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Clinical Trial Associate, Oncology

2+ years
$104,000 – $114,000,
10 May 5, 2025
Job Description
Job Type: Full Time 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
Locations: Millbrae, CA; Jersey City, NJ; New York, NY


Company Overview

Eikon Therapeutics is a biopharmaceutical company using revolutionary technology across chemistry, engineering, computation, and biology to develop treatments for life-threatening diseases. The company's platform stems from Nobel Prize-winning research (2014) and enables molecular-level, real-time visualization of protein movement in live cells.


Role Summary

As a Clinical Trial Associate (CTA) in the Oncology department, you will support Phase I–III global clinical studies by assisting in planning, coordination, and documentation. The role requires working onsite at least 3 days a week at one of Eikon’s office locations to foster collaboration and operational excellence.


Key Responsibilities

  • Prepare and maintain essential study documents (protocols, informed consent forms, CRFs, etc.)

  • Support study start-up activities including site selection and IRB/ethics submissions

  • Assist in planning investigator meetings and study initiation activities

  • Track investigational product and study material distribution/reconciliation

  • Help resolve data queries and ensure data quality in EDC systems

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

  • Communicate study updates with investigators and site personnel

  • Monitor enrollment and recruitment progress

  • Coordinate monitoring visits and support monitoring activities

  • Stay informed of clinical regulations and oncology trial best practices


Qualifications

  • Education:

    • Advanced degree (no experience required) or

    • Bachelor’s degree + 2 years of relevant experience (life sciences or related)

  • Preferred:

    • Multilingual capabilities (especially in European languages)

    • Previous experience as a CTA, Study Coordinator, or similar role in pharma/biotech/CRO

    • Familiarity with ICH-GCP, FDA requirements

  • Skills:

    • Proficiency in CTMS and EDC systems

    • Strong organization and attention to detail

    • Excellent communication and interpersonal skills

    • Proficient in Microsoft Office

    • Adaptability to new technologies and workflows


Compensation & Benefits

  • Salary range: $104,000 – $114,000, depending on experience

  • Bonus and equity compensation

  • 401k with company match

  • Health insurance: medical (95% paid), dental & vision (100% paid)

  • Mental health and wellness programs

  • Weeklong paid summer and winter shutdowns

  • Paid time off, holidays, enhanced parental leave

  • Daily subsidized lunch (on-site)

  • 100% covered Life/AD&D Insurance, with optional extras