BeiGene, Ltd.

Senior Project Manager, Clinical Biomarker

BeiGene, Ltd. • $140K — $185K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 7+ years' experience with a Bachelor's or 5+ years with a Master's or 3+ years with an MD/PhD in a biology/medical field.
  • Experience in the pharmaceutical industry or academia is preferred.
  • Strong understanding of scientific concepts and translational research related to oncology biomarker development.
  • At least 7 years of project management experience in a fast-paced environment.
  • Proven organizational and cross-functional project management skills.
  • Excellent verbal and written communication skills in English.
  • Ability to work effectively on multiple oncology programs.

Responsibilities

  • Independently manage biomarker and bio-sample testing activities for clinical trials.
  • Collaborate with internal teams to drive biomarker operational activities and ensure compliance.
  • Provide training to investigator sites on bio-specimen collection and processing.
  • Participate in clinical study team meetings and offer updates on biomarker progress.
  • Ensure alignment of biomarker strategy with device partners and lab vendors.
  • Oversee junior project managers and lead the US biomarker operations team.

Benefits

  • Comprehensive medical, dental, and vision plans.
  • 401(k) with potential employer contributions.
  • Flexible spending accounts for health and dependent care.
  • Paid time off for vacations and wellness.
  • Life insurance benefits.
  • Opportunities for discretionary equity awards and employee stock purchase plan participation.
Full Job Description
General Description:

Manage biomarker related operational work for clinical trials and programs. Act as biomarker operation representative to lead/participate in cross-functional activities and initiatives. Act as key vendor liaison to manage vendor relationship, resolve account level issues and improve processes. Oversee and manage the performance of junior project managers.

Essential Functions of the job:
  • Independently manage biomarker and bio-sample testing activities for clinical trials, including but not limited to review and finalize lab vendors key documents (such as lab manual, lab database design documents, contracts & budget, etc. ) , track bio-specimens, schedule and execute bio-specimen testing based on study needs. Oversee lab vendor performance and act as key vendor liaison to resolve account level issues and improve collaboration and processes.
  • Collaborate and communicate with internal functional stakeholders including biomarker scientists, clinical operations and others, to drive the biomarker related works for clinical trials, such as manage lab vendors timeline, control biomarker budget, ensure compliance and quality, etc. Build collaborative relationships with cross-functional teams as biomarker operation representative and lead/participate cross-functional activities and initiatives.
  • Collaborate with internal teams to review key study documents such as ICF, EDC design specification, IRC integration specification, etc. and provide training to investigator sites as needed for sample collection schedule, sample processing and shipment, etc.
  • Participate in clinical study team meetings and program meetings, providing updates and insights related to biomarker activities and progress.
  • Have a good knowledge of CDx regulations and manage three-way communications with both device partners and lab vendors to make sure biomarker strategy and CDx strategy is implemented. Participate in vendor selection activities at program/platform level and provide insights from operational perspective.
  • Oversee junior project managers' work and performance. Lead US biomarker operation team.


Supervisory Responsibilities:
  • Provide training and coaching to project coordinators, junior project managers
  • Manage project coordinators/junior project managers performance


Computer Skills: Proficient in MS office

Other Qualifications:
  • 7+ years' experience with Bachelor or 5+ years with MS, or 3+ years with MD, PHD in biology/medical major.
  • Experience in the pharmaceutical industry and/or academia is preferred
  • Understanding of scientific concepts and experience in translational research and oncology biomarker development.
  • At least 7 years project management experience
  • Proven organizational and project management skills and the ability to manage cross-functional efforts.
  • Ability to work effectively on multiple oncology programs in a fast-paced, dynamic environment
  • Excellent verbal and written English communication skills
  • Have a high sense of responsibility and can respond quickly


Travel: Occasionally

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: $140,100.00 - $185,100.00 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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