BeOne Medicines H-1B Visa Sponsorship Jobs USA
BeOne Medicines sponsors H-1B visas for roles in oncology drug development, clinical research, regulatory affairs, and bioinformatics. The company sponsors selectively, making it a viable target for specialized biotechnology and pharmaceutical professionals seeking U.S. work authorization in a research-driven environment.
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Get Access To All JobsINTRODUCTION
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.
ROLE AND RESPONSIBILITIES
- The Contract Manager is directly responsible for the supervision of administration and negotiation processes for clinical site contracts and ensures final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal & regulatory requirements. The Contracts Manager will identify clinical site contracts related issues and work together with other team members to propose and implement solutions.
Essential Functions of the Job:
- Oversight of planning, drafting, negotiating, tracking, and execution of site/investigator contracts which may be subcontracted to an external service provider or managed internally
- Ensures final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal and regulatory requirements
- Provide study-level oversight and guidance for clinical site contract negotiations, identify any potential risks, and be accountable for the overall contracting timelines/lifecycle in various regions
- Serve as the study-specific point of contact with the BeiGene Clinical Operations team and legal team on-site/investigator contract and budget matters
- Oversee a team of Site Contract Associates or equivalent at a Project level to ensure contracts in the region are completed per company standards/timelines. Implement mitigation plans as necessary in the assigned region
- Serve as an escalation point for unresponsive sites, site budget negotiations and ensure costs are approved within BeiGene FMV standards
- Adapts CBO’s plan and priorities to address resource and operational challenges
- Training and mentoring of new members of the local Contracts Team regarding financial/contractual issues and sharing experiences
- Contribute to process improvements, knowledge transfer and best practice sharing
- Ensure all agreements are executed in a timely manner, contributing to efficient site start-up timelines
- Organizes and prioritizes multiple initiatives and sets clear plans for delivery
- Effectively escalate/communicate to stakeholders and clinical teams in a professional and timely manner regarding contract issues that could impact project deliverables
- Responsible for management and administration of contracts and ensures compliance with corporate policies
- Serve as a backup to Site Contract Associates, as needed to handle out-of-office coverage
- Ensure proper delivery of fully executed clinical site contracts to CBO Payments teams and liaison with CBO payments team, as necessary
- Provide substantive guidance, monitoring, and support regarding clinical site contract deliverables, including undertaking activities identified in the CBO Roles/Responsibilities and/or Study Management Plan
- Review, apply, and maintain BeiGene Playbook to enhance the efficiency of negotiation in conjunction with BeiGene Legal
- Responsible for overseeing a Clinical Research Organization responsible for contract negotiations (if applicable)
- Responsible for clinical contract management, study metric tracking and reporting
- Active participant in various study meetings
- Prepare program/study status reports
- Maintains a system for tracking progress and status of clinical budget/contracts
- Support activities of various contracts and subsequent contract amendments note to files and other contract-related requests
- Assist colleagues with the resolution of problems related to site budget, contract terms and conditions, compliance with BeiGene policy, and any other site contract-related issues
- Deliver training to CBO colleagues or other Business Units as needed
- Serve as a point of escalation for sites that are unresponsive or slow to negotiate
- Create and develop effective contract templates and tools
- Performs other duties as assigned by management
- Works on Fair Market Value (FMV) analysis and processing of FMV exceptions (as needed)
- Provides cost benchmarking for clinical budget activities using industry-based system analysis (as needed)
SUPERVISORY RESPONSIBILITIES
- None
COMPUTER SKILLS
- Microsoft Office apps, CTMS, Contract Lifecycle Management System, Veeva, Jira, SharePoint etc.
