BeiGene, Ltd.

Executive Director, Clinical Development, Breast Cancer

BeiGene, Ltd.$329K — $409K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 8+ years of experience, preferably 10+ in biotech/pharmaceutical or relevant academic settings
  • Advanced degree (MD or MD equivalent) with specialization in hematology/oncology
  • Expertise in complex scientific knowledge and drug translation
  • Strong scientific and team communication abilities
  • Experience managing clinical trials from start to completion

Responsibilities

  • Lead clinical development strategy planning and presentations for governance committees
  • Provide leadership and oversight for assigned clinical studies and programs
  • Collaborate with regulatory partners on filings and documents
  • Offer clinical input to regulatory submissions processes
  • Develop and implement communication strategies for studies including KOL interactions
  • Adapt clinical strategies based on competitive landscape insights
  • Identify resource needs and guide career development for team members

Benefits

  • Comprehensive medical, dental, and vision insurance
  • 401(k) plan with employer matching
  • Flexible spending accounts (FSA/HSA)
  • Life insurance coverage
  • Generous paid time off (PTO)
  • Wellness programs
  • Equity opportunities through stock option plans
Full Job Description
The Executive Director, Clinical Development will effectively lead BeOne clinical assets through successful development of early and late phase clinical development strategies and deliverables in partnership with multiple functions across the organization, and with external academicians and collaboration partners. The candidate will report to the Vice President, Clinical Development, Breast and Women's Cancers Franchise.

As a leader in the organization, the incumbent will be involved with asset and disease strategy and help assure that activities are executed within expected scope, budget, and timelines. The incumbent will play a key role in the establishment and growth of Clinical Development team as a Global Clinical Development Team Leader. This leader must be a thoughtful and mentoring manager, responsible for hiring, training, developing, and retaining talent.

Specifically, the incumbent will collaborate with a variety of internal and external partners and stakeholders, such as clinical investigators, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in Clinical Development, research, business development, commercial operations, legal, translational science etc.

Key Roles & Responsibilities:
  • Key contributor in Clinical Development strategy planning and leading presentations to various internal governance committees
  • Provides leadership and clinical oversight across all assigned studies and programs, and has direct accountabilities to assigned clinical programs
  • Works with regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation
  • Support other functions and teams with clinical science information and input for regulatory submissions and other regulatory processes
  • Play a lead role in the development and implementation of communications strategies to support existing and completed studies including KOL interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials
  • Contribute clinical science input into the relevant therapeutic/disease area scientific strategy
  • Understands competitive clinical development landscape and adjusts strategy accordingly
  • Identifies strategic and incremental organizational resource needs re: People, Process and Technology
  • Plan and direct career development for US clinical development team members
  • Models values and Leadership Expectations, provide strong mentoring and coaching skills for team members


Qualifications:

  • Minimum 8+ years of experience, 10+ preferred within other biotech/pharmaceutical or relevant academic credentials companies
  • Advanced degree (MD or MD equivalent) with subspecialty training in hematology/oncology


Requires complex scientific knowledge and development expertise to translate an asset into a medicine
  • Able to facilitate and integrate strong science into commercially viable products
  • Effective scientific and team communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills
  • Experience in managing study start-up, directing and guiding study team execution, data cleaning, medical review, database locks, managing health authority responses are also required


Program Management and Clinical Development Expertise
  • Identifies the need for and leads the team in developing strategies to achieve team objectives
  • Leads the team in leveraging all available resources and information to maximize the effectiveness of long- and short-range planning
  • Having direct accountability for driving clinical development programs and enjoy the accountability of working in a fast-paced, entrepreneurial environment


Team Leadership and Credibility
  • Able to build highly productive teams both cross-functionally and externally
  • Able to develop high potential team members into leadership positions
  • Develop strong cross-functional working relationships with a diverse team of senior leaders


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: $329,700.00 - $409,700.00 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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