• Provides administrative oversight to the medical staff • Analyzes medical review utilization data • Researches new medical procedures or technology • Acts as a resource to providers and internal staff on issues concerning medical policies • Writes and revises medical policies • Supports operations in the form of case review on both medical and regulatory matters • Develops claim adjudication criteria for situations requiring medical judgment • Provides input on issues and operational policies, processes, and procedures • Educates staff and medical community on various aspects of medical policy and program administration • Develops and updates medical policy in consultation with appropriate regulatory personnel, medical consultants, and professional societies • Develops external relationships with the medical community and serves as liaison between these entities and the contractors • Reviews physician and provider practice pattern analysis and other statistical data related to unusual medical service utilization • Conducts research into new or controversial medical procedures and technology

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description The Medical Advisor will provide clinical expertise across product development, consumer education, media representation, and marketing review. This physician will serve as a credible medical voice for the brand while ensuring scientific integrity and regulatory responsibility across all public-facing health content. This is a highly visible role ideal for a physician passionate about preventive health, health equity, and empowering Black women through education. Key Responsibilities - Product Development & Scientific Oversight - Advise on formulation strategy and ingredient selection for new and existing supplements - Review clinical research to support product claims and positioning - Provide guidance on dosing, safety considerations, contraindications, and target populations - Participate in product concept meetings and innovation strategy sessions - Educational Programming - Host monthly virtual educational webinars (Zoom) including live Q&A sessions - Develop educational slide decks and talking points for consumer-facing sessions - Address topics related to women's health, preventive care, and culturally relevant medical concerns - Content Creation & Review - Collaborate on educational social media content (Reels, carousels, short-form videos, lives) - Provide expert commentary on health topics relevant to BGV’s audience - Review health-related messaging and marketing materials, advertising copy, website content for medical accuracy - Brand Representation - Represent Black Girl Vitamins at select conferences, health expos, and brand events - Participate in podcast interviews, media opportunities, and press features as the brand’s medical voice - Contribute quotes for press releases and thought leadership initiatives Preferred Specialties - OBGYN - Uterine Fibroids - Sports Medicine - Oncology (Cancer prevention & survivorship) - Dermatology (with emphasis on hair health and scalp conditions) Physicians with demonstrated experience addressing health disparities are strongly encouraged to apply. Qualifications - Active U.S. medical license in good standing - Board-certified physician (MD or DO) - Minimum 3–5 years of clinical experience - Demonstrated experience in public speaking, media, or patient education preferred - Comfort appearing on video and participating in live Q&A sessions - Strong understanding of supplement regulations and evidence-based claims - Passion for advancing health equity Time Commitment - Approximately 10–20 hours per month (may vary based on campaign cycles and product launches) - Monthly webinar commitment required - Occasional travel for events and conferences Compensation This is a paid independent contractor role. Compensation will be competitive and commensurate with experience, scope of work, and media participation. Speaking engagements and travel will be compensated separately as applicable. Benefits - Be part of a mission-driven brand improving health outcomes for Black women - Shape innovative supplement products grounded in science - Amplify trusted medical education within a culturally relevant platform - Expand your public voice through media and national brand visibility

