Ideaya Biosciences - San Diego, CA

posted about 2 months ago

Full-time - Senior
Remote - San Diego, CA
Professional, Scientific, and Technical Services

About the position

IDEAYA Biosciences is seeking an experienced, motivated, and outgoing Clinical Scientist for the position of Director/Senior Director, based in either South San Francisco or San Diego. This role is pivotal in providing medico-scientific expertise to one or more clinical projects, working closely with the clinical leader. The successful candidate will be required to be onsite four days per week, in accordance with company policy, and local candidates are preferred. In this role, typical activities will include writing clinical development concepts and plans for molecules at all stages of development, drafting protocol synopses, protocols, and protocol amendments. The Director/Senior Director will also be responsible for writing and reviewing informed consent forms, partnering with Clinical Operations on site selection and communication, and updating clinical sections of investigator brochures. Additionally, the role involves representing the medical function on clinical study teams, reviewing and interpreting safety data, and assisting in the creation of clinical study reports and publications. The candidate will also be involved in training colleagues and study site staff, organizing opinion leader advisory boards, and supporting Health Authority interactions. The Director/Senior Director will participate in both study-level and program-level activities, including authoring safety and efficacy summaries, clinical overviews, and risk management plans. This position requires a strong background in clinical oncology, with at least two years of industry experience in oncology and previous participation in clinical development programs. The ideal candidate will possess excellent communication skills, the ability to adapt to a fast-paced environment, and a commitment to working collaboratively within a project team structure. The successful candidate will thrive in a mentored environment, taking responsibility for assigned activities while functioning largely independently. They will be comfortable presenting data to peers and senior management, and will embrace the challenges and opportunities of working in a small company environment.

Responsibilities

  • Writing clinical development concepts and plans for molecules at all stages of development
  • Drafting protocol synopses, protocols, and protocol amendments
  • Writing and reviewing informed consent forms
  • Partnering with Clinical Operations on site selection and communication
  • Updating clinical sections of investigator brochures
  • Representing the medical function on clinical study teams
  • Reviewing and interpreting safety data and serious adverse events
  • Assisting in the creation of clinical study reports and publications
  • Training colleagues and study site staff on therapeutic areas and protocols
  • Organizing and participating in opinion leader advisory boards
  • Conducting therapeutic area research and competitor analysis
  • Supporting Health Authority interactions and submissions
  • Presenting study results to internal and external committees
  • Participating in program-level activities including authoring safety and efficacy summaries and clinical overviews

Requirements

  • Bachelor's degree with strong knowledge of clinical oncology
  • At least 2 years of industry experience in oncology
  • Previous participation in a clinical development program
  • Experience in clinical trials with small molecules preferred
  • Skilled in protocol design, interpretation, and medical monitoring
  • Experience in assessment of adverse events and patient safety
  • Knowledge of Good Clinical Practice
  • Excellent written and oral communication skills
  • Capacity to adapt to a fast-paced and changing environment
  • Fluency in English is required

Nice-to-haves

  • Training and experience in immuno-oncology
  • Postgraduate qualification in clinical oncology (e.g., Master's degree)
  • MD, Nurse Practitioner's License, PharmD or PhD
  • Background in closely related functions (e.g., clinical operations, regulatory affairs, biometrics)

Benefits

  • Medical, dental, and vision coverage (100% company paid for employees and 90% for dependents)
  • Retirement benefits
  • Employee Stock Purchase Plan (ESPP)
  • Wellness programs
  • Annual bonus eligibility
  • Equity refresh eligibility
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