Role Description The Market Behavioral Health Medical Director is responsible for the overall safety of patients with a Behavioral Health diagnosis, with a special focus on safe prescribing. - Assume responsibility for the overall safety of patients with a behavioral health (BH) diagnosis, focusing on safe prescribing practices. - Serve as the psychiatric lead in developing and implementing evidenced based clinical BH policies and practices for the state. - Conduct regulatory and accreditation reviews to ensure compliance with applicable standards. - Oversee BH coverage determination for utilization management, ensuring members receive appropriate and medically necessary care in the most cost-effective setting. - Lead quality improvement initiatives, case management activities and member safety protocols, including incident management. - Review utilization data to identify variances in patterns and provide feedback and education to Managed Care Plan (MCP) staff and providers as needed. - Represent CareSource as the primary psychiatric liaison to members, providers and state agencies. - Participate in the development, implementation and revision of the clinical care standards and practice guidelines ensuring compliance with nationally accepted quality standards. - Contribute to the development, implementation and revision of the Quality Improvement Plan and corporate level quality initiatives. - Collaborate with market and product leaders to define market strategy and enhance the quality and affordability of BH services. - Participate in community collaborative initiatives to improve BH services. - Evaluate and investigate cases suspected of fraud, abuse, and quality of care concerns. - Provide cross-coverage for other Medical Directors and/or markets, as needed. - Support staff through training, clinical consultation, and clinical case review for members, including Medical Advisement meetings. - Advocate for behavioral health in collaboration with the Market's government affairs and regulatory leads to advance CareSource's mission and meet specific advocacy goals. - Strengthen and develop relationships with specialty (CBHC) and IMD (standalone hospital) providers as needed in the Market. - Engage in Market professional society activities to enhance CareSource's objectives. - Consult with Market and Enterprise leadership to improve quality for members through collaborative execution of behavioral health quality improvement activities, including HEDIS and value-based reimbursement contracting. - Act as liaison with state agencies and organizations on BH initiatives, residing in the state market if required. - Perform any other job related duties as requested. Qualifications - Medical Doctor (MD) required or Doctor of Osteopathic Medicine (DO) required. - Successful completion of a residency training program in psychiatry required. - Five (5) years of clinical practice experience required. - Experience in safe prescribing required. - Managed care medical review/medical director experience preferred. - Residence and clinical practice in assigned market may be required preferred. Requirements - Basic Microsoft Word skills. - Excellent communication skills, both written and oral. - Ability to work well independently and within a team environment. - Ability to create strong relationships with Providers and Members. - Previous Institute for Healthcare Improvement (IHI) or equivalent training participation is preferred. - High ethical standards. - Attention to detail. - Critical listening and systematic thinking skills. - Ability to maintain confidentiality and act in the company’s best interest. - Ability to act with diplomacy and sensitivity to cultural diversity. - Decision making/problem solving skills. - Conflict resolution skills. - Strong sense of mission and commitment of time, effort and resources to the betterment of the communities served. - Ability to analyze healthcare data from a variety of sources to evaluate physician practice patterns. - Leadership experience and skills. Licensure and Certification - Current, unrestricted license to practice medicine in state of practice as necessary to meet regulatory requirements required. - Board Certification in Psychiatry required. - Re-certification, as required by specialty board, must be maintained. - MCG Certification is required or must be obtained within six (6) months of hire. Working Conditions - General office environment; may be required to sit or stand for extended periods of time. - Flexible hours, including possible evenings and/or weekends as needed. - Ability to travel as required by the needs of the department. Compensation Range $195,200.00 - $341,600.00. CareSource takes into consideration a combination of a candidate’s education, training, and experience as well as the position’s scope and complexity, the discretion and latitude required for the role, and other external and internal data when establishing a salary level. In addition to base compensation, you may qualify for a bonus tied to company and individual performance. We are highly invested in every employee’s total well-being and offer a substantial and comprehensive total rewards package. Compensation Type Salary Organization Level Competencies - Fostering a Collaborative Workplace Culture. - Cultivate Partnerships. - Develop Self and Others. - Drive Execution. - Influence Others. - Pursue Personal Excellence. - Understand the Business. This job description is not all inclusive. CareSource reserves the right to amend this job description at any time. CareSource is an Equal Opportunity Employer. We are dedicated to fostering an environment of belonging that welcomes and supports individuals of all backgrounds.

