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Clinical Research Scientist - Breast Cancer Franchise

Job in Coos Bay, Coos County, Oregon, 97458, USA
Listing for: Eli Lilly and
Full Time position
Listed on 2026-01-01
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 308000 USD Yearly USD 308000.00 YEAR
Job Description & How to Apply Below

Employer Industry: Healthcare

Why consider this job opportunity
  • Salary up to $308,000
  • Opportunity for company bonuses based on individual and company performance
  • Comprehensive benefits package including medical, dental, vision, and 401(k) participation
  • Chance to lead and mentor a team of junior scientists while advancing innovative breast cancer therapies
  • Supportive and inclusive work environment with employee resource groups
  • Engage in meaningful work that contributes to improving patient outcomes globally
What to Expect (Job Responsibilities)
  • Contribute to the development and execution of clinical strategies for breast cancer programs while ensuring compliance with regulatory standards
  • Lead the completion of clinical trial documents including protocols, amendments, and clinical study reports
  • Supervise medical monitoring activities, including data review and safety assessments
  • Collaborate with cross‑functional teams to ensure scientific integrity and operational excellence
  • Support regulatory submissions and prepare materials for health authority interactions
What is Required (Qualifications)
  • PhD with 3+ years of industry experience or BS Degree with 10+ years of industry experience in a health‑related field
  • 3+ years of clinical research scientist or clinical trial experience
  • Direct line leadership experience
  • Proven ability to influence others and build a positive working environment
  • Fluent in English with strong written and verbal communication skills
How to Stand Out (Preferred Qualifications)
  • Knowledge or experience in breast cancer disease state
  • Advanced health/medical/scientific graduate degree (e.g., Pharm

    D, MSN)
  • Experience with all phases of a trial lifecycle from design to regulatory submission
  • Strong interpersonal, teamwork, and negotiation skills
  • Willingness to travel domestically and internationally as needed
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