Senior Medical Writer, Global Regulatory Communication - Job ID: 1693

Clinical Research Principal Investigator (MD or DO Only – All Specialties Welcome) Remote Matching · Contract · Dallas, Texas, United States   IMPORTANT: CLICK HERE for FREE REGISTRATION to our ClinPI Clinical Trials Board Are you a hospitalist, private practice physician, or existing principal investigator looking to supplement your income and contribute to medical innovation—without adding administrative burden or sacrificing your clinical autonomy? Join Clinitiative Health Research's ClinPI™ Program, a nationwide initiative that matches board-certified physicians with local, flexible clinical trial opportunities based on your specialty and availability. No research experience required. We provide full training, mentorship, and support. Opportunity Highlights Flexible schedule: Set your own hours (typically 5–10+ hours/week) Local studies only: Opportunities are based in the city where you currently live or practice Minimal administrative work: Site staff manages study paperwork Standard-of-care clinical work: No procedures outside typical patient care within the protocol Malpractice covered: No additional insurance needed—you are indemnified by the sponsor Study durations: Trials typically last 3 to 12 months Tailored matching: You will be matched with trials aligned with your specialty and clinical interests The Process Apply online Complete your physician career profile (medical background, specialty, clinical preferences) Upon approval, you are registered into the ClinPI™ Program You will receive portal access where you can: Register for our clinical research training course View available trials in your area Apply to studies that fit your interests, specialty, and time availability Once matched, we will connect you with the participating research site for onboarding and trial initiation Role Responsibilities Serve as a Principal Investigator (PI) or Sub-Investigator on studies Conduct study visits aligned with standard-of-care clinical duties Ensure compliance with protocol and regulatory requirements Collaborate with study coordinators and site teams Maintain GCP standards (certification provided if not already completed) Who This Is For Hospitalists, private practice physicians, or locum providers seeking flexible supplemental income Clinicians curious about research but unsure where to start Physicians wanting to advance medicine while maintaining their clinical independence Join ClinPI™ to explore the clinical research world without making a career shift. This is not a job posting for one role—it is a gateway to a steady stream of vetted, compensated trial opportunities, with no cost to join. Apply now to unlock your earning potential in research and take the first step toward becoming a Principal Investigator.   Requirements M.D., D.O, or equivalent doctoral-level degree Active, unrestricted medical license in your state Board certification in your specialty Willingness to see patients at a designated research site No prior research experience required—training and mentorship provided IMPORTANT: CLICK HERE for FREE REGISTRATION to our ClinPI Clinical Trials Board

Sitter needed Monday through Friday 6 a.m.- 4:45 p.m. Must be able to be on time and work these hours. Must enjoy walking outdoors. Must have reliable transportation and a valid drivers license. Nursing home experience strongly preferred

The Data Insight Analyst is responsible for acquiring, managing and analyzing data that will be presented to internal teams, clients and partners. The Data Analyst leads the onboarding of electronic data trading partners and is responsible for the success of trading partner implementations. The Data Quality Analyst is responsible for monitoring client data submissions and communicating with them in the resolution of data quality issues. Requirements Developing reports and analytics using data from data warehouse and Salesforce using Excel, SQL, Tableau, and other reporting/analytics tools. Provide consultative insights: Analyze data to identify patterns and trends over time. Compare data from different categories to identify relationships or correlations. Applying statistical analysis to identify patterns and relationships in the data. Provide context and explanations for the data by using visualizations and narrative descriptions. Identify outliers or anomalies in the data and investigate their causes. Review and QA data/report before it is provided to the client (internal/external). Communicates directly with customer on data needs and key deadlines. Researches and identifies data quality issues. Manage ongoing, incoming partner requests and questions regarding data specifications. Configures mapping tools to support translation from source data to desired format. Includes testing of tool and providing clear documentation to internal resources and customer. Act as resident expert for data requirements/specifications internally and for the client as needed. Remain informed and up to speed with ongoing changes and evolution of assigned program data specs. Lead client/partner web-based trainings regarding data specifications and requirements. Qualifications: Self-starter, an individual who is not fully dependent on direction to fulfill the functions of the role. Thrives in an entrepreneurial-like environment. Experience with Tableau and Salesforce reporting preferred. Experience with healthcare and/or pharmacy data preferred. Experience with Microsoft Excel and SQL is a must. Previous client-facing experience is a must. Must be extremely responsive, able to work under pressure in crisis with a strong sense of urgency. Benefits Supportive, progressive, fast-paced environment Competitive pay structure Matching 401(k) with immediate vesting Medical, dental, vision, life, & short-term disability insurance AssistRx, Inc. is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, religion, color, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, family medical history or genetic information, political affiliation, military service, or other non-merit based factors, or any other protected categories protected by federal, state, or local laws. All offers of employment with AssistRx are conditional based on the successful completion of a pre-employment background check. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. Sponsorship and/or work authorization is not available for this position. AssistRx does not accept unsolicited resumes from search firms or any other vendor services. Any unsolicited resumes will be considered property of AssistRx and no fee will be paid in the event of a hire

