Role Description The Medical Science Director, Oncology is responsible for developing and delivering high-quality, scientifically accurate medical education content for healthcare professionals. This role combines expertise in oncology, medical writing, and adult learning principles to create impactful digital, live, and hybrid programs. Working closely with internal teams, clients, and thought leaders, the Director ensures content aligns with clinical standards, program goals, and industry regulations—helping advance knowledge and improve patient outcomes. Qualifications - Minimum 3 to 5 years’ experience in developing digital, live, in-person, and hybrid medical education programs for HCPs - At least 3 to 5 years’ experience as a medical writer/content developer at a medical education/communications agency - Preference given to individuals with prior Medical Affairs experience - Established expertise in hematology/oncology - Experience in non-malignant hematology, rare diseases, and/or other therapeutic areas a plus - Excellent organizational skills, with a track record of meeting deadlines and driving team success in a fast-paced, deadline-driven environment - Highly proficient in written English and verbal communication skills; additional languages a plus - Highly proficient with Microsoft Office suite - particularly PowerPoint - with excellent editorial skills (writing and editing) - An advanced degree in a medical or science-related specialty (MD, PharmD, RN, NP, PA, PhD) is preferred; a Bachelor of Science degree (life sciences, public health, or clinical sciences) with several years’ relevant work experience required Requirements - Create high-quality scientific, medical, and/or clinical content for physicians, nurses, pharmacists, and other healthcare providers - Develop PowerPoint presentations, text-based copy, and other project-related deliverables for multimedia programs across digital, live virtual, and/or in-person formats - Maintain up-to-date knowledge of key clinical issues within the therapeutic areas of interest; remain current with relevant literature; clinical practice guidelines; approved therapeutic drugs, regimens, and devices; and therapeutic pipelines - Develop and maintain professional relationships with thought leaders and expert faculty in the specified therapeutic areas to deliver current, accurate, and compelling content - Ensure content alignment with program goals and client expectations - Write assessment/survey/polling questions aligned with project goals; analyze program data/outcomes to develop compelling insights and presentations - Serve as a consultant to internal teams and clients to design and execute programs that are clinically appropriate, instructionally-sound, and adherent to industry regulations - Support application of adult learning theory, instructional design principles, and best practices for health care provider education for specified projects - Support engagement with internal stakeholders and clients to identify program goals and establish measurable indicators for success - Engage with Sales and Strategy colleagues to provide recommendations for future programs - Meet regularly with team members to review work quality, client satisfaction, productivity metrics, and progress toward project-related objectives - Demonstrate accountability against defined performance standards for working with internal teams and clients - Complete projects within established timelines and to specifications Benefits - Health Insurance (medical, dental, and vision coverage) - Paid Time Off (including vacation, sick leave, and flexible holiday days) - 401(k) Retirement Plan with employer matching - Life and Disability Insurance - Employee Assistance Program (EAP) - Commuter and/or Transit Benefits (if applicable) - Eligibility for specific benefits may vary based on job classification, schedule (e.g., full-time vs. part-time), work location and length of employment

Role Description At our company, we aspire to be the premier research-intensive biopharmaceutical company. We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We are seeking a dedicated and knowledgeable Virology (HIV) Community MSL / Regional Medical Scientific Director to join our team. This remote position will cover: - Base in Massachusetts or Connecticut - Upstate NY - Western PA (Pittsburgh) - OH - WV If you are passionate about making a difference in the field of Virology and HIV, we invite you to apply and be part of our mission to save and improve lives around the world. Qualifications - A doctorate degree or advanced practice professional (PhD, PharmD, NP/PA, etc.) relevant to Virology and requirements of the position. - A minimum of 3 years prior experience in the biotech/pharmaceutical or healthcare environment. - A minimum of 3 years of clinical and/or research experience in Virology/HIV or related therapeutic area. - Excellent interpersonal, communication, networking, and presentation skills. - Ability to travel up to 50% of the time overnights and reside in the coverage region. - Deep therapeutic competency; abreast of trends and new information in Virology. - Ability to network and partner with important external scientific leaders and healthcare providers. - Ability to consolidate and understand complex data sets, plan and/or execute data analyses, summarize or synthesize data, and objectively interpret results. - Knowledge of national and society treatment guidelines, clinical research processes, FDA regulations, and OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry. - Must be able to organize, prioritize, and work effectively in a constantly changing environment. Requirements - Awareness of the unmet needs and implementation barriers of priority populations that receive services within community-based and non-medical spaces. - Prior working experience within the coverage region and established relationships with HIV community stakeholders, especially in the HIV prevention space. - Demonstrable effective leadership skills. - Strong working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel). Benefits - Medical, dental, vision healthcare and other insurance benefits (for employee and family). - Retirement benefits, including 401(k). - Paid holidays, vacation, and compassionate and sick days.

• Work within the Medical Affairs organization to identify, establish, and manage collaborative professional relationships with community-based scientific leaders (SLs) and healthcare providers. • Conduct peer-level scientific discussions and maintain a reliable presence to ensure SLs have a Medical Affairs contact within our company. • Engage in proactive non-product discussions regarding scientific issues to understand real-world prevention gaps, persistent disparities, and barriers to uptake across various care settings. • Facilitate appropriate scientific exchange of information with SLs, including integration of scientific knowledge with actionable insights to inform our Company's research, development and strategies. • Communicate external stakeholder opinions, insights, and feedback on new data, clinical trends, and the evolving HIV treatment and prevention landscape to Medical Affairs HQ teams. • Represent R&D at scientific meetings and congresses to understand the sentiment of the consumer and contribute to R&D debriefs, insight discussions, and post-congress reports. • Develop and execute territory plans in alignment with global Virology strategy. • Support data generation activities when requested by R&D leadership, including our company's Investigator Study Program (MISP). • Identify potential investigators for participation in phase II-IV clinical development programs and provide scientific support for R&D sponsored trials as needed. • Demonstrate and maintain in-depth knowledge of the assigned disease and therapeutic area(s) through educational efforts. • Fully comply with all company policies and applicable laws, regulations, and ethical standards.

• Interact with clinical investigators and thought leaders to design a clinical development plan for nominated drug candidates • Lead internal study teams, and partner with investigators and CROs to design and implement clinical studies • Work closely with GPLs to ensure development and commercial optimization of Rayze Bio assets • Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and regulatory documents • Conduct investigator meetings and lead site qualification and initiation visits with clinical trial investigators • Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets • Translate findings from research and nonclinical studies into clinical development opportunities • Oversee Data Review and Independent Data Monitoring Committees • Conduct clinical trials using ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines • Establish and maintain positive relationships with clinical trial investigators and thought leaders • As needed serve as clinical lead for regulatory interactions, including preparation of briefing documents and attendance and presentation at health authority meetings. Oversee regulatory submissions for assets in prostate cancer indications • Lead cross-functional study teams and supervise and mentor clinical scientists and medical directors in executing the programs for prostate cancers. • Recruit and build and manage team of medical directors and clinical scientists as needed based on programmatic needs • Leverages AI to drive program, portfolio, or functional performance through prioritization and scaled adoption • Willing to travel approximately 30% of the time.