(Senior) Associate, Clinical Site Budget Planning

BeOne Medicines; Kuala Lumpur; On-site; MYR 134,000 - 201,000; Full time

Benefits offered by this job

Market competitive compensation

Learning and development opportunities

BeOne shares

Job summary

BeOne Medicines seeks an experienced (Senior) Associate to develop accurate site budgets for BeOne-sponsored clinical trials and guide FMV negotiations with clinical sites. This role requires collaboration with Clinical Operations and other stakeholders to ensure budgets meet protocol requirements.

The ideal candidate has a Bachelor’s degree with 3+ years in finance or clinical research, strong English communication, and proficiency in budget tools.

Qualifications

• Bachelor’s degree and 3+ years’ experience in finance, business, clinical research or related field.
• Fluent in English with excellent communication and writing skills.
• Solid understanding of FMV benchmarking tools and CPT codes.

Responsibilities

• Develop trial-level and country-level site budgets in line with industry standards and local requirements.
• Collaborate with Clinical Operations and relevant stakeholders to build site budgets compliant with study protocols.
• Provide site budget deliverables for governance committees and FMV negotiations with clinical sites.
• Participate in budget development life cycle from inception to close-out and perform variance analysis.
• Mentor, train and support junior associates in budget development processes.
• Contribute to process improvements and training for new budget templates and tools.

Skills

Fluent English

Analytical skills

Problem solving

Detail oriented

Independent worker

Teamwork

Education

Bachelor’s degree in finance, business, clinical research or related field

Tools

Microsoft Word

Microsoft Excel

PowerPoint

MS Outlook

Smartsheet

SharePoint

MS Teams

Job description

About Us

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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:

The (Senior) Associate is responsible for the development of accurate and compliant investigator grants(“site budgets”) that facilitate trial-level financial planning and forecasting activities and guide fair market value (FMV) negotiations with clinical sites for BeOne-sponsored clinical trials.

Works under limited supervision and guidance. Serves as a subject matter expert in the site budget development, able to identify and resolve issues that arise. Able to lead complex site budget development and analysis.

Essential Functions Of The Job

• Responsible for the development of trial-level and country-level site budgets that are in line with industry standards and local requirements, leveraging FMV benchmarking tools, BeOne Rate Cards, established systems, databases and processes.
• Work effectively with Clinical Operations (i.e. Clinical Study Managers (CSM), Clinical Project Lead (CPL), Clinical Site Contract Managers (CM), etc.) and relevant stakeholders (i.e. Medical Directors, Global Research & Development Sourcing (GRDS), R&D Finance, etc.) to build site budgets in compliance with the study protocol requirements, study assumptions, applicable policies, procedures, and objectives.
• Provide site budget deliverables: a) for submission to BeOne governance committees (e.g. Development Review Committee (DRC), Clinical Finance Review Committee (CFRC)) for the purpose of financial planning, forecasting, and data-driven strategic decisions for the study/trial; and/or b) to Clinical Operations (CSM and CM) to support efficient and compliant FMV negotiations with clinical sites for the study/trial.
• Serve as a member of the BeOne Estimate Support Team (BEST), providing site budget estimates throughout the protocol life cycle (from inception to close-out of the clinical trial) for financial planning and forecasting. Perform budget variance analysis, scenario modeling, and benchmark assessments to support strategic decision-making of the business.
• Work on assigned site budget requests from internal stakeholders for a study/trial.
• Analyze protocol amendments and/or changes to trial/study assumptions, to determine impact to site budgets, identify costs drivers of budget variances from prior site budget version
• Lead complex site budget development and analysis.
• Provide strategic insight, when required, into budget development process with difficult protocol situations (complex protocols, difficult therapeutic areas with high priority studies)
• Organize meetings with stakeholders to resolve queries, obtain required information and approvals in order to drive the timely development of accurate site budgets.
• Actively tracks and effectively communicates status of site budget development with CBO leadership and key internal stakeholders in a timely manner.
• Coordinates with internal stakeholders to ensure study start-up (SSU) activities are aligned with site budget activities and mutually agreed upon timelines for site activation. Effectively communicates issues to stakeholders that could impact project timelines or other aspects of SSU.
• Contribute to process improvement initiatives, including but not limited to, development and training for new site budget templates, updates to guidance, processes, checklists, trackers, tools, knowledge sharing, etc.
• Conduct peer quality control (QC) checks of site budgets.
• Mentor, train and support junior associates in budget development processes
• Develop, maintain, and train stakeholders on budget development documents and processes.
• Undertake other duties as requested by departmental and company leadership.

Qualification Required

Education Required:

Bachelor’s degree from an accredited college or university, and 3+ years’ experience in finance, business, clinical research or related field in the biotech or pharmaceuticals industry.

Other Qualifications

• Fluent in English with excellent communication and writing skills.
• Strong interpersonal, analytical, numerical and problem‑solving skills.
• Good organizational skills with the ability to manage multiple deliverables and competing priorities.
• Detail and process oriented.
• Capable of working independently or in a team environment.
• Solid understanding of FMV benchmarking tools and CPT codes.
• Proficiency in site budget development, analysis and modelling techniques.
• Prior experience in clinical operations, finance, site contract or site payment positions.
• Understanding of ICH GCP guidelines and clinical research processes.

Supervisory Responsibilities

• No

Computer Skills

• Advanced knowledge Microsoft Office software - Word, Excel, Power Point and MS Outlook; Smartsheet, SharePoint, MS Teams

Travel

• As needed

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

• 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.