• Stay ahead of payer changes. Review and interpret updates to various payer manuals and translate them into clear guidance for our clinical team • Review and approve all treatment plans. Serve as the final clinical approver of treatment plans and reassessment (around 100 per month) before they are submitted to payors for prior authorization • Coach and elevate the team. Provide specific feedback to treating BCBAs and Clinical Directors that help them grow and develop as clinicals in their ability to create top tier and compliant treatment plans and other related documentation. • Drive quality and compliance. Track denials, identify trends, and recommend training, templates or workflows that reduce errors and improve outcomes. • Be a resource. Help clinicians understand the “why” behind payer requirements and best practices in ABA.

• Building Strong Client Relationships. You’ll become the trusted guiding hand through a client's healthcare journey by managing complex medical issues, coordinating their care, facilitating best diagnostic and therapeutic treatment options available world-wide, and navigating being their guide to the healthcare system • Demonstrating Strong Clinical Acumen. You’ll offer high level clinical management and education to clients and families in a caring, compassionate manner. • Bring Together the Best Minds: Work closely with clinical and research team members at PHM to identify latest therapies and deliver comprehensive information on medical conditions, medications, treatments, and clinical trials. Articulating needs for collaboration with external care providers, interdisciplinary team resources, and internal team rounding. Networking with key opinion leaders to invite collaboration and build relationships that facilitate our ability to help our clients achieve best care. Managing other clinical staff as it relates to a particular case or service line

• Serve as a subject matter expert and team leader for programs/indications supporting our gene therapy portfolio. • Lead efforts to bridge clinical science and commercial efforts by ensuring strategic alignment across various internal and external functions. • Focus on peer-to-peer interactions, the development and execution of advisory boards, KOL advocacy, congress presence, and medical symposia. • Provide structured feedback to internal teams relative to actionable field insights and advance data generation efforts. • Develop and execute Medical Affairs strategy across sickle cell disease (SCD) and transfusion dependent thalassemia (TDT). • Build external relationships to provide scientific and clinical information on therapies to key HCP and bring actionable insights from KOL and treating physicians. • Engage with industry experts to garner support for scientific messages, clinical research, and product value. • Offer medical expertise and input to cross-functional teams including commercial, clinical, operations, payor, and advocacy. • Support the creation of evidence-based content that enhances patient-provider communication. • Maintain compliance with applicable company policies and regulations.

Title: Biostatistics Director, Medical Affairs Location: Remote - USA Job Description: Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on   In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.    Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work. Job Title Biostatistics Director, Medical Affairs Job Summary: The Director of Medical Affairs Biostatistics is responsible for statistical activities in support of external-facing scientific communication. This includes, but is not limited to, providing scientific and methodological expertise to support medical strategy, publications, and external engagements; serving as the primary point of contact between biostatistics and the Medical Affairs team; collaborating with the team in development of publication strategy plans; maintaining and executing Supplemental Statistical Analysis Plans (SAPs); and assisting as needed with real-world evidence-generating requests. They interact with both internal and external cross-functional study teams to support the scientific communication effort, and partner with unblinded biometrics study team members to deliver needed statistical output in a timely fashion. Responsibilities: · Leads the statistical and statistical programming efforts for medical publications, scientific congresses, and external collaborations · Guides statistical design and analysis for investigator-initiated research and collaborative studies · Provides statistical input to strategic planning of publication strategy plans · Develops and maintains Supplemental SAPs · Provides guidance to Medical Affairs team on all aspects of statistical activities to ensure methodological rigor · Works collaboratively with Medical Affairs, Project Management, Translational Medicine, and other staff to meet scientific communication timelines · Provides feedback to the Medical Affairs team regarding what is and is not possible with available data and partners with the team to brainstorm creative, scientifically sound approaches to address key questions · Interacts with the team to prospectively plan publication strategies for future congresses and manuscript generation efforts. · Works with the team to develop idea-generating analyses, including ad hoc and exploratory data analyses (EDA), to inform scientific insights and evidence-generation opportunities · Serves as the primary point of contact for Medical Affairs requests and collaborates closely with Clinical Biostatistics and Statistical Programming leads on relevant protocols · Assists, as needed, with Health Economics and Outcomes Research (HEOR) and real-world evidence (RWE) evidence-generation requests. Where You'll Work: This is a U.S.-based remote role that will require quarterly, or as needed visits to our San Francisco Office. Qualifications: - PhD in statistics or biostatistics with 8+ years relevant experience in the pharmaceutical / biotechnology industry or MS in statistics or biostatistics with 15+ years relevant experience in the pharmaceutical / biotechnology industry - Experienced in post-approval / Medical Affairs settings - Strong knowledge of statistical methodologies, current drug development trends, and regulatory environments - Strong analytical and problem-solving skills; able to identify and investigate issues and causes independently and formulate potential solutions - Established publication record and experience supporting scientific communication - Able to work effectively in cross-functional, matrixed environments - Excellent written and verbal communication skills, with the ability to engage both technical and non-technical audiences. - Excellent programming skills, including the ability to independently generate publication-ready figures; R and/or SAS programming fluency preferred - Able to work in a fast paced environment At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states. Salary $222,300—$255,000 USD As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return. For USA based roles: Financial & Rewards - Market-leading compensation - 401(k) with employer match - Employee Stock Purchase Program (ESPP) - Pre-tax commuter benefits (transit and parking) - Referral bonus for hired candidates - Subsidized lunch and parking on in-office days Health & Well-Being - 100% employer-paid medical, dental, and vision premiums for you and your dependents - Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA) - Fertility & family-forming benefits - Expanded mental health support (therapy and coaching resources) - Hybrid work model with flexibility - Flexible, “take-what-you-need” paid time off and company-paid holidays - Comprehensive paid medical and parental leave to care for yourself and your family Skill Development & Career Paths: - People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility - We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching - We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities