Tamil Medical Interpreter (Remote – Canada) Part Time, Temporary $18.50 hourly. At Kelly, meaningful work is impactful and rewarding. If you are compassionate, detail-oriented, and motivated to bridge language barriers, this opportunity is for you. We are hiring Tamil Medical Interpreters to support critical communication needs across Canada via audio (OPI) and video (VRI) platforms. Role Overview As an interpreter supporting healthcare providers, emergency services, and public service organizations, you may be assigned calls involving sensitive, emotional, or potentially distressing subject matter, such as medical emergencies, violence, criminal matters, or other challenging situations. Due to the nature of this role, some calls may require extended engagement or occur during periods of high call volume. Interpreters are expected to maintain professionalism, composure, accuracy, and confidentiality at all times, delivering services in accordance with company standards and ethical guidelines. Why Join Kelly - Competitive Pay: $18.50/hr upon successful training completion - Paid Training: Three weeks of structured, professional training - Candidate must be located in any of these provinces: British Columbia, Alberta, Saskatchewan, Manitoba, New Brunswick, Nova Scotia, Prince Edward Island, or Newfoundland and Labrador. - Purpose-Driven Role: Every call supports patients, families, and professionals - Vacation & Holiday Pay: Promoting work-life balance - Inclusive Culture: Diverse, collaborative environment Key Responsibilities - Provide real-time interpretation between English and Tamil speakers - Facilitate communication in healthcare, insurance, legal, and financial settings - Maintain confidentiality, professionalism, and cultural sensitivity on every call - Deliver interpretation via audio and video platforms - Participate in training, quality monitoring, and performance improvement initiatives Qualifications - Fluency in English and Tamil (speaking & comprehension) - High school diploma or GED - Minimum 18 years of age and legally authorized to work in Canada - Quiet, distraction-free workspace - Strong listening skills, emotional intelligence, and composure - Commitment to three weeks of full-time paid training VRI/Hybrid Readiness & Performance Expectations - Dedicated personal device for business purposes. Desktop/ Laptop/ Tablets are acceptable. - Functional camera with proper lighting for video calls. - Strong, reliable high-speed Wi-Fi (speed test may be required) - Professional noise cancellation headset (required or willingness to purchase) - Demonstrate punctuality, consistency, and accountability.

Title: Sr. Director, Regulatory Affairs Location: San Francisco - 1800 Owens 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. What You'll Do Lead CMC regulatory strategy and execution across development and post-approval programs, ensuring high-quality submissions aligned with global regulatory requirements. Serve as a strategic Regulatory CMC subject-matter expert and key cross-functional partner, influencing regulatory decision-making and program execution. This role is primarily an individual contributor position with the opportunity to mentor, coach, and potentially manage team members as organizational needs evolve. The ideal candidate brings deep Regulatory CMC expertise, strong cross-functional leadership skills, demonstrated experience with global and ROW filings (e.g., MENA, LATAM, APAC), and practical fluency leveraging AI-enabled and digital tools to improve regulatory workflows and deliverables. Responsibilities - Lead CMC regulatory strategy, planning, and execution for IND/CTA, NDA/MAA, post-approval submissions, and global registrations across development programs - Partner closely with CMC, Quality, Regulatory Operations, and cross-functional stakeholders to ensure timely, high-quality regulatory submissions aligned with global health authority expectations - Provide strategic guidance on CMC regulatory risks, change controls, health authority interactions, and submission strategies to support program objectives and regulatory compliance - Coordinate and review responses to CMC-related health authority requests and ensure regulatory conformance of technical documentation, manufacturing information, validation activities, and labeling content - Mentor and coach junior team members and provide oversight for vendors and/or assigned staff, including prioritization, feedback, and support for development activities - Apply AI-enabled tools and digital technologies to improve the efficiency, quality, and consistency of regulatory deliverables while adhering to company policies and data governance standards - Contribute to global regulatory activities, including demonstrated experience supporting Rest of World (ROW) submissions (e.g., MENA, LATAM, APAC) and coordinating regional filing requirements and strategies 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. Who You Are - BA/BS degree in Chemistry, Pharmaceutical Sciences, Life Sciences, or related scientific discipline required; advanced degree preferred - Extensive Regulatory Affairs CMC experience within the biotechnology and/or pharmaceutical industry, including successful support of NDA/MAA submissions for new chemical entities in pre- and post-approval environments - Demonstrated experience leading complex global regulatory submissions, including Rest of World (ROW) regions (e.g., MENA, LATAM, APAC), with ability to navigate regional regulatory requirements and coordinate cross-regional filing strategies - Strong knowledge of global health authority regulations, CMC development, manufacturing processes, and Quality documentation standards, with the ability to apply regulatory strategy in complex development environments - Proven ability to lead through influence in a matrixed organization, including strong cross-functional collaboration, strategic thinking, project management, communication, and problem-solving skills - Demonstrated experience mentoring, coaching, and developing others; prior direct people management experience preferred but not required - Demonstrated experience utilizing AI-enabled or digital tools to improve efficiency, quality, or decision-making in regulatory or technical workflows while maintaining compliance with company policies and data governance standards - Ability to travel as needed (approximately 10–20%) to support business and regulatory activities 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 $285,000—$320,000 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 - - 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 - 401(k) with employer match

• Processes second level reviews in compliance with Medicare/CMS • Provides appropriate level of care classifications and continued stay reviews in compliance with CMS • Acts as a liaison between the medical staff, utilization review, and 3rd party payers • Reviews the entire claim denial process, including Appeals and Grievances • Serves as a Physician member of the utilization review team

Role Description The Medical Officer and Clinical Informatics Technologist will provide advanced clinical, medical informatics, and health data expertise to support the CMS Innovation Center (CMMI). This role plays a key part in helping CMMI evaluate, design, and improve innovation model tests and health care delivery approaches by leveraging expertise in: - Patient-led data sharing - Remote patient monitoring - Health data standards - Interoperability - Artificial intelligence - Clinical quality analysis The position supports engagements with clinicians, professional medical societies, informaticists, technologists, and additional stakeholders across government and the healthcare ecosystem. Qualifications - Deep expertise in clinical informatics, health data standards, interoperability, and quality assurance - Experience working with AI tools, remote patient monitoring data, and patient-generated health data - Ability to assess complex, vaguely defined problems and develop strategic solutions - Familiarity with CMS/CMMI health system transformation goals - Strong communication skills for cross-disciplinary collaboration - Ability to provide high level clinical interpretation of data, models, and policy proposals Requirements - Doctor of Medicine (M.D.), with a specialty in Pediatrics - 10+ years of relevant professional experience in clinical practice and medical/clinical informatics - Active, unrestricted medical license with State Board Certification in Pediatrics - American Board of Preventive Medicine (ABPM) Certification in Clinical Informatics Benefits - Hourly pay range: $130.00 to $158.00 - Competitive base salary commensurate with qualifications and experience - Comprehensive benefits package, including: - Medical, dental, and vision insurance - 401(k) plan with company matching - Tax-deferred savings options - Supplementary benefits - Paid time off - Professional development opportunities