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Clinical Trial Manager, Oncology

6-8 years
$130,000 – $142,500
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 Manager, 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: $130,000 – $142,500 (plus bonus & equity)


About the Company

Eikon Therapeutics is a pioneering biotech company utilizing Nobel Prize-winning innovations in live-cell imaging to discover new treatments by unlocking previously inaccessible drug targets.


Role Summary

As a Clinical Trial Manager (CTM) within the Oncology Clinical Operations team, you will lead the day-to-day planning and execution of international clinical studies. You’ll ensure operational excellence, data quality, and regulatory compliance across study phases while working cross-functionally in a fast-paced environment focused on advancing cancer treatment.


Key Responsibilities

  • Oversee in-house management of international oncology clinical trials

  • Develop operational plans for trial implementation and execution

  • Collaborate with internal and external stakeholders (e.g., clinical scientists, regulatory, CROs, vendors)

  • Manage trial start-up, site selection, documentation, monitoring, and closeout activities

  • Ensure study compliance with ICH-GCP, FDA, and global regulatory standards

  • Identify risks and deviations; implement mitigation strategies

  • Maintain and review Trial Master File (TMF) and related documentation

  • Contribute to the development of study documents including protocols, CRFs, and SOPs

  • Support patient recruitment, site engagement, and retention strategies


Qualifications

  • PhD + 3 years | Master's + 6 years | Bachelor's + 8 years in life sciences or healthcare

  • Proven experience managing oncology trials from start-up to closeout

  • Strong understanding of ICH-GCP, FDA regulations, and oncology research

  • Expertise in project management, budgeting, and cross-functional collaboration

  • Skilled in using Veeva CTMS and understanding of oncology medical terminology

  • Strong analytical, organizational, and communication skills


Compensation & Benefits

  • Competitive base salary, performance bonus, and equity

  • 401(k) plan with company match

  • 95% employer-paid medical, 100% dental and vision insurance

  • Mental health and wellness benefits

  • Weeklong summer and winter shutdowns

  • Generous PTO and holiday leave

  • Fully covered life and AD&D insurance, plus supplemental options

  • Daily subsidized lunch for onsite employees

  • Enhanced parental leave policy


Diversity & Inclusion

Eikon Therapeutics is an equal opportunity employer and values diversity in all forms.