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The Senior Manager will lead statistical programming for clinical trials, ensuring timely, compliant deliverables and collaboration with cross-functional teams in oncology.
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Lead the biostatistics function for clinical trials in oncology, overseeing statistical deliverables, guiding teams, and ensuring regulatory compliance.
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The Director, HRBP advises on HR strategies and solutions, talent management, and organizational change within clinical functions to support business objectives.
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The Director of Biostatistics leads the statistical aspects of clinical programs, collaborates with CROs, and oversees regulatory submissions, ensuring effective trial designs and statistical analysis.
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The Director of Compliance will lead compliance initiatives, develop policies, and provide training, ensuring adherence to healthcare regulations within a biotechnology company.
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The Manager of Quality Assurance ensures compliance with GMP regulations for CMC development programs, leads QA activities, reviews documentation, and mentors teams.
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The Associate Director, Corporate Counsel supports corporate governance and public reporting obligations, provides strategic legal guidance, manages SEC filings, and collaborates with senior executives and internal teams.
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Manage global clinical trials from start to finish, coordinating with cross-functional teams, ensuring on-time and on-budget performance, and overseeing project timelines and risks.
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Lead scientific, technical, and operational Pharmaceutical Sciences (DMPK, preclinical safety, clinical pharmacology) to support IND/NDA submissions. Build and mentor teams, collaborate across discovery and development, optimize study design, and liaise with CROs and regulatory authorities.
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Lead global Phase 3 clinical development for PRMT5 program (TNG462), drive protocol design and regulatory strategy, manage clinical scientists, coordinate cross-functional teams, support regulatory filings and publications, and engage external investigators and partners.
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Lead the pharmacovigilance team and oversee safety science strategies for oncology programs, manage interactions with health authorities, and mentor professionals in a high-performing safety organization.






