• Provides clinical development and medical leadership/oversight of clinical programs to ensure timely delivery of clinical deliverables. • Ensures clinical programs support patient safety and provides oversight of patient safety in clinical studies. • As the primary medical expert for assigned study(ies), they are the first point of contact internally and externally for questions regarding the study (e.g. eligibility, enrollment; safety and patient management). Monitors study progress to ensure proper study conduct and adherence to the protocol, leads data review, evaluation, and analyses with support from the cross functional team. Takes a key role in the authoring of critical study documents (e.g., CSR, IB, protocol synopsis). • Contributes to the analysis and interpretation of data generated internally or externally and present study updates, interim results, and final headline data to senior management as required. • Provides medical input and contributes to the clinical development sections of regulatory documents such as IND, CIOMS, DSUR, Dossiers, and contributing to responses to regulatory agencies regarding questions about complex clinical development issues (e.g., safety or efficacy). • Contributes to the cross functional development of clinical development plans (CDPs) that integrate pre-clinical, early clinical findings and data sciences approaches - working to ensure cross-functional alignment on an ongoing basis throughout the phases of clinical development. • Collaborates with teams on the development of translational and precision phenotyping strategies and contributes to the design of scientifically rigorous clinical development studies and programs utilizing a data biopsy signature/precision phenotype approach. Ensures that teams appreciate the clinical relevance and applicability of the approaches considered. • Identifies and engages with external Key Opinion Leaders to address scientific and medical questions relevant to the program. • Helps identify global study sites and foster relationships with study investigators. • Ensures that Serious Adverse Events are properly reported. • Implements clinical R&D policies, SOPs, and related directives. • As required, supports any needed due diligence of potential in-licensing drug candidates and/or technologies and present recommendations to leadership.

Role Description Looking for a NP/PA hire for addiction treatment centers in San Fernando Valley, CA. - Telehealth visits - FT Mon-Fri or PT available - $80/hour - possible salary for FT - Flexible hours Essential Duties include but not limited to: - Assesses patients' mental and physical status based on the presenting symptoms and complaints - Documents patients' medical and psychological histories, physical assessment results, diagnoses, treatment plans, prescriptions, and outcomes - Writing prescriptions for psychotropic and detox medications as allowed by state regulations and collaborative practice agreements - Evaluate patients' behavior to formulate diagnoses or assess treatments Qualifications - Strong skills to manage, coordinate, and evaluate the care and education of the patient - Trained to adhere to medications and therapies with protocols - Strong computer skills, telehealth capabilities Requirements - Must possess current Nurse Practitioner or Physician Assistant License - DEA License - Addiction Treatment experience preferred, but not required - MAT Waiver Training completed to prescribe detox medications is preferred - Will consider new grads who are passionate about getting into addiction and psychiatry! Benefits - Flexible hours - Competitive pay ($80/hour or possible salary for FT)

• Lead and execute early/late stage clinical trials for oncology products in development • Participate in the design/planning of clinical studies and help with the interpretation of study results • Establish and approve scientific methods for design and implementation of clinical protocols, data collection systems and final reports • May recruit clinical investigators for research studies • Monitor adherence to protocols and determine study completion

• The Medical Director actively uses their medical background, experience, and judgement to make determinations whether requested services, requested level of care, and/or requested site of service should be authorized at the Inpatient level. • Provides medical interpretation and determinations whether services provided by other healthcare professionals are in agreement with national guidelines, CMS requirements, Humana policies, clinical standards, and (in some cases) contracts. • Supports and collaborates with other team members, other departments, Humana colleagues and the Lead Medical Director. • Conducts post-service, inpatient care reviews for accurate billing of clinically valid diagnoses and care received. • Engages in disputes and grievance and appeals reviews. • Participates on project teams or organizational committees.