{"id":1737557,"url":"https://alion.io/job/bridgebio-pharma-sr-ctmassociate-director-qed-alliance-support","title":"Sr. Clinical Research Associate/Clinical trial Manager","company":{"id":3681,"name":"BridgeBio Pharma","domain":"bridgebiopharma.com","url":"https://alion.io/company/bridgebiopharma","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Greenhouse","truth_index":{"grade":"A","score":90,"open_postings":14,"ghost_share":0,"stale_share":0.214,"repost_share":0,"time_to_fill_p50_days":63,"computed_at":"2026-11-01T06:10:25Z"}},"role":"Biotech","role_family":"Biotech","seniority":"senior","employment_type":null,"work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":145000,"max":177000,"currency":"USD","period":"year","gross":null,"usd_annual":177000},"salary_estimate":null,"experience_years_min":4,"visa_sponsorship":false,"relocation_package":false,"has_equity":true,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false},{"name":"ICH Guidelines","optional":false}],"status":"live","first_seen_at":"2026-10-02T21:10:06Z","employer_posted_date":"2026-10-19","last_verified_at":"2026-11-01T21:46:10Z","board_verified":true,"closed_at":null,"days_open":30,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":30},"description":"Mavericks Wanted \nWhen 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 \nIn 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. \nTogether 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. \nCompany Overview\nBridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines for patients with genetic diseases and cancers with clear genetic drivers. Founded in 2015, the company has built a portfolio of 20+ drug development programs spanning preclinical to late-stage development across multiple therapeutic areas.\nQED Therapeutics, an affiliate of BridgeBio Pharma, is dedicated to developing targeted treatments for FGFR-driven skeletal dysplasia, focusing on Achondroplasia (ACH) and Hypochondroplasia (HCH). Achondroplasia is the most common form of genetically driven short stature, and Hypochondroplasia is a genetic condition that affects the way bones grow; both conditions can lead to significant medical complications throughout life. With our investigational therapeutic candidate, infigratinib, we seek to deliver meaningful treatment options that address the underlying cause of these conditions and improve outcomes for children and families living with ACH and HCH.\nWhat You’ll Do\nAs a Sr. Clinical Research Associate/Clinical Trial Manager, you will collaborate within the Clinical Operations team to support the timely conduct of clinical studies according to protocols, GCP, SOPs, and applicable regulations. You will be responsible for performing quality study oversight processes, including monitoring communications with site staff and clinical vendors, and reviewing monitoring trip reports.\nPartner with the Clinical Operations Study Lead and cross-functional team to support clinical studies from planning and start-up through execution, maintenance, and close-out in accordance with assigned SOPs, ICH/GCP, and corporate and departmental goals.\nLead operational management for assigned regions and sites by driving site initiation activities, monitoring performance metrics, identifying and mitigating risks, driving escalations and action-item closure, and representing regional performance in study team and cross-functional discussions.\nLead aspects of vendor management for the CRO and other key vendors (IRT, imaging, central and specialty labs, etc.), establishing expectations, ensuring deliverables are met, performance measures are maintained, and escalating as needed; address performance gaps and drive corrective actions to closure.\nProvide oversight of CRO monitors by reviewing monitoring documentation, evaluating monitor and site performance, conducting oversight or co-monitoring visits as needed, and identifying cross-site or systemic risks.\nContribute to the development and maintenance of study documents, including informed consent forms, site training materials, CRFs, monitoring plans, source document templates, protocols, investigator brochures, and regulatory submission materials under the direction of the study lead.\nEnsure the Trial Master File is complete, current, accurate, and inspection-ready, and drive resolution of missing or deficient documentation.\nApply ICH E6(R3) Good Clinical Practice principles, including quality by design, risk-proportionate oversight, critical-to-quality factors, participant protection, and reliable trial results, across study activities.\nExercises sound judgment to resolve or, as appropriate, seek expert input on protocol and drug questions, safety, regulatory, and legal questions.\nParticipates in the review and negotiation of site budgets and contracts.\nSupport and participate in Investigator Meetings and other study-related meetings, as required.\nPromote a collaborative, respectful, quality-focused work environment.\nAdditional Clinical Operations activities may be assigned as appropriate.\nTravel as required to carry out responsibilities (up to 20%).\nWhere You'll Work\nThis is a U.S.-based remote role that will require quarterly or as-needed visits to our San Francisco Office.\n Who You Are\nHold a bachelor’s degree or equivalent training and experience (i.e., RN/PA, BSN degree) in a scientific or medical field.\nMinimum 4-6 years of clinical study experience, preferably within biotechnology or pharmaceutical sponsor organization.\nExperience supporting global studies in a fast-paced environment.\nSuccess in working with CROs and vendors; Must have vendor management experience in Clinical Operations.\nExcellent communication skills and ability to achieve milestones in a team environment.\nAbility to communicate and collaborate respectfully in a remote environment.\nAbility to build and maintain strong working relationships within the department, cross-functionally, with clinical sites, vendors, and CROs to meet a project or corporate goal.\nWorking knowledge of ICH E6(R3) Good Clinical Practice principles and risk-based quality management.\nExperience using M.S. Office Suite (Excel, Word, PowerPoint) and SmartSheet\nAt 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.\nSalary\n$145,000—$177,000 USD\nAs 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.\nFor BridgeBio Full-Time U.S Based Roles:\nFinancial & Rewards \nMarket-leading compensation \n 401(k) with employer match \n Employee Stock Purchase Program (ESPP) \n Pre-tax commuter benefits (transit and parking) \nReferral bonus for hired candidates \nSubsidized lunch and parking on in-office days \nHealth & Well-Being \n100% employer-paid medical, dental, and vision premiums for you and your dependents \n Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA) \nFertility & family-forming benefits \n Expanded mental health support (therapy and coaching resources) \nHybrid work model with flexibility \nFlexible, “take-what-you-need” paid time off and company-paid holidays \nComprehensive paid medical and parental leave to care for yourself and your family \nSkill Development & Career Paths: \nPeople 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 \nWe provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching \nWe celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities \nBy applying, you acknowledge that BridgeBio will process your personal information as described in our Global Candidate Privacy Notice. 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