Title: Clinical Trial Activation Specialist Location: Houston United States Job Description: The Division of Clinical Research provides infrastructure support for all aspects of clinical research. UT MD Anderson has the nation's largest cancer clinical trials program enrolling patients in Texas and beyond through our Cancer Network partners across the country. The Clinical Trial Activation Specialist oversees the clinical trial activation process at MD Anderson. Acts as a liaison between different central departments and research teams throughout the lifecycles of the clinical study. Maintains real-time tracking of the progress and milestones of assigned trials and proactively alerts to potential delays. Responsible for confirming all institutional requirements are met prior to activation/implementation. The ideal candidate will have prior experience in regulatory compliance or clinical research start-up. Minimum $29.09 - Midpoint $36.30 - Maximum $43.51 per hour based on a 40-hour work week. Work location: Remote. Why Us? UT MD Anderson offers the opportunity to support groundbreaking clinical research while working in a collaborative, mission-driven environment. This role allows the Clinical Trial Activation Specialist to directly contribute to accelerating clinical studies that improve outcomes for patients with cancer, while benefiting from a remote work arrangement that supports work-life balance and long-term professional growth. - Employer-paid medical coverage starting day one for employees working 30+ hours/week, plus optional group dental, vision, life, AD&D, and disability insurance. - Accruals for PTO and Extended Illness Bank, plus paid holidays, wellness, childcare, and other leave options. - Tuition Assistance Program after six months of service and access to extensive wellness, fitness, and employee resource groups. - Defined-benefit pension through the Teachers Retirement System, voluntary retirement plans, and employer-paid life and reduced salary protection programs. Responsibilities Activations and Modifications Support (70%) Responsible for the facilitation of protocol acceptance, activation, and modification implementation for clinical research protocols. - Facilitate protocol acceptance, activation, and modification implementation for clinical research studies. - Oversee effective operation of protocols involving collaboration with clinical research administration, departments, and central offices. - Serve as the primary resource for maintaining study status information across assigned trials. - Document delays in activation and identify bottlenecks in activation and implementation processes. - Manage new study submission and activation after confirming all institutional requirements are met. - Develop and maintain a tracking system to monitor protocol activations and modifications. Communication (20%) - Maintain up-to-date status updates between central offices, research staff, and departments throughout the study life cycle. - Navigate protocols through clinical research systems by coordinating with multiple stakeholders. - Prepare for and attend clinical department meetings for assigned departments. - Serve as a content expert to guide departments through the activation process. Maintenance of Regulatory and Study Documentation (10%) - Assure appropriate written regulatory documentation and standard operating procedures are maintained. - Maintain up-to-date knowledge of institutional policies, databases, and systems used in clinical trial workflows. - Utilize systems such as CTMS, the IRB system, and other indicated research platforms. Other Duties - Perform other duties as assigned to support clinical research at UT MD Anderson. EDUCATION - Required: Bachelor's Degree - Preferred: Master's Degree WORK EXPERIENCE - Required: Four years in regulatory compliance or clinical research start-up - May substitute education degree with additional years of experience on a one to one basis LICENSES AND CERTIFICATIONS - Required: CCRP - Certified Clinical Research Professional or CCRC - Certified Clinical Research Coordinator or CCRA - Certified Clinical Research Associate The University of Texas MD Anderson Cancer Center offers excellent benefits, including medical, dental, paid time off, retirement, tuition benefits, educational opportunities, and individual and team recognition. This position may be responsible for maintaining the security and integrity of critical infrastructure, as defined in Section 113.001(2) of the Texas Business and Commerce Code and therefore may require routine reviews and screening. The ability to satisfy and maintain all requirements necessary to ensure the continued security and integrity of such infrastructure is a condition of hire and continued employment. It is the policy of The University of Texas MD Anderson Cancer Center to provide equal employment opportunity without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, disability, protected veteran status, genetic information, or any other basis protected by institutional policy or by federal, state, or local laws unless such distinction is required by law.http://www.mdanderson.org/about-us/legal-and-policy/legal-statements/eeo-affirmative-action.html Additional Information - Requisition ID: 180501 - Employment Status: Full-Time - Employee Status: Regular - Work Week: Days - Minimum Salary: US Dollar (USD) 60,500 - Midpoint Salary: US Dollar (USD) 75,500 - Maximum Salary : US Dollar (USD) 90,500 - FLSA: exempt and not eligible for overtime pay - Fund Type: Soft - Work Location: Remote - Pivotal Position: Yes - Referral Bonus Available?: Yes - Relocation Assistance Available?: Yes #LI-Remote

