About us
BeOne 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, with administrative offices in Basel, Beijing, and Cambridge, U.S. To learn more about BeOne, please visit www.beonemedicines.com and follow us on LinkedIn and X (formerly known as Twitter).
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.
Job Description:
General Description:
Supports the Global Clinical Study Manager in global study delivery and ensures that delegated components of clinical studies are executed to expected and specified quality standards, within timelines and budget
Supports the alignment of study goals with clinical operations goals and objectives under direction of the Global Clinical Study Manager
Supports study vendor management in addition to other study management activities assigned
Essential Functions of the Job:
Cross-Functional Leadership Support & Collaboration
Supports the Global Clinical Study Manager with the organization and logistics for cross-functional Clinical Study Team (CST) meetings
Establishes good collaboration with the Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally
Knowledgeable of clinical study operations, including interpretation and implementation of regulatory and ICH-GCP guidelines
Builds solid knowledge of global clinical trials operations under the guidance of the Global Clinical Study Manager
Actively contributes to GSMA task force initiatives and cross functional projects within scope, supporting process improvement, standardization, and implementation activities as required
•Planning and Execution
Creates and maintains study-level SharePoint and CST distribution lists
Sets up the study in the appropriate systems e.g. eTMF, CTMS etc and makes sure study-level information is kept up to date
Ensures system access is granted and managed appropriately across the study life cycle, supports user account management for systems used in study
Supports the development of various study plans
May assist in the review of study-related documents as delegated by the Global Clinical Study Manager (e.g., Clinical protocols, Informed consent forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Pharmacy Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters)
Organizes study-specific investigator meetings under supervision of the Global Clinical Study Manager
Might support the creation and review of site feasibility assessments required for study participation
Manages and tracks key study deliverables such as screening, enrollment, biological samples and images, data flow and protocol deviations in relevant systems in collaboration with Regional Clinical Trial Management Associates
Prepares metrics and updates to key deliverables for management as per information available in relevant systems
Supports the preparation of a study newsletter and other correspondence related to the study conduct (e.g. frequently asked questions, lessons learned) in collaboration with the study team
Supports the TMF specialist with study-level TMF creation and, as required, maintains the study-level TMF, including regular review and QC of TMF documents as per the study TMF QC plan
Supports the Global Clinical Study Manager with study drug forecasts and overall study drug supply activities in collaboration with Global Clinical Supplies
Supports the overall data cleaning activities and contributes to the follow-up of outstanding information
Supports the Global Clinical Study Manager with planning and execution of the Clinical Study Report
Quality
Supports the identification of operational risks and issues and works with the Global Clinical Study Manager to recommend solutions for discussion with appropriate team leadership
Learns and shares best practices in clinical operations methodologies, systems and processes with an emphasis on quality and compliance
Suggest improvements to enhance efficiency and the quality of the work performed on assigned projects
Might support the development of global study tools, working instructions and SOPs
Budget
Supports selection and set-up of vendors for global outsourced activities
Supports study budget management activities with responsibility for PO setup and payment invoice tracking across all study lifecycles.
Supervisory Responsibilities:
Might mentor junior team members/onboarding of new hires
Qualification Required:
Education Required: Bachelor or higher degree in a scientific or healthcare discipline*, higher degree preferred.
Computer Skills:
Proficiency in MS Office Suite, including Excel, PowerPoint, and Project etc.
Other Qualifications:
Knowledge of clinical operations methodologies, understanding of operational aspects of clinical study processes
3 or more years of experience in clinical research within Biotech, Pharma or CRO industry
Travel:
Limited travel might be required
What We Offer To Our Valued Employees
Market competitive compensation package including performance-based annual bonus scheme
Company shares (generous welcome grant!)
In-house and external learning and development opportunities
Fantastic benefits program and keep improving!
Plus you get to work with a dynamic team of collaborative, supportive, inclusive, and fun professionals whose mission is clear: Cancer has no borders and neither do we.
Join us and Make momentum in your career!
BeOne Global Competencies
When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, 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
BeOne is committed to respect and protect personal information rights of job applicants and will process job applicants’ personal information in accordance with applicable laws and regulations.
Due to BeOne’s global operation, job applicants’ data will be stored overseas with adequate protection. Besides, job applicants’ data will be stored for no longer than is necessary to facilitate potential application for other suitable positions in BeOne. For further details, please refer to BeOne’s Job Applicant Privacy Policy (https://beonemedicines.com/privacy-policy).
If you voluntarily provide your personal information to us, it is deemed as you have acknowledged and consented to (if required by the applicable laws) BeOne’s Job Applicant Privacy Policy as well as the relevant privacy terms. If you voluntarily provide the personal information of other job applicants to us, it is deemed as you have ensured that the relevant individuals have acknowledged and consented to (if required by the applicable laws) BeOne’s Job Applicant Privacy Policy as well as the relevant privacy terms.
If you have any concern, please DO NOT provide any resume or other personal information to us.
Skills Required
- Bachelor degree in a scientific or healthcare discipline
- Higher degree (preferred)
- Three or more years experience in clinical research within Biotech, Pharma, or CRO
- Proficiency in MS Office (Excel, PowerPoint, Project)
- Experience with SharePoint, eTMF, CTMS and TMF maintenance/QC
- Knowledge of clinical operations methodologies and interpretation/implementation of regulatory and ICH‑GCP guidelines
- Experience supporting vendor management, study budget activities, PO setup and invoice tracking
- Ability to support preparation of study deliverable metrics, investigator meetings, and study correspondence
BeiGene Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about BeiGene and has not been reviewed or approved by BeiGene.
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Equity Value & Accessibility — Equity grants and stock programs are widely available across roles, including RSU grants at hire and opportunities to participate in company equity plans. Total compensation commonly includes equity alongside base pay and incentives.
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Healthcare Strength — Health coverage is described as comprehensive and high quality, with multiple mentions of “top notch” medical benefits. This strength is consistently highlighted as a key component of the package.
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Retirement Support — Retirement offerings include a 401(k) with a competitive employer match. These features contribute to a strong overall compensation bundle.
BeiGene Insights
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
