h3>Professional, reliable, and detail-oriented</h3></li><li><h3>Access to reliable transportation<br/><br/></h3></li></ul><h2><strong>Training & Support</strong></h2><h3>All representatives will receive a paid program-specific certification before visits, ensuring you are fully prepared and set up for success.</h3><h2>Why You'll Love It</h2><ul><li><h3>Compensation: Competitive pay for each completed 2-hour visit</h3></li><li><h3>Travel Incentives: Additional pay based on approximate distance </h3></li><li><h3>Flexibility: Create your own schedule in partnership with store management</h3></li><li><h3>Experience: Build brand representation, retail, and customer service expertise<br/><br/></h3></li></ul><h3></h3><h2><strong>Details</strong></h2><ul><li><h3>Type: Independent contractor (1099)</h3></li><li><h3>Commitment: 2 hours per store visit</h3></li><li><h3>Start: Late October or early-mid November, once onboarding certification is complete</h3></li><li><h3>Requirements: Smart device with internet access (iOS 16.0+ or Android 13.0+)</h3></li></ul><h2>Powered by ThirdChannel</h2><h3>ThirdChannel equips passionate brand reps with powerful retail technology, creating seamless connections between people, data, and performance in-store and online.</h3><p>#indprada1</p>

ThirdChannel

Premium Eyewear Assessment Rep

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Your one-stop-shop for Contractor jobs in Lufkin, TX. Apply to exciting opportunities today on Monster.

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SiteBridge Research, Inc.

Synergy Preserve

ThirdChannel

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