Role Description We are sharing a specialised part-time consulting opportunity for medical professionals experienced in diagnostic imaging, radiology, pathology, clinical image interpretation, reference solution writing, and structured medical review. This role supports current and upcoming remote consulting opportunities focused on structured diagnostic interpretation, medical image review, clinical reasoning assessment, technical task development, reference solution preparation, and high-quality project execution. Selected professionals will apply their diagnostic expertise to author, review, and annotate technical tasks involving radiologic, pathologic, and clinical images. Key Responsibilities - Diagnostic Imaging & Clinical Image Review - Review medical materials involving CT, MRI, plain film, ultrasound, histopathology, or other clinical images. - Interpret diagnostic findings accurately and connect them to clinically appropriate reasoning, differential diagnosis, and expected conclusions. - Identify missing findings, interpretation gaps, image-quality issues, and expected diagnostic outcomes. - Support structured review of image-grounded medical and clinical interpretation tasks. - Problem Authoring & Reference Solution Development - Create original diagnostic interpretation tasks based on radiologic, pathologic, and clinical images. - Write clear reference solutions with clinically sound reasoning, appropriate terminology, and evidence-based interpretation. - Develop tasks involving diagnostic reasoning, image interpretation, clinical context, and specialty-specific review. - Ensure diagnostic tasks are precise, clinically appropriate, and aligned with source images. - Annotation, Review & Quality Checks - Annotate diagnostic tasks according to structured medical review criteria. - Apply quality checks to assess correctness, clarity, clinical relevance, image grounding, and solution completeness. - Review answer keys, diagnostic explanations, image-based prompts, and clinical interpretation materials for consistency and accuracy. - Maintain high standards for clinical judgment, technical writing, and medical review quality. Qualifications - Board certification in radiology, pathology, or an equivalent imaging-focused medical specialty. - MD/DO with fellowship training in an imaging-heavy specialty or 3+ years of active clinical practice involving diagnostic interpretation. - Active medical licensure. - Comfort interpreting CT, MRI, plain film, ultrasound, histopathology, or related clinical images at an interpretive level. - Strong ability to write clear, structured clinical explanations. - High attention to detail and ability to evaluate diagnostic reasoning carefully. Educational Background - MD, DO, or equivalent physician qualification is strongly preferred. - Board certification, fellowship training, residency training, or active medical licensure is highly relevant. - Background in radiology, pathology, emergency medicine, oncology, internal medicine, surgery, or another diagnostic-heavy specialty may be relevant depending on imaging experience. Nice to Have - Academic appointment, teaching experience, publication record, or medical education background. - Experience writing clinical cases, diagnostic teaching files, imaging reports, board-style questions, or assessment materials. - Familiarity with structured medical annotation, diagnostic QA, clinical rubric development, or peer review workflows. - Experience interpreting multiple imaging modalities or combining imaging findings with clinical context. - Strong comfort working through detailed, image-based, reasoning-heavy medical tasks with sustained focus. Why This Opportunity - Apply diagnostic imaging and clinical interpretation expertise to structured remote project work. - Contribute to high-quality medical image review, diagnostic task authoring, reference solution writing, and clinical evaluation. - Work on flexible part-time assignments aligned with your medical specialty. - Use your clinical judgment in a rigorous, detail-oriented review environment. - Remote structure with competitive hourly compensation. Contract Details - Independent contractor role. - Fully remote with flexible scheduling. - Part-time commitment of approximately 20 hours per week depending on project availability. - Competitive rates between $130–$155 per hour depending on expertise. - Weekly payments via Stripe or Wise. - Projects may be extended, shortened, or adjusted depending on scope and performance. - Work will not involve access to confidential or proprietary information from any employer, client, or institution. About the Platform This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams.

