BeiGene, Ltd.

Director, Head of Patient Recruitment and Retention, Americas

BeiGene, Ltd.$171K — $231K *
US-AnywhereRemote in United States
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree (or higher) in a scientific, medical, or healthcare discipline.
  • Minimum of 10 years in Feasibility, Clinical Trial Management, and Operations Management.
  • Demonstrated success in leading enrollment strategies in oncology.
  • Established relationships with patient advocacy organizations and recruitment vendors.
  • Experience in data analysis to drive decision-making.
  • Project and budget management experience.
  • Valid experience working with global teams.

Responsibilities

  • Develop and lead patient recruitment and retention strategies for clinical trials.
  • Tailor strategies based on indication, geography, and patient complexity.
  • Establish enrollment forecasting models.
  • Embed patient-centric principles into trial designs.
  • Oversee multi-channel recruitment and retention execution.
  • Identify and manage recruitment vendors and external partnerships.
  • Implement data-driven improvements in recruitment strategies.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • 401(k) retirement plan with company contributions.
  • Flexible spending accounts (FSA/HSA).
  • Life insurance and wellness programs.
  • Paid time off and holiday leave.
  • Employee Stock Purchase Plan and discretionary equity awards.
Full Job Description
General Description:

As the Head of Patient Recruitment and Retention, Americas within Global Clinical Operations (GCO), you will hold a leadership role responsible for designing and executing strategies to enroll and retain patients in BeOne clinical trials This role works with study teams to ensure trials meet enrollment and long term follow-up milestones, implements and manages recruitment vendor partnerships, and liases with patient advocacy organizations to implement patient-focused approaches.

Essential Functions of the job:

Global Recruitment Strategy:

  • Develop and lead a comprehensive, regionally-aligned patient recruitment and retention strategy designed to support portfolio priorities
  • Ensure strategies are tailored to indication, geography, and patient population complexity
  • Establish forecasting models to predict enrollment timelines and risks
  • Integrate recruitment planning early into study design and feasibility processes


Patient Focused Trial Design:

  • Partner with Clinical, Medical, and Protocol Development teams to embed patient-centric principles into study design
  • Identify and address patient burden factors that impact participation and retention
  • Incorporate patient insights, advocacy input, and real-world evidence into recruitment strategies
  • Promote diversity, equity, and inclusion in clinical trial participation


Recruitment and Retention Execution:

  • Oversee execution of multi-channel recruitment strategies (digital, site-based, community outreach, partnerships)
  • Lead development of retention programs to minimize screen failures and dropout rates
  • Ensure deployment of patient support services (e.g., travel, concierge, education tools)
  • Drive continuous monitoring and optimization of recruitment performance


External Partnerships and Vendor Management:

  • Identify, evaluate, and manage recruitment vendors, digital platforms, and patient engagement partners
  • Establish strategic partnerships with patient advocacy groups, site networks, and community organizations
  • Oversee vendor performance to ensure delivery against enrollment goals and timelines
  • Lead sourcing and adoption of innovative patient recruitment technologies and solutions


Continuous Improvement and Innovation:

  • Implement data-driven decision-making using recruitment analytics, digital campaign metrics, and site performance data
  • Leverage real-world data, epidemiology, and predictive analytics to optimize patient targeting
  • Evaluate emerging trends including decentralized trials, digital engagement tools, and AI-driven recruitment
  • Drive innovation pilots and scale successful approaches


Supervisory Responsibilities:
  • Drive cross-functional governance to support site selection, activation, and enrollment execution
  • Line Manage - Patient Recruitment and Retention team members


Computer Skills: Microsoft Office Suite, CTMS applications, EDC applications, analytic tools (e.g. Citeline, Trialtrove, etc.) and additional feasibility software

Other Qualifications:
  • Demonstrated success leading enrollment strategies across various oncology therapeutic areas
  • Established relationships with patient advocacy organizations and recruitment vendors
  • Validated experience in data analysis, data interpretation to drive informed decision making.
  • Shown experience or willingness to learn how developing study delivery strategies and tactical/operational plans aligned to commercial and regulatory objectives.
  • Clinical trial patient and investigator recruitment experience
  • Validated experience in project and budget management.
  • Confirmed experience working with Global teams.


Travel: Travel might be required as per business need.

Education Required:

Bachelor's degree (or equivalent) or higher in a scientific, medical or healthcare discipline with minimum of 10 years of combined experience in Feasibility, Clinical Trial Management, Personnel Management and Operations Management.

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity


Salary Range: $171,900.00 - $231,900.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

About BeiGene, Ltd.

BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
Learn more about BeiGene, Ltd.
Size
8,300 employees
Market Cap
$22.2 billion
Industry
Net Income
-$1.5 billion
Founded
2010
5 Year Trend
+305.7%
Revenue
$308.8 million
NASDAQ

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