Role Description The Associate Director will serve as a scientific ambassador for Drug Hunter, enabling and educating members through platform demos, onboardings, workshops, and live events while producing and refining high-quality educational and data content. This role partners closely with the growth teams to deliver compelling presentations, support member engagement, and represent Drug Hunter at industry gatherings, with frequent travel and a strong external-facing presence. Key Responsibilities - Member Enablement & Education - Lead platform demonstrations for drug discovery professionals across seniority levels and functional areas—from bench scientists to CSOs. - Educate Drug Hunter members on best practices and use cases for day-to-day implementation of Drug Hunter through onboarding and workshops. - Design and deliver scientific presentations based on Drug Hunter content and industry knowledge. - Contribute to the production of video and audio content for educational and marketing purposes. - Scientific Communication & Content - Design and deliver presentations for the Drug Hunter Drug Discovery Course in collaboration with project lead. - Provide monthly data analysis articles based on Drug Hunter proprietary data. - Author, edit, and review weekly educational articles drawing on Drug Hunter platform insights. - Host “How to Use Drug Hunter” Events as well as Flash Talks. - Edit and review educational resources, including cheat sheets and Flash Talk follow-up articles. - Cross Functional Collaboration - Represent and help organize Drug Hunter industry mixers, dinners, workshops, symposia, and other networking events. - Own the review process to promote Drug Hunter articles, events, and webinars. - Scientifically review and edit sales enablement materials and collaborate within growth team to share appropriate materials with prospects and members. - Other duties as required. Qualifications - Ph.D. in chemistry, pharmacology, biochemistry, or a related scientific field. - 7+ years of experience in the pharmaceutical or biotechnology industry, with a focus on drug discovery, ideally with project leadership experience. - Credible external presence: comfortable presenting live, fielding skeptical Q&A, and representing the brand. - Strong scientific speaking, writing, editing, and data synthesis skills. - Ability to independently research and distill complex scientific topics for a professional audience. - Digitally native, comfortable with social media, software, databases, literature search tools, and new technologies and platforms. - Ability to collaborate effectively across teams in a remote work environment. - Ability to work independently and collaboratively in an extremely fast-paced, dynamic environment and meet strict deadlines. Preferred Qualifications - Familiarity with Drug Hunter's platform and tools. - Established network within the pharmaceutical and biotechnology industries. - Experience with scientific content creation and data analysis. Requirements - Requires frequent travel. Benefits - Competitive salary, variable compensation, and equity. - Broad range of medical, dental, vision, and life insurance plans for employees and their dependents. - Short-term disability and long-term disability insurance. - Cancer and critical illness coverage. - Up to 14 weeks paid parental leave (after 1 yr tenure) and childcare FSA plan. - 401(k) + employer match (3-5%). - Home office set up stipend for fully remote employees. - Learning and development support. - Generous and flexible vacation and leave policies. To Apply Your application should include: - A resume or CV. - Develop and present a slide deck on a molecule of your choice, highlighting surprising scientific insights, key design lessons, or unexpected development learnings. Applications are considered on a rolling basis.

• Responsible for the operational management and oversight of clinical investigative sites and clinical monitoring deliverables of clinical trials • Ensures that clinical monitoring activities are performed to the Sponsor’s satisfaction, ensuring timely quality deliverables • Identifies quality issues and trends related to site performance and clinical monitoring activities • Summarizes findings and establishes action plans for corrective actions • Serves as a point of contact for CRAs and Lead CRAs for assigned projects • Provides mentoring and oversight of CRAs and Lead CRAs • Performs site visit report review for assigned projects • Contributes to the development of the Clinical Monitoring Plan • Prepares and conducts project-specific training for CRAs • Develops annotated site visit reports and monitoring tools • Conducts quality control visits with CRAs • Coordinates and leads CRA meetings • May be involved in business development activities

• Represent the Biostatistics function for complex studies or at project level • Independently contribute to the design of early/late-stage protocols across multiple therapeutic areas • Draft protocols or amendments, develop and write statistical analysis plans, perform statistical analyses for interim and final reports to be submitted to regulatory agencies • Support submission activities, including design, analysis, and reporting of integrated summaries for safety and efficacy • Attend study team meetings or project level meetings if needed • Contribute to the organization and scheduling of study deliverables in collaboration with Statistical Programmers and Data Managers

• Lead or co-lead one or more complex clinical trial(s) in a therapeutic area for one or more compounds • Contribute to the development of the program strategy for assigned trials/compounds and participate in the development of the clinical development plan (CDP) • Author components with Medical Director and reviewer of clinical and regulatory documents and registration dossiers (i.e., protocol, ICF, IB, safety updates, study reports, regulatory submissions, etc.) to support registration and commercialization of the compound(s) • Contributes in the development of case report forms (eCRFs), eCRFs completion guidelines, and provide scientific support for other key data management deliverables (e.g. database lock activities). • Lead the development of medical data review plan (MDRP), perform ongoing data review, and summarize efficacy and safety data for interpretation/analysis • Provide medical input for country/site selection, feasibility assessment and engage in KOL interaction • Prepare charters and coordinate internal/external committee meetings including presentation preparation (i.e., Dose Escalation, DMC, Steering Committee, Safety) • Participate in the development and review of study plans and serve as a liaison to project teams and CROs • Prepare presentations for Investigator meetings, CRO/CRA training, SIVs as warranted • Provide input for the development of publications in coordination with Scientific Communications • Perform training at Investigator meetings, CRO/CRA training, SIVs as warranted