We need a live in caregiver for a homebound patient. Person with little experience is welcomed to apply but must be willing to help. Serious applicants please reply with your phone number so we can contact you.

The Mission At RDI, we are building something most of the world thinks is impossible: A clinical trial engine that actually works — for the sponsors who need results, for the labs that generate data, and for the patients waiting on therapies. We sit at the intersection of clinical trials, laboratory operations, and highly specialized data systems — building trials that run faster, cleaner, and with fewer unforced errors, by closing the gaps that usually sink timelines. This is a company designed to build better systems for how trials are actually run. The Role We’re hiring a Clinical Operations Lead — someone who can both do the work and build the system. You will own trial execution — start to finish — while designing the systems that allow us to scale. You will mentor junior operators, work directly with sponsors, and stand between us and the thousand small failures that collapse studies. There is no giant department here. No safety net of redundant processes. If something breaks, you will see it. You will fix it. You will prevent it from happening again. You will work directly with the CEO and a highly driven cross-functional team. We are not looking for someone who wants a quiet management role. We are looking for a builder, operator, and coach who wants to create something that outlasts them. What You Will Actually Do Design and execute full clinical trial operations — protocol to closeout. Build the operational playbooks, systems, and SOPs we need to scale. Manage vendors, sites, CROs, and labs directly. Oversee enrollment, timelines, budgets, compliance, and data integrity. Train and mentor our junior team as they develop into full PMs. Sit across sponsors, labs, and internal teams to keep every trial on track. Solve problems that don’t yet have names. Build systems that make the next trial easier than the last. Who You Are You’ve run full clinical trials, from startup through closeout, with real accountability for timelines, vendors, and data. You’ve worked on the sponsor side, where the real accountability lives. You’ve built processes before — not just followed them. You are deeply familiar with GCP, ICH, IRB, site management, and clinical regulations. You can see around corners, spot operational risks early, and course-correct without drama. You love developing people and building team capacity. You write clearly, speak directly, and own your work. You are fully accountable — when things go wrong, you don’t point fingers; you fix them. Who You Are Not You’re not looking to “oversee” a team that does the work. You’re not afraid of ambiguity. You don’t need someone to hand you a 400-page SOP binder to get started. You don’t hide behind process when decisions need to be made. The Conditions Location: Los Angeles preferred. Remote considered for exceptional candidates. Travel: Occasional (site visits, internal meetings, vendor oversight)

Delivery Driver for dental laboratory (Stuart-Port Saint Lucie) compensation: $14\h employment type: full-time experience level: entry level job title: Delivery Driver This position will be 30 to 40 hours a week from 9am to 5:30 pm M-F Responsibilities: • Operate the company vehicle to transport goods to designated locations. • Adhere to assigned delivery schedules and routes. • Verify orders prior to delivery and obtain necessary signatures upon completion. • Maintain the cleanliness and proper functioning of the vehicle. • Provide courteous and professional customer service at all times. • Place contents of returned packages in necessary containers and photograph incoming contents on a tablet or phone • Able to apply policies and procedures; performs job safely with respect to others and to individual safety, and works effectively with others. • Maintain the vehicle clean at all times Qualifications: • Valid driver’s license with a clean driving record with at least three (3) years of clean driving records • no criminal record and be legally authorized to work in USA without requiring sponsorship • Strong organizational and time-management skills. • Ability to lift and carry packages weighing up to [20 lbs/kg]. • Reliable, punctual, and attentive to detail. • Must be able to concentrate and pay attention to detail • Non-smoker Please submit your resume for consideration