Role Description The primary purpose of the Development Scientist will be to participate in the development of clinical strategies for assigned modalities or indications within the division. This position will work closely with the Global Medical Lead (GML), Operations Lead, and Development Physician, and is accountable for the design, implementation, monitoring, and analysis of clinical studies conducted within the assigned program. Development Scientists are expected to perform their responsibilities independently and have core knowledge of clinical development to enable increased participation in division and portfolio level initiatives. Role and Responsibilities: - Responsible and accountable for activities related to all current and planned clinical trials (e.g., develop protocols, investigator brochures, CRFs, informed consents, and clinical study reports and review of clinical trial documents, study analyses, and reporting) on assigned development programs. - Provides expertise to cross-functional team members to synthesize/contextualize data to facilitate discussion and timely decision making. - Serves on the clinical sub-team with GML, Operations Lead, and Medical Monitor/Study Physician and supports preparation of clinical development plans, site identification and management, and DESC meetings. - Under the guidance of development physician/GML, performs medical monitoring activities (Review, analyze and triage patient data, generating reports). - Able to independently lead working groups and/or sub-team initiatives in support of protocol, disease area, or clinical development plan. - Partners with GML in preparing for Health Authority (HA) Meetings and assists in addressing HA inquiries. - Together with the GML and Product Responsible Person may prepare analysis for DMC/DSMB/DEC forums or regulatory submissions. - Provides training at investigator meetings and site initiation visits with clinical trial staff, and partners with Clinical Operations and Medical Affairs in enabling appropriate enrollment into the clinical studies or registries. - Collaborates cross-functionally to create, review, and/or present clinical slides for internal meetings and external forums. - Supports engagement with potential and current sites (e.g. SIVs, investigator meetings, conferences, steering committee, advisory board meetings). - Exhibits expertise related to Study Data Review and Analysis: - Provides clinical input into statistical planning, data analysis and interpretation. - Provides clinical leadership and support for publication of data (manuscripts, presentations) and disease or technology related scientific publications. - Works closely with operations group for site and vendor feasibility, trial set up and monitoring. - May lead the execution of contracts, particularly for investigator meetings and advisories. - Supports efforts to develop strategic partnerships with Key External Experts (KEEs). - Serve as key partner for Development Division in assessment of candidates within discovery, identifying opportunities and potential risks with future development strategies based on modality, indication, unmet need, competitive landscape and clinical characteristics. - May represent development and assist with clinical assessment for due diligence(s) of new assets for potential in-licensing and acquisition. - Supports strategic initiatives related to assigned molecule(s), CDP, therapeutic area(s), or portfolio, if requested. - Performs other duties as assigned or special projects as needed. Qualifications - Advanced degree in a relevant scientific discipline; health science or clinical discipline with typically 5-7 years clinical, scientific/research, pathology or industry related experience or combination of academia and industry. - Thorough knowledge and demonstrated expertise in biotechnology/pharmaceutical industry related to clinical drug development (early-stage development through approval) from initial study design, study execution and regulatory submissions (INDs, BLAs, NDAs) with US and OUS regulatory agencies. - Experience in scientific research and/or clinical practice (as evidenced by appropriate qualifications, publications and/or relevant accreditations). - Strong computer skills including MS Office Suite (Word, Excel, PowerPoint, Outlook, MS Teams and MS Project) and in the use of industry-standard software (e.g. electronic data capture systems [RAVE, InForm, etc.]) and proficient in data analysis software (Excel, SigmaPlot, SPSS, R, etc.). - Strong collaboration and interpersonal communication skills; able to interact with all levels of internal stakeholders and key functional areas including, Regulatory Affairs, Medical Affairs, Clinical Operations, Data Sciences, Research, Translational Science and Pharmacovigilance (PV). - Demonstrated success working with key external stakeholders (e.g., KEEs, investigators, researchers) including presenting/responding to health authorities. - Knowledge of global pharmacovigilance standards and guidance documents. - Comfortable working in a flexible, dynamically changing and (at times) challenging environment. - Excellent strategic planning, organizational and verbal and written communication skills. - Ability to exercise sound judgment, tact, diplomacy and professionalism in all interactions. - Aware of cultural diversity and how to influence and manage in a multi-cultural organization. - Highest level of scientific integrity and impeccable work ethics. Requirements - M.D. or PharmD degree, or other relevant Master’s degree. - Knowledge and proficiency related to Medical Affairs activities including registries. Benefits - Medical, Dental and Vision Insurance. - Generous Paid Time Off options, including Vacation and Sick time, plus national holidays including year-end shut down. - 401(k) match and annual company contribution. - Company paid life insurance. - Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions. - Long Term Incentive Plan for eligible positions. - Company fleet vehicle for eligible positions. - Referral bonus program.

• Serve as the lead Clinical Research SME for the engagement, guiding all aspects of the operational assessment and change management strategy. • Conduct in-depth interviews with clinical research staff and stakeholders across the clinical trial lifecycle to identify operational gaps, bottlenecks, communication challenges, and improvement opportunities across Oncology and Non-Oncology programs. • Partner with executive and operational stakeholders to assess organizational readiness for change and recommend sustainable transformation strategies. • Collaborate with the Vitalief team to design effective interview templates, assessment methodologies, and change management frameworks. • Evaluate current-state workflows, governance structures, staffing models, and technology utilization to identify opportunities for operational alignment and standardization. • Compare Oncology and Non-Oncology operations to identify transferable best practices and opportunities for cross-functional integration. • Develop prioritized, actionable recommendations that address immediate operational challenges while supporting long-term scalability and organizational adoption. • Create and present a clear transformation roadmap focused on operational excellence, stakeholder engagement, process optimization, and effective cross-system coordination. • Provide regular project status updates to executive stakeholders, ensuring alignment, transparency, and on-time delivery of engagement milestones. • Deliver executive-level presentations summarizing findings, recommendations, change impacts, and measurable next steps.

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.