Role Description We are sharing a specialised part-time consulting opportunity for nursing professionals experienced in patient care, clinical monitoring, medication administration, clinical documentation, care coordination, and structured healthcare workflow review. This role supports current and upcoming remote consulting opportunities focused on nursing-related clinical review, patient care workflow evaluation, documentation assessment, medication administration scenarios, clinical data review, and high-quality project execution. Selected professionals will apply their nursing expertise to review realistic healthcare scenarios, evaluate clinical outputs, prepare structured written feedback, and support accurate, evidence-based nursing workflow tasks. Key Responsibilities - Patient Care & Clinical Monitoring Review - Review nursing scenarios involving patient care, clinical monitoring, vital signs, care plans, escalation pathways, and patient status updates. - Evaluate clinical outputs against source materials, nursing standards, patient context, and documented review criteria. - Support structured review of bedside care workflows, triage notes, patient assessments, nursing observations, and follow-up documentation. - Identify missing clinical context, documentation gaps, care-sequence issues, and expected nursing review outcomes. - Medication Administration & Documentation Support - Review scenarios involving medication administration, MAR documentation, dosage timing, patient instructions, adverse-event monitoring, and clinical handoffs. - Evaluate nursing documentation for clarity, accuracy, completeness, and alignment with patient care requirements. - Support structured review of nursing notes, medication records, care summaries, discharge instructions, and clinical communication materials. - Prepare clear written feedback based on source materials and verifiable clinical criteria. - Clinical Workflow Evaluation & Structured Feedback - Review nursing-related tasks and deliverables based on real-world patient care and healthcare documentation workflows. - Provide domain-specific feedback on clinical accuracy, patient safety, workflow realism, and communication quality. - Support evaluation workflows involving AI-generated nursing summaries, care recommendations, documentation outputs, and clinical reasoning. - Maintain accuracy, consistency, and professional judgment across submitted work. Qualifications - Professional nursing experience in patient care, clinical monitoring, medication administration, documentation, care coordination, or healthcare operations. - Background in one or more areas such as acute care, primary care, emergency care, long-term care, behavioral health, pediatrics, surgical nursing, oncology, ICU, or community health. - Familiarity with nursing workflows involving patient assessment, medication administration, clinical documentation, care planning, handoffs, and escalation protocols. - Comfort reading and preparing nursing artifacts such as patient notes, MAR records, care plans, handoff summaries, discharge instructions, and clinical documentation. - Strong written communication skills. - Ability to work independently in a remote, project-based environment. Educational Background - Nursing education, RN/LPN/LVN qualification, BSN, MSN, or equivalent clinical training is helpful. - Active or prior nursing licensure is highly relevant depending on project scope. - Equivalent practical experience in nursing, clinical documentation, patient care review, healthcare QA, or care coordination is also valuable. Nice to Have - Experience in hospital, clinic, long-term care, home health, case management, telehealth, or healthcare quality environments. - Familiarity with EHRs, clinical documentation standards, medication administration records, care pathways, discharge planning, or patient safety workflows. - Experience preparing or reviewing nursing notes, care plans, patient summaries, handoff documentation, medication records, or clinical review materials. - Certifications such as RN, BSN, MSN, CCRN, CEN, CMSRN, or related nursing credentials are helpful. - Strong attention to detail in clinical, patient-facing, and documentation-heavy healthcare environments. Why This Opportunity - Apply nursing expertise to structured remote clinical review work. - Contribute to high-quality nursing workflow evaluation, patient care review, and healthcare documentation assessment. - Work on flexible assignments aligned with your clinical background. - Use your nursing judgment in a focused, evidence-based review environment. - Remote structure with competitive hourly compensation. Contract Details - Independent contractor role. - Fully remote with flexible scheduling. - Part-time commitment depending on project availability. - Competitive rates between $65–$95 per hour depending on expertise. - Weekly payments via Stripe or Wise. - Projects may be extended, shortened, or adjusted depending on scope and performance. - Work will not involve access to confidential or proprietary information from any employer, client, or institution. About the Platform This opportunity is available through 24-MAG LLC. We connect experienced professionals with remote consulting opportunities across technical, evaluation, and project-based workstreams. By submitting this application, you acknowledge that your information may be processed by 24-MAG LLC for recruitment and opportunity matching in accordance with our Privacy Policy: https://www.24-mag.com/privacy-policy .

• Support end-to-end execution of clinical studies (start-up through closeout) • Manage day-to-day study activities across sites, CROs, and vendors • Ensure protocol adherence and high-quality data collection • Collaborate with Medical Affairs, Quality Assurance, Regulatory Affairs, and Marketing/Market Access • Track study budgets and forecasts • Support Regulatory in IDE pathways and study requirements