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HanchorBio Inc

Medical Director (US)

Job Title:

Medical Director


Location: US

Job Responsibilities

  • Develop, execute and maintain clinical development plans (biologics) including Phase 1 through 3, lifecycle management, medical affairs, safety responsibilities, scientific interactions with regulatory bodies with strategy and direction; ensure CDPs are executed on time and within budget
  • Oversee tactical development of clinical trial programs, including literature reviews, clinical CRO/investigator selection, protocol development, clinical operation, interpretation of clinical data, and proactive detection of operational issues; resolve operational issues including protocol amendments
  • Identify strategic issues for therapeutic indications under investigation; keep abreast of critical evolution of therapeutic options for chosen therapeutic indications and alert Senior Management and clinical operation staff to evolve management paradigms
  • Orchestrate and manage clinical aspects of regulatory strategies and interactions with regulatory agencies; review and approve all correspondence to regulatory agencies as appropriate; review submissions to Ethics Committees, input into responses to any questions/issues raised and support of operational teams
  • Interact with KOLs, MSLs and corporate partner(s) and investors
  • Ensure that company practices are compliant with relevant drug regulations
  • Build, grow and manage a high-functioning clinical organization with a focus on staff development, clinical quality, and appropriate succession planning

Job Requirements

  • MD degree with 10+ years’ experience in clinical practice treating patients or biotech/pharmaceutical industry experience as a Sponsor working on investigational new drugs.
  • Experience with, or strong knowledge of oncology drug development. Experience in clinical pharmacology and early-stage clinical development is desirable.
  • Excellent knowledge of the competitive environment for drugs in the oncology marketplace and in research and development pipelines.
  • Comprehensive knowledge of clinical research concepts, practices, and GCP and ICH Guidelines.
  • Able to read, write and speak English and possess excellent written and oral communication, collaboration and “think-out-of-the box” problem-solving skills and will be capable of articulating company clinical and regulatory strategies.
  • Must have a results-oriented work ethic, a positive attitude, reliable team player with strong sense of responsibility.
  • Comfortable meeting deadline in a fast-paced biotech environment



please visit:


October 18, 2023


United States

International Employee

Sponsor H1b

Sponsor O1

Working Style





Upcoming Conference

Nov. 12th, 2022

BioPacific Conf.

The BioPacific Conference is the annual flagship event of the CABS. Our mission is to bring scientists, executives, and bio-pharmaceutical professionals from the Pacific Rim countries together to discuss the latest advances in the world of life sciences, the unprecedented challenges and promises facing the industry, and the breath-taking developments and opportunities in Asia/Pacific countries

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