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Feasibility Associate

Role overview

Qualifications

  • Bachelor’s degree or higher in a scientific or healthcare discipline preferred
  • Minimum of 2 years of progressive experience in clinical research and clinical operations
  • Experience preferably within the biotech, pharmaceutical sector, CRO, or clinical site environment

Responsibilities

  • Maintain detailed records of work and create and maintain internal libraries and databases
  • Support cross-functional meetings and prepare relevant meeting materials
  • Resolve feasibility issues during site selection of clinical trials
  • Participate in activities associated with Country Feasibility and/or Site Feasibility for regional and country clinical trials

Key facts

  • Remote from: United States
  • Full time
  • Mid-level (2-5 years)
  • English

Hard skills

Other skills

  • Microsoft Office
  • Teamwork
  • Self-Awareness
  • Entrepreneurship
  • Results Focused
  • Analytical Thinking
  • Communication

About the company

BeiGene logo

BeiGene

Biotechnology

BeiGene is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer 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 10,000 colleagues spans five continents. To learn more about BeiGene, please visit www.beigene.com and follow us on LinkedIn, X (formerly known as Twitter) and Facebook.

Company details

Company typeXLarge
IndustryBiotechnology
Company size10001

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Job description

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:

Maintains detailed records of work and creates and maintains internal libraries and databases, while also remaining informed of current scientific and clinical research being conducted.

  • Support cross-functional meetings and prepare relevant meeting materials.
  • Resolve the feasibility issues during site selection of clinical trials.
  • Optimize and improve the quality of feasibility related data resources and materials.

Essential Functions of the job:

  • Participate in activities associated with Country Feasibility and/or Site Feasibility for regional and country clinical trials for the larger or more complex trial opportunities.
  • Support clinical trial efforts through data mining of internal databases, review of investigators for quality assurance and development of prioritize site list based on historic site performance and capability
  • Reconcile and interpret feasibility data. Extrapolate data collected to provide a country-level assessment.
  • May liaise with internal and external customers to coordinate the collection and delivery of feasibility data.
  • Review site lists for accuracy and update information as required.
  • Conduct CDA outreach and execute required documents for feasibility activities.
  • Serve as the primary feasibility contact for assigned studies.
  • Manage feasibility outreach activities and coordinate investigator engagement efforts to assess study interest and site capabilities
  • Collaborate closely with Clinical Operations, Site Management, Data Sciences, Medical Affairs, and external partners to ensure feasibility deliverables are completed on time and to quality expectation
  • Participate in study kickoff meetings, feasibility strategy discussions, and enrollment planning meetings
  • Support process improvement initiatives and contribute to the enhancement of feasibility methodologies, templates, and data resources.
  • Support onboarding and training activities within the feasibility organization.
  • Contribute to development of standardized processes, training materials, and operational efficiencies

Computer Skills:

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

Travel:

  • Travel might be required as per business need

Education / Experience:

  • Bachelor’s degree or higher in a scientific or healthcare discipline preferred with minimum of 2 years of progressive experience in clinical research and clinical operations preferably within the biotech, pharmaceutical sector, CRO, or clinical site environment.

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: $76,200.00 - $101,200.00 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 accommodationsus@beonemed.com.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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