About The Position

Hexagon Bio is a venture-backed biotechnology company advancing novel payloads for next-generation oncology ADCs. With its world-class research team, Hexagon Bio has the deep expertise to enable first-in-class ADCs with novel payloads for cancers with high unmet need, with the goal of overcoming resistance and improving tolerability. By combining innovative payloads, optimized targeted delivery, and rational combinations, Hexagon Bio is propelling transformative ADC therapies aimed at delivering deep and durable responses, including in patients whose tumors have developed resistance to existing ADC therapies. Position Summary: Hexagon is seeking a motivated and analytical Clinical Scientist to join our team. This role will focus on providing clinical scientific expertise and data analysis for our lead ADC programs. Reporting to the Head of Clinical/CMO, the Clinical Scientist will support clinical trial design, contribute to study-related documentation development and execution, and perform detailed medical and scientific data reviews on clinical data for internal and safety review committee reviews. This individual will work cross-functionally to support the execution of clinical trials and the translation of platform discoveries into clinical proof-of-concept.

Requirements

  • PhD, PharmD or equivalent advanced degree in a relevant scientific field is desirable (e.g., Biology, Pharmacology, Immunology, or related discipline).
  • 7+ years of industry experience in clinical development overseeing clinical study execution, with a focus on oncology.
  • Proven ability to analyze and interpret complex clinical data to drive scientific insights.
  • Solid understanding of clinical trial design, GCP/ICH guidelines, and regulatory documentation requirements.
  • Strong communication and collaborative skills, with the ability to work effectively in a cross-functional team environment.
  • Experience in fast-paced, high-growth biotechnology environments.
  • Passion for innovation in drug discovery and a collaborative, entrepreneurial spirit.

Responsibilities

  • Contribute to the development of clinical study protocols, investigator brochures, informed consents, and other key study documents.
  • Perform clinical data review and analysis to support study-level decision-making and safety monitoring.
  • Support the preparation of clinical sections for regulatory submissions, including INDs and clinical study reports.
  • Collaborate cross-functionally with Translational Research, Clinical Operations, and Biometrics to ensure scientific alignment across programs.
  • Assist in the medical monitoring process and clinical trial execution in accordance with GCP/ICH guidelines.

Benefits

  • A flexible and dynamic work environment where you pave your own path, Hexagon cultivates employees' unique strengths at all levels and provides mobility across departments.
  • Access to scientific conferences throughout the year.
  • A range of amenities, courtesy of the Menlo Park Labs business park, including shuttle, gym, rock-climbing wall, pool, sauna, sports courts, cafe, bike lockers, and free EV charging stations.
  • Opportunities to engage with the Hexagon community through team-building events like our Hexagon Happy Hours and holiday parties.

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What This Job Offers

Job Type

Full-time

Career Level

Senior

Education Level

Ph.D. or professional degree

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