Feasibility Associate

BeiGene

1d•$76,200 - $101,200

About The Position

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.

Requirements

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 preferably within the biotech, pharmaceutical sector, CRO, or clinical site environment.
Microsoft Office Suite, CTMS applications, EDC applications, analytic tools (e.g. Citeline, Trialtrove, etc.) and additional feasibility software

Nice To Haves

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

Responsibilities

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