• Manage clinical trial programs/projects from one or multiple clients • Provide day to day technical and operational leadership to project teams • Provide statistical oversight on projects in the assigned drug development programs/projects • Ensure sound statistical methodologies in study design, sample size estimation, statistical analysis planning, and reporting • Coach, mentor, develop, and provide technical review and advice to less experienced Biostatisticians and Statistical Programmers • Participate in the writing of trial protocols and research proposals • Review and provide input to clinical data management deliverables • Write Statistical Analysis Plans, Statistical Reports • Perform overall Quality Control review on statistical deliverables • Ensure compliance with relevant regulatory requirements • Interact with regulatory agencies and support sponsor in new drug applications

• Lead efforts in resolving day to day work related issues • Provide statistical expertise for design, analysis and reporting of clinical trials • Develop and/or review ADaM dataset specifications • Perform statistical analysis as per SAP • Provide statistical input to Case Report Forms (CRF) design • Properly archive study files in accordance with trial sponsor’s requirements.

LMSW Clinical Supervisor Full Time • Hybrid - US 7640 Dixie Hwy #155, Village of Clarkston, MI 48346, USA Benefits: - 401(k) - Flexible schedule - Free food & snacks - Paid time off - Training & development - Dental insurance - Health insurance - Vision insurance Ellie Mental Health – Clarkston is an independently owned and operated private practice serving both the local Clarkston community and the state of Michigan through our office space and telehealth. We manage almost all of your administrative tasks, including billing, so that you can focus on what you love, client care. Join Our Team: At Ellie Mental Health – Clarkston, you’ll be part of a dynamic team committed to expanding access to high-quality mental health care while embracing values that make the journey meaningful: authenticity, compassion, creativity, humor, acceptance, and determination. We are looking for a compassionate and motivated LMSW to join our growing team! In this role, you’ll provide therapy while also supervising LLMSW's. Please note - we’re only considering fully licensed Approved Clinical Supervisor LMSWs for this position. At EMH you’ll deliver outpatient care in a fully furnished, welcoming clinic space designed to support both client wellness and clinician comfort. We offer a standout W2 pay model (straight commission) with industry-leading compensation. What You’ll Do at Ellie Mental Health – Clarkston: - Deliver Care: Conduct comprehensive mental health intakes, develop treatment plans, and complete timely documentation including diagnoses, treatment plans, and session notes. - Build a Full-Time Caseload: Maintain a minimum of 25 direct client facing hours per week as a full-time clinician, with an initial scheduling availability of 35 hours per week to support caseload growth. - Supervision: Provide supervision to LLMSW's on the team. Required Qualifications & Core Competencies: - Mandatory Licensure for Clinical Practice: Applicants must hold full, unrestricted licensure in the State of Michigan. - Note: Provisional or limited licensure does not meet eligibility criteria. - Advanced Educational Foundation: A master’s degree in social work or related field from an accredited institution. - Clinical Proficiency: Experience in creating and implementing treatment plans, as well as maintaining detailed clinical documentation including case notes and diagnostic updates. - Strong Communicator: Exceptional written and verbal communication skills that support therapeutic effectiveness, collaboration, and client trust. - Professional Boundaries & Integrity: Demonstrated ability to establish and uphold stable, ethical boundaries with clients in a clinical setting. - Timely and Accurate Documentation: Consistently completes session records, service notes, and required documentation promptly. - Inclusive Clinical Approach: Comfortable and confident working with a diverse population across age groups, backgrounds, and presenting issues. - Technology Competence: Proficient in day-to-day office tools and electronic health records (EHR); experience with Valant is a plus! Preferred Qualifications & Expertise: - Private Practice Savvy: Prior experience in a private practice setting equips candidates to thrive. - Supervisory Experience: Background in providing clinical supervision or mentoring to limited licensed clinicians. - Credentialing That Amplifies Access: Fully licensed clinicians who are credentialed with multiple insurance panels and EAPs are especially well-positioned to help us expand care access and reach more individuals in need. - Marketing Mindset & Social Media Fluency: Candidates with experience leveraging social media and community marketing are especially valuable. Your ability to amplify visibility, drive engagement, and connect with local audiences supports both clinic growth and client access. Exceptional Benefits That Support Your Well-Being and Growth: - Generous Paid Time Off - Comprehensive Health Coverage - Holiday Pay - Short-Term Disability Insurance - 401(K) - Free Annual CEUs - Flexible Scheduling Flexible work from home options available. Compensation: $78,000.00 - $110,000.00 per year

Role Description As a Clinical Research Physician (CRP), you'll bring your scientific training and clinical experience to the heart of how we develop and deliver medicines. You'll play a central role across the product lifecycle — from designing and running global clinical trials through to registration, commercialization, and beyond. - Contribute to protocol development, study reporting, and data dissemination. - Review publications, support labeling updates, and help shape documents for pricing, reimbursement, and access. - Ensure adverse events are reported in line with patient safety standards. - Engage with regulatory agencies and external thought leaders to advance our science. - Serve as a key scientific resource — advising study teams and supporting medical activities. - Uphold the highest standards of compliance with applicable regulations (FDA, ICH, CPMP), Good Clinical Practices, Lilly policies, and the Principles of Medical Research. Qualifications - Medical Doctor. Must be board eligible or certified in appropriate specialty/subspecialty or have completed comparable post-medical school clinical training relevant to the country of hiring. - Experience of international oncology practice. - Fluent in English; both written and verbal communications. - Demonstrated knowledge of the drug development process. Requirements - In-depth knowledge of breast oncology. - Experience with CDK 4 & 6 inhibitors. - Demonstrated strong communication, interpersonal, organizational, teamwork, and negotiation skills. - Demonstrated ability to influence others cross-functionally. - Ability to engage in domestic and international travel as needed. - Clinical research or pharmaceutical medicine experience preferred. Company Description Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world. We were founded more than a century ago by a man committed to creating high-quality medicines that meet real needs, and today we remain true to that mission in all our work. - Over 50,000 employees globally. - Focus on discovering and delivering life-changing medicines. - Commitment to improving the understanding and management of disease. - Engagement in philanthropy and volunteerism.