• Provide strategic input to guide creation of clinically relevant educational content and ensure effective use of clinical data to reach strategic brand objectives • Independent scientific content development including analysis and interpretation of clinical data across a wide range of project types • Conduct literature searches, proactively monitor competitive landscape and perform competitive analyses • Establish strong relationships with clients and proactively seek to contribute and collaborate in client meetings • Partner with internal teams to create compelling peer-to-peer educational content and engagement projects for healthcare professionals, including slide decks, KOL video, digital and print media • Establish close partnership with copy, art and digital teams to create interactive, engaging programs utilizing scientific storytelling techniques and unique data visualization • Collaborate to create and communicate Intouch’s POV and recommendations with clients • Play key role on team to educate team members on disease state, clinical trials, treatments and competition • Support submissions for client medical/regulatory approval processes and partners with all teams to incorporate client and regulatory feedback • Demonstrate a commitment to diversity, equity, and inclusion through continuous development, modeling inclusive behaviors, and proactively managing bias. • All other duties as assigned

• 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.

• 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.