OTHER QUALIFICATIONS
- Good knowledge of ICH-GCP, pharmaceutical related regulations and laws
- Good understanding of clinical trial contracting process, and relevant clinical operation practices
- Awareness and understanding of compliance and regulatory matters in clinical research
- Proven negotiation, interpersonal and business skills
- Strong planning and organizational skills and the ability to work independently and effectively in a dynamic environment with competing priorities
- Sense of urgency and strong goal orientation; track record of meeting deadlines and goals
- Strong written and verbal communication including written and verbal fluency in English and local language (if not English) and interpersonal skills, including conflict resolution and problem solving
- Proactive and positive team player. Able to maintain high performance during times of ambiguity and change in the work environment
- Experience in financial, budget, cost management/analysis, accounting, and/or financial planning skills are desirable
- Has knowledge of Intellectual Property issues, Publication issues, Indemnification issues and other standard issues of site contracts within the clinical research area
- Must be willing to work in a fast-paced environment with time-sensitive material
- Demonstrated ability to work effectively at all levels of an organization
TRAVEL
- Yes, 10%
EDUCATION / EXPERIENCE REQUIRED
- Bachelor's degree or equivalent work experience; Health Care, business, legal, or scientific discipline preferred
- Significant (at least 5 years) Clinical Research and/or contract/budget experience
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
COMPENSATION
- Salary Range: $118,600.00 - $158,600.00 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.
INTRODUCTION
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.
ROLE AND RESPONSIBILITIES
- The Contract Manager is directly responsible for the supervision of administration and negotiation processes for clinical site contracts and ensures final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal & regulatory requirements. The Contracts Manager will identify clinical site contracts related issues and work together with other team members to propose and implement solutions.
Essential Functions of the Job:
- Oversight of planning, drafting, negotiating, tracking, and execution of site/investigator contracts which may be subcontracted to an external service provider or managed internally
- Ensures final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal and regulatory requirements
- Provide study-level oversight and guidance for clinical site contract negotiations, identify any potential risks, and be accountable for the overall contracting timelines/lifecycle in various regions
- Serve as the study-specific point of contact with the BeiGene Clinical Operations team and legal team on-site/investigator contract and budget matters
- Oversee a team of Site Contract Associates or equivalent at a Project level to ensure contracts in the region are completed per company standards/timelines. Implement mitigation plans as necessary in the assigned region
- Serve as an escalation point for unresponsive sites, site budget negotiations and ensure costs are approved within BeiGene FMV standards
- Adapts CBO’s plan and priorities to address resource and operational challenges
- Training and mentoring of new members of the local Contracts Team regarding financial/contractual issues and sharing experiences
- Contribute to process improvements, knowledge transfer and best practice sharing
- Ensure all agreements are executed in a timely manner, contributing to efficient site start-up timelines
- Organizes and prioritizes multiple initiatives and sets clear plans for delivery
- Effectively escalate/communicate to stakeholders and clinical teams in a professional and timely manner regarding contract issues that could impact project deliverables
- Responsible for management and administration of contracts and ensures compliance with corporate policies
- Serve as a backup to Site Contract Associates, as needed to handle out-of-office coverage
- Ensure proper delivery of fully executed clinical site contracts to CBO Payments teams and liaison with CBO payments team, as necessary
- Provide substantive guidance, monitoring, and support regarding clinical site contract deliverables, including undertaking activities identified in the CBO Roles/Responsibilities and/or Study Management Plan
- Review, apply, and maintain BeiGene Playbook to enhance the efficiency of negotiation in conjunction with BeiGene Legal
- Responsible for overseeing a Clinical Research Organization responsible for contract negotiations (if applicable)
- Responsible for clinical contract management, study metric tracking and reporting
- Active participant in various study meetings
- Prepare program/study status reports
- Maintains a system for tracking progress and status of clinical budget/contracts
- Support activities of various contracts and subsequent contract amendments note to files and other contract-related requests
- Assist colleagues with the resolution of problems related to site budget, contract terms and conditions, compliance with BeiGene policy, and any other site contract-related issues
- Deliver training to CBO colleagues or other Business Units as needed
- Serve as a point of escalation for sites that are unresponsive or slow to negotiate
- Create and develop effective contract templates and tools
- Performs other duties as assigned by management
- Works on Fair Market Value (FMV) analysis and processing of FMV exceptions (as needed)
- Provides cost benchmarking for clinical budget activities using industry-based system analysis (as needed)
SUPERVISORY RESPONSIBILITIES
- None
COMPUTER SKILLS
- Microsoft Office apps, CTMS, Contract Lifecycle Management System, Veeva, Jira, SharePoint etc.
