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Associate Director, Clinical Scientist - Oncology

10+ years
$189,000 – $206,150
10 May 5, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Associate Director, Clinical Scientist – Oncology

Company: Eikon Therapeutics
Location: Millbrae, CA; New York, NY; Jersey City, NJ (Hybrid – minimum 3 days onsite/week)


Job Type: Full-time

Salary Range: $189,000 – $206,150 (plus bonus & equity)


About the Company

Eikon Therapeutics leverages a revolutionary platform that combines advanced chemistry, biology, computation, and engineering to develop treatments targeting previously undruggable proteins, based on Nobel Prize-winning innovations in molecular microscopy.


Role Summary

The Associate Director, Clinical Scientist – Oncology will lead the scientific and operational aspects of oncology clinical trials. As part of a cross-functional development team, you will play a key role in protocol design, data analysis, medical monitoring, and regulatory documentation to support the development of transformative cancer therapies.


Key Responsibilities

  • Serve as the lead clinical scientist on oncology trial teams

  • Collaborate on protocol design, informed consent forms, and CRFs

  • Support medical monitoring, including data review and deviation analysis

  • Partner with Clinical Operations to ensure execution of study deliverables

  • Guide cross-functional teams in data quality, completeness, and integrity

  • Prepare and contribute to scientific publications, abstracts, and presentations

  • Apply analytical thinking to assess risks and propose mitigation strategies

  • Promote best practices for clinical data review and scientific documentation

  • Provide scientific mentorship to junior team members


Qualifications

  • Bachelor’s degree with 10+ years, or advanced degree (PhD, PharmD, RN) with 8+ years in clinical development

  • Strong understanding of oncology trials, GCP, and ICH guidelines

  • Demonstrated ability to synthesize clinical data into actionable insights

  • Skilled in authoring regulatory documents and study-related materials

  • Capable of cross-functional leadership and effective communication

  • Excellent time management, critical thinking, and decision-making skills

  • Experience in biotech or pharma settings is highly preferred


Compensation & Benefits

  • Competitive salary, bonus, and equity

  • 401(k) plan with company match

  • Medical, dental, and vision insurance (95–100% employer-paid)

  • Mental health and wellness benefits

  • Generous PTO and paid holidays

  • Paid parental leave

  • Life and AD&D insurance

  • On-site lunch subsidies

  • Weeklong shutdowns in summer and winter


Diversity & Inclusion

Eikon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration regardless of background, and reasonable accommodations are available upon request.