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Associate Director, Clinical Trial Diversity, Clinical Operations

Job in Myrtle Point, Coos County, Oregon, 97458, USA
Listing for: BeiGene
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 190500 USD Yearly USD 190500.00 YEAR
Job Description & How to Apply Below
Location: Myrtle Point

Why Consider this Job Opportunity

- Salary up to $190,500 annually

- Opportunity for career advancement and growth within the organization

- Comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness programs

- Potential for annual bonuses and participation in an incentive compensation plan

- Chance to make a meaningful impact on cancer research and patient accessibility

- Opportunity to work with cross‑functional teams in a collaborative environment

What to Expect (Job Responsibilities)
  • Operationalize the clinical trial diversity strategy through data‑driven insights and outreach models
  • Collaborate with Clinical Operations, Regulatory, and other corporate functions to enhance diversity in study design and site selection
  • Aggregate and analyze real‑world data to inform enrollment targets and ensure representative patient populations
  • Build and maintain relationships with investigational sites and community partners to support patient recruitment
  • Represent the employer at scientific meetings and community forums to promote patient‑centered research initiatives
What is Required (Qualifications)
  • Bachelor’s degree required; graduate degree preferred (MBA, MSc, PhD, MD, and/or MPH)
  • Minimum 8 years of relevant clinical research experience
  • Strong understanding of FDA Diversity Action Plan requirements and ability to translate them into operational metrics
  • Proven ability to work independently and manage competing deadlines
  • Strong leadership, organizational, interpersonal, and communication skills
How to Stand Out (Preferred Qualifications)
  • Experience with clinical data warehouses and regulatory data reporting
  • Knowledge of public health issues and a commitment to improving cancer medicine accessibility
  • Previous work in the global pharmaceutical industry or clinical trials, particularly in oncology
  • Ability to effectively present to senior leadership and manage external engagement initiatives
  • Strong understanding of the clinical trial process and pharmaceutical product profiles

#Pharmaceutical Research #Clinical Trials #Diversity In Research  #Cancer Research #Career Opportunity

"We prioritize candidate privacy and champion equal‑opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position.

Our role in this specific opportunity is to connect outstanding candidates with a top‑tier employer."

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Position Requirements
10+ Years work experience
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