• Develop and maintain clinical policies, procedures, and standards that support measurement-based teletherapy at scale • Design systems for ongoing quality assurance, chart review, and clinical performance monitoring • Ensure compliance with regulatory, ethical, documentation, and quality standards • Define clinical hiring standards and assess candidates for alignment with Allminds' care philosophy • Design and oversee clinician onboarding and training programs • Provide clinical leadership, consultation, and supervision across the network • Establish scalable systems for ongoing quality review, case consultation, clinical feedback and professional development • Provide clinical expertise for the development of documentation tools, quality monitoring systems, measurement-based care workflows, AI-enabled clinical support tools, and other innovations • Ensure technology solutions support both excellent patient outcomes and sustainable clinician practices

Role Description This is a remote position that will require up to 20%-25% travel. Candidate can be located anywhere in the United States. The Senior Medical Director – Prostate Cancer Nuclear Imaging will serve as the medical lead for prostate cancer nuclear imaging modalities. This leader will drive the development and execution of medical strategy supporting launch and lifecycle management, ensuring alignment across Clinical Development, Commercial, and Market Access functions. The role requires deep expertise in prostate cancer and nuclear imaging to enable impactful scientific engagement, appropriate use of imaging agents, and optimization of patient outcomes. - Lead the development and execution of integrated medical affairs strategies and tactical plans for prostate cancer nuclear imaging products. - Provide strategic medical leadership to cross-functional teams, ensuring alignment with corporate objectives and launch priorities. - Partner closely with Clinical Development, Commercial, Market Access, Regulatory, and Communications to drive successful product adoption and differentiation. - Serve as the primary internal and external medical expert for prostate cancer nuclear imaging. - Act as a subject matter expert in prostate cancer imaging with specialized knowledge of nuclear imaging technologies (e.g., PSMA PET and other advanced diagnostics). - Collaborate with Clinical Development and R&D to support evidence generation, including imaging endpoints, clinical utility, and health outcomes data. - Partner with Commercial to support product launch by providing scientific leadership, medical insights, and perspectives on healthcare provider and patient needs. - Lead medical programs supporting product launch, including publication strategy, congress planning, scientific dissemination, and evidence generation. - Establish and maintain strong relationships with key opinion leaders, imaging specialists, oncologists, and professional societies. - Facilitate scientific exchange to understand evolving diagnostic paradigms, unmet needs, and clinical practice trends. - Capture and translate external insights into actionable medical strategies and future research initiatives. - Build and lead a high-performing medical affairs team focused on prostate cancer nuclear imaging. - Coach and mentor medical directors and scientific staff, fostering a culture of innovation, excellence, and compliance. - Drive collaboration and alignment across regional and global teams. - Ensure all medical activities adhere to regulatory requirements, corporate policies, and ethical standards. - Oversee budget planning, resource allocation, and operational execution for the medical team. - Define and monitor KPIs to measure the impact of medical strategies and engagement activities. - Must maintain operational compliance with US regulatory agencies and guidelines (primarily FDA and NRC), and collaborate with European based Legal Department colleagues on matters that touch and concern foreign legal/regulatory requirements. Qualifications - Advanced degree (MD, DO, PhD, PharmD, or equivalent) required; specialization in nuclear medicine, radiology, oncology or urology strongly preferred. - Board-certified/eligible nuclear medicine physician or diagnostic radiologist strongly preferred; oncology experience (particularly prostate cancer) highly desirable. - Significant experience in medical affairs, clinical development, or related roles within the biopharmaceutical or imaging space (typically 10+ years). - Demonstrated expertise in prostate cancer and nuclear imaging (e.g., radiopharmaceuticals, PET imaging); clinical experience in nuclear medicine, radiology, or uro-oncology highly desirable. - Proven leadership experience with a track record of building and managing high-performing teams. - Strong experience in product launches, ideally within oncology or diagnostic imaging. - Established relationships with key opinion leaders and professional societies in nuclear medicine and/or oncology. - Excellent communication, strategic thinking, and cross-functional collaboration skills. Requirements - This position will work in typical office conditions with extensive time using personal computer equipment. - May be required to sit or stand for long periods of time while performing duties. - Close attention to detail required. - Willingness to work in a team-based environment. - The position deals with many deadlines. Due to the short turnaround time of deadlines and limited time, overtime, weekend work and holiday work is sometimes required. - Ability to travel domestically and potentially internationally as required. Company Description Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage combined with a pioneering approach are the hallmarks to deliver innovation, excellence and unparalleled service. With manufacturing facilities across Europe and the United States, Curium delivers SPECT, PET and therapeutic radiopharmaceutical solutions for life-threatening diseases to over 14 million patients annually. The name ‘Curium’ honors the legacy of pioneering radioactive researchers Marie and Pierre Curie, after whom the radioactive element curium was named and emphasizes our focus on nuclear medicine. The tagline ‘Life Forward’ represents our commitment to securing a brighter future for all those we serve: An enhanced quality of care for our patients. A trusted partner to our customers. A supportive employer to our valued team.

• Providing medical and scientific oversight for clinical trials, ensuring the safety of subjects and the integrity of trial data. • Collaborating with clinical operations, regulatory, and safety teams to drive the successful execution of early phase clinical studies. • Developing and reviewing clinical study protocols, study reports, and other key study documents. • Interpreting clinical trial data and providing medical insights to inform decision-making and guide clinical development strategies.