Lead statistical programming activities for clinical trials, ensuring high-quality deliverables, analyzing data using SAS or R, and collaborating with cross-functional teams.

Lead clinical data management for Tango's outsourced trials from planning through database lock. Oversee CRO partnerships, data standards (CDASH/SDTM), database design, edit checks, UAT, data quality metrics, vendor oversight, and cross-functional collaboration to ensure timely, high-quality clinical datasets.

The Director, HRBP advises on HR strategies and solutions, talent management, and organizational change within clinical functions to support business objectives.

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.

The Director of Compliance will lead compliance initiatives, develop policies, and provide training, ensuring adherence to healthcare regulations within a biotechnology company.

The Manager of Quality Assurance ensures compliance with GMP regulations for CMC development programs, leads QA activities, reviews documentation, and mentors teams.

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.

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.

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.

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.

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.