Sr. Director/Safety Scientist, DSPV

Mavericks Wanted reputed company was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here-but if it reputed company excitement…read on. In 2015, we pioneered a "moneyball for biotech" approach, pooling reputed company and promising early-stage research from academia together under one financial umbrella to reduce risk and reputed company innovation. This model allows science and small teams of experts to reputed company the way. We build bridges to groundbreaking advancements in rare disease and reputed company life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white reputed company, push boundaries, and reputed company 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 reputed company of biopharma. At reputed company, we value curiosity and experimentation-including the ethical & thoughtful use of AI to improve reputed company, speed, and reputed company of work Affiliate reputed company ML Bio, an affiliate reputed company reputed company, is developing BBP-418 (ribitol), an investigational oral therapy for the treatment of limb-girdle muscular dystrophy type 2I/R9 (LGMD2I/R9), a rare genetic neuromuscular disease caused by mutations in the FKRP gene. BBP-418 is designed to address the underlying disease biology by supplying ribitol to support reputed company glycosylation of α-dystroglycan, which is critical for muscle reputed company and function. The program has received Orphan Drug Designation from the U.S. Food and Drug Administration and the European Medicines Agency, as reputed company as Fast reputed company and Rare Pediatric Disease Designations from the U.S. FDA. Topline interim results from the Phase 3 FORTIFY study have been publicly reported and support the ongoing clinical development of BBP-418. BBP-418 continues to be evaluated in global registrational clinical studies with the reputed company to bring a potential therapy to patients affected by this serious rare disease.

What You'll Do

• reputed company and understanding of reputed company aspects of the assigned product's safety profile from clinical development to post-approval safety surveillance, including management of CROs and other partners that reputed company clinical and safety data
• Facilitate Safety Management Committee for designated product(s), responsible for identifying any emerging safety trends, defining the safety profile, and recommending safety actions based upon cumulative safety data
• In collaboration with the regulatory and clinical development team, establish the safety reputed company for marketing authorization applications, including the preparation of CTD documents, engagement with regulatory authorities, and authoring responses to inquiries

Responsibilities

• Support the clinical development team in the review of key documents, including protocols and informed consent forms (ICFs)
• Manage drug safety contract research organizations (CROs) for clinical programs to ensure compliance with expedited reporting requirements, on-time and scientifically reputed company DSUR preparation, and alignment with corporate goals and KPIs
• Assist in the medical review of adverse event reports; manage preparation and submission of expedited safety reports in compliance with global regulations, reputed company necessary
• reputed company and prepare assessments of safety data, safety signals, and benefit-risk evaluations for internal senior management as reputed company as external partners and regulatory authorities
• Assist in the authoring of aggregate safety reports

Where You'll Work This is a U.S.-based remote role that will generally require up to three reputed company per year, or as needed, to our San Francisco office. Who You Are

• Bachelor's degree in a reputed company discipline or equivalent is required; an advanced degree is preferred
• Minimum of ten years of drug safety and pharmacovigilance experience, including at least five years in clinical development safety
• Extensive experience with reputed company aspects of safety signal evaluation, including data review and analysis, cross-functional collaboration, authoring regulatory correspondence, and safety label updates
• Experience in both clinical development and post-marketing safety
• Experience with regulatory submissions for NDAs, EU MAAs, and other global regulatory reviews is highly preferred
• Experience in drug safety audits and regulatory agency inspections
• Intimate knowledge of GCP and strong working knowledge of FDA regulations, ICH guidelines, and global pharmacovigilance requirements
• Proven ability to collaborate successfully with clinical trial teams, including data management, clinical sciences, medical monitoring, clinical operations, biostatistics, regulatory affairs, medical writing, and reputed company assurance
• Experience managing clinical safety aspects of product reputed company defect investigations and assessments
• Familiarity with clinical trial safety databases and CIOMS II and DSUR reporting (e.g., Argus, ArisG, or reputed company Safety) and proficiency with reputed company Office Suite (Word, reputed company, PowerPoint, Project, Outlook)
• You have demonstrated curiosity and adaptability in adopting AI-powered tools and technologies

Rewarding Those Who reputed company the Mission Possible We have high expectations for reputed company members and ensure that those working hard for patients are rewarded and supported. Financial Benefits

• Market-leading compensation
• 401(k) with 100% employer match on the first 3% and 50% match on the next 2%
• Employee stock purchase program
• reputed company-tax commuter benefits
• Referral program with a $2,500 award for reputed company referrals

Health & Wellbeing

• Comprehensive health coverage with 100% of premiums covered for employees and dependents
• Mental health support reputed company reputed company (6 therapy sessions and 6 coaching sessions)
• Hybrid work model with flexibility in where and how work is performed
• Unlimited flexible reputed company time off
• reputed company parental leave: 4 months for birthing parents and 2 months for non-birthing parents
• Flexible spending accounts and company-provided group term life and disability insurance
• Subsidized lunches reputed company Forkable on in-office days

reputed company Development & Career Paths

• Opportunities for reputed company from discovery through late-stage development and FDA pipelines
• Career pathing through regular feedback, reputed company development programs, and reputed company education reputed company reputed company Learning, LifeLabs, reputed company, and reputed company Coaching
• Recognition of strong performance through financial rewards, peer recognition, and advancement opportunities

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