Senior Director, Head of Feasibility, Americas

Reposted Yesterday
Be an Early Applicant
Hiring Remotely in US
Remote
202K-272K Annually
Senior level
Biotech
The Role
The Senior Director, Head of Feasibility will lead feasibility activities, site identification and recruitment, and manage cross-functional collaborations for clinical trials. Responsibilities include strategic data analysis for study planning and risk mitigation, overseeing recruitment programs, and ensuring alignment with commercial and regulatory objectives.
Summary Generated by Built In

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

As the Regional Strategic Feasibility Lead within Global Clinical Operations (GCO), you will play a vital role in collaboration with the global strategic feasibility lead, study teams, and cross-functional stakeholders in the region to deliver data-driven strategic feasibility reports for early to late-stage medicines development. Your responsibilities will encompass site identification and recruitment and retention recommendations, ensuring the successful execution of clinical trials from concept to completion. 

Essential Functions of the job:

Strategic Liaison and Cross-functional Coordination

  • Act as the primary point of contact for the Global Strategic Feasibility and Regional Clinical Operations teams for Feasibility and Re-Feasibility activities. 
  • Liaise cross-functionally to expedite and predictively deliver feasibility insights at various levels (TA, indication, program, study), ensuring standardization of data, tools, and processes for quality decision-making. 

Data-driven Feasibility Recommendations: 

  • Combine and integrate data from internal stakeholders and external sources to provide clear feasibility strategies for site identification, recruitment, and retention at the TA/indication/program level. 
  • Utilize comprehensive data analysis, including local treatment standard of care, disease prevalence, drug landscape, and historical trial data, to inform protocol development and establish geographic footprints and proposed sites for participation in clinical studies. 
  • Consider the unique needs of each indication, patient population, study, and business priorities. 

Enrollment Forecasting and Risk Mitigation: 

  • Utilize competitive intelligence data to develop accurate study startup forecasts, benchmark assumptions, and enrollment plans. 
  • Maintain patient enrollment forecasts strategically, adjusting for new influencing factors and developing risk mitigation plans. 
  • Lead the design and implementation of study-specific recruitment programs, collaborating with study teams, vendors, and CROs as needed to optimize participant recruitment. 

Continuous Improvement and Innovation: 

  • Implement creative processes, methodologies, data, and technologies to enhance the delivery of Feasibility and Study Startup Services. 
  • Contribute to ongoing strategic planning, capability assessments, and training efforts to ensure successful feasibility support. 
  • Stay up to date with current therapeutic area knowledge, assessing its impact on operational strategies. 
  • Perform root cause analysis and develop mitigation strategies to address study execution and enrollment challenges. 
  • Participate in regional and global projects, representing Clinical Operations and Study Optimization to support BeiGene R&D goals. 

Supervisory Responsibilities:  

  • Drive high level of ownership and accountability within team and with external stakeholders 
  • Line Manage - Country Feasibility and Clinical Trial Diversity teams

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

Other Qualifications:    

  • Experience with trial optimization vendors, tools, and methods. 
  • Proficiency with software models and database structures. 
  • Expertise in principles driving country/site identification, feasibility, and study startup strategies. 
  • Validated experience in data analysis, data interpretation to drive inform decision making. 
  • Tried experience in managing, influencing, building, and managing relationships and achieving results with senior partners in conflicting priority environment. 
  • 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 12 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: $202,200.00 - $272,200.00 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.

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact [email protected].

Top Skills

Analytic Tools (Citeline
Ctms Applications
Edc Applications
Microsoft Office Suite
Trialtrove)
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The Company
HQ: Cambridge, MA
2,862 Employees
Year Founded: 2010

What We Do

BeiGene is a global biotechnology company that is developing and commercializing innovative and affordable oncology medicines to improve treatment outcomes and access for far more patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 8,500 colleagues spans five continents, with administrative offices in Beijing, China; Cambridge, U.S.; and Basel, Switzerland. To learn more about BeiGene, please visit www.beigene.com and follow us on Twitter at @BeiGeneGlobal.
See our community guidelines: bit.ly/39o3O6j

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