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. What You'll Do #LI-TC1 As the Senior Director / Executive Director, Regulatory Affairs, you are a driven global regulatory leader with expertise in regulatory strategy development and execution. You excel in navigating global health authority interactions, leading cross-functional teams, and driving clinical and licensing submissions. Reporting to the QED Head of Regulatory Affairs, you will provide leadership in regulatory activities for assigned programs, including developing global regulatory strategies, leading submissions, and managing critical health authority interactions as well as leading regulatory staff. Responsibilities Provide leadership in creating and executing proactive regulatory strategies for product development, approval, and registration Apply knowledge of global quality/regulatory standards and guidelines to ensure requirements are met across programs Who You Are Bachelor's degree in the scientific field is required; an advanced degree (MD, Ph.D., PharmD, MS) preferred A minimum of 15 years of relevant pharmaceutical/biotechnology regulatory affairs experience in the pharmaceutical industry, including expertise leading a Regulatory Affairs group Well-versed in the drug development process and regulatory requirements, as well as a good understanding of the underlying science Strong attention to detail Excellent written and verbal communication skills Excellent project management skills, with the ability to manage multiple projects and prioritize appropriately Ability to rapidly understand & analyze complex problems/situations Ability to lead teams under tight timelines and be willing to contribute significantly to day-to-day operations as needed Comfort in a team environment Strong interpersonal skills and the ability to effectively work with others Ability to influence without authority, lead change Ability to solicit information, persuade others, and shape outcomes Experience working with all levels of management and consulting with key business stakeholders (internal and external) Travel to key meetings and Health Authority interactions as needed You have demonstrated curiosity and adaptability in adopting AI-powered tools and technologies Rewarding Those Who Make the Mission Possible We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return. Financial Benefits: Market leading compensation 401K with 100% employer match on first 3% & 50% on the next 2% Employee stock purchase program Pre-tax commuter benefits Referral program with $2,500 award for hired referrals Health & Wellbeing: Comprehensive health care with 100% premiums covered - no cost to you and dependents Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions) Hybrid work model - employees have the autonomy in where and how they do their work Unlimited flexible paid time off - take the time that you need Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents Flex spending accounts & company-provided group term life & disability Subsidized lunch via Forkable on days worked from our office 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, Spring Health & BetterUp Coaching We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities #LI-TC1 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 $270,000 — $350,000 USD

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description We're seeking board-certified Gynecologists to provide comprehensive, empathetic, and collaborative care to women, including diagnosis, treatment, and management of chronic and acute conditions. - Conduct thorough patient assessments and develop personalized treatment plans via video visits - Collaborate with a multidisciplinary team to deliver the highest standards of care - Complete required training and adhere to company policies and best practices - Promote preventative care and overall well-being through education and evidence-based strategies - Maintain accurate and up-to-date patient records - Dedicate a minimum of 10 patient-facing hours per week, including consults, prescribing medications when appropriate, and providing necessary medical guidance - Charting, addressing patient questions, and responding to administrative tasks and messages Qualifications - MD or DO degree from an accredited institution - Active national board certification in Gynecology - Minimum of 2 years of consecutive experience as a Gynecologist specializing in women's health and treating chronic conditions such as PCOS, Endometriosis, Hypothyroidism, Hashimoto’s, Metabolic Syndrome, Menopause, Fertility, Postpartum, PMDD, and Obesity - Ability to operate effectively as an independent provider with strong diagnostic and problem-solving abilities - Exceptional written and verbal communication with a focus on clarity and compassion - Strong ability to connect with patients virtually and provide empathetic care - Dedication to delivering treatments grounded in the latest research - Highly skilled in navigating multiple computer screens and proficient in tools such as EMR, text expanders, Gmail, Google Calendar, Zoom, and scheduling platforms - Experience in telemedicine is a plus! Requirements - An active, unrestricted, and unencumbered professional license in at least one U.S. state is required. - All active and pending state licenses held at the time of application are collected and reviewed. - Hiring decisions are based on current state hiring needs, which may change over time. - Applicants may not move forward if there is no immediate need for their specific license(s). - We often revisit opportunities in the future as hiring needs evolve and when licensure, experience, and other role requirements align. Benefits - Competitive per-visit rates, plus additional pay for charting, administrative tasks, and other patient-related tasks - Fully remote role - work from anywhere in the US - 1099 Contract Agreement - enjoy the flexibility and independence of a contractor role - Flexible schedules - set the hours that best fit your lifestyle and availability - Comprehensive malpractice insurance coverage provided - Join us in transforming healthcare for women, making a meaningful difference every day - Engage with and learn from a network of dedicated Allara providers - Be part of a supportive, diverse, and collaborative team that values innovation and inclusion