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Clinical Trial Associate, Oncology

2+ years
$104,000 – $114,000
10 May 5, 2025
Job Description
Job Type: Hybrid 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: Clinical Trial Associate, Oncology

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


Job Type: Full-time

Salary Range: $104,000 – $114,000 (plus bonus & equity)


About the Company

Eikon Therapeutics is a cutting-edge biopharmaceutical company harnessing revolutionary microscopy technologies to visualize protein behavior in real-time and develop therapies for life-threatening diseases. Founded by Nobel Prize-winning scientists, Eikon operates at the intersection of biology, computation, engineering, and chemistry.


Role Summary

As a Clinical Trial Associate (CTA) supporting oncology trials at Eikon, you will provide essential support in the planning, coordination, and operational execution of Phase I–III clinical studies. This hands-on role offers an opportunity to directly impact the success of oncology programs by ensuring clinical operations are efficiently managed and compliant with regulatory standards.


Key Responsibilities

  • Support preparation and maintenance of study materials (protocols, ICFs, CRFs, etc.)

  • Assist with site selection, feasibility, and regulatory submissions

  • Organize investigator meetings and study initiation activities

  • Track and coordinate distribution and reconciliation of clinical trial materials

  • Review and help resolve data queries within EDC systems

  • Maintain the Trial Master File (TMF) in collaboration with TMF Operations

  • Facilitate communication among stakeholders (sites, sponsors, internal teams)

  • Monitor study progress including enrollment metrics and timelines

  • Help coordinate and support site monitoring visits

  • Stay up to date with evolving clinical trial regulations and oncology-specific best practices


Qualifications

  • Bachelor’s degree with 2+ years of experience in clinical research or an advanced degree with relevant coursework

  • Prior experience as a CTA, Study Coordinator, or within a CRO/pharma setting is preferred

  • Familiarity with ICH-GCP, FDA guidelines, and clinical research best practices

  • Proficiency with CTMS, EDC systems, and Microsoft Office Suite

  • Strong attention to detail, time management, and multitasking abilities

  • Excellent communication and interpersonal skills

  • Knowledge of European languages is a plus


Compensation & Benefits

  • Competitive salary, bonus, and equity package

  • 401(k) with company match

  • Premium-covered health (95%+), dental, and vision insurance

  • Mental health and wellness benefits

  • Weeklong shutdowns in summer and winter

  • Generous PTO and paid holidays

  • Paid parental leave

  • Company-subsidized lunches on-site

  • Life and AD&D insurance


Diversity & Inclusion

Eikon is an equal opportunity employer that values diversity and inclusion in the workplace. All qualified applicants are encouraged to apply.