OTHER QUALIFICATIONS
- Good knowledge of ICH-GCP, pharmaceutical related regulations and laws
- Good understanding of clinical trial contracting process, and relevant clinical operation practices
- Awareness and understanding of compliance and regulatory matters in clinical research
- Proven negotiation, interpersonal and business skills
- Strong planning and organizational skills and the ability to work independently and effectively in a dynamic environment with competing priorities
- Sense of urgency and strong goal orientation; track record of meeting deadlines and goals
- Strong written and verbal communication including written and verbal fluency in English and local language (if not English) and interpersonal skills, including conflict resolution and problem solving
- Proactive and positive team player. Able to maintain high performance during times of ambiguity and change in the work environment
- Experience in financial, budget, cost management/analysis, accounting, and/or financial planning skills are desirable
- Has knowledge of Intellectual Property issues, Publication issues, Indemnification issues and other standard issues of site contracts within the clinical research area
- Must be willing to work in a fast-paced environment with time-sensitive material
- Demonstrated ability to work effectively at all levels of an organization
TRAVEL
- Yes, 10%
EDUCATION / EXPERIENCE REQUIRED
- Bachelor's degree or equivalent work experience; Health Care, business, legal, or scientific discipline preferred
- Significant (at least 5 years) Clinical Research and/or contract/budget experience
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
COMPENSATION
- Salary Range: $118,600.00 - $158,600.00 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.
Job Roles at BeOne Medicines
How to Get Visa Sponsorship in BeOne Medicines H-1B Visa Sponsorship Jobs USA
Target roles aligned with BeOne's oncology pipeline
BeOne Medicines focuses on cancer therapeutics, so H-1B sponsorship tends to flow toward clinical development, translational medicine, and regulatory science roles. Applying to positions directly tied to their drug pipeline improves your chances of sponsorship consideration.
Verify active sponsorship before applying
Not every biotech company sponsors consistently across all departments. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, helping you confirm BeOne Medicines is actively filing H-1B petitions before investing time in an application.
Highlight specialized scientific credentials early
BeOne's H-1B filings tend to reflect highly specialized roles requiring advanced degrees in life sciences, chemistry, or biostatistics. Lead your resume and cover letter with your specific degree field and relevant research experience to signal immediate eligibility.
Understand the H-1B lottery timing relative to hiring cycles
The H-1B cap lottery runs in March for an October 1 start date. When interviewing at BeOne Medicines, clarify whether your role qualifies for cap-exempt processing or requires lottery selection, as this affects your earliest possible start date significantly.
Engage BeOne's talent acquisition team directly
Biotechnology and pharmaceutical companies often route H-1B sponsorship decisions through both HR and legal teams. Asking directly about sponsorship willingness during recruiter screens signals immigration awareness and avoids wasted time on roles not approved for visa support.
Demonstrate long-term value in a research-intensive setting
BeOne Medicines invests in multi-year clinical programs, so emphasizing your potential for sustained contribution to ongoing research or regulatory submissions strengthens the business case your employer needs to justify initiating an H-1B petition on your behalf.
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Get Access To All JobsFrequently Asked Questions
Does BeOne Medicines sponsor H-1B visas?
Yes, BeOne Medicines sponsors H-1B visas for qualifying roles. Sponsorship at BeOne is concentrated in specialized scientific and clinical functions within its oncology and biotechnology operations. As with most pharmaceutical companies, not every open position is approved for sponsorship, so confirming with the recruiter early in the process is advisable.
Which roles and departments at BeOne Medicines typically receive H-1B sponsorship?
H-1B sponsorship at BeOne Medicines tends to concentrate in roles requiring advanced scientific expertise, including clinical development, regulatory affairs, bioinformatics, pharmacokinetics, and translational research. Positions requiring a specific degree in a defined field, such as a Ph.D. in oncology biology or a master's in biostatistics, are well-suited to the specialty occupation standard the H-1B requires.
How do I navigate the H-1B application process at BeOne Medicines?
After receiving a job offer, BeOne Medicines works with an immigration attorney to file a Labor Condition Application with the Department of Labor and then submit Form I-129 to USCIS. If your role is cap-subject, your petition enters the annual lottery. Cap-exempt positions, such as those based at qualifying research institutions, bypass the lottery entirely. Your HR contact will coordinate timelines with legal counsel.
How long does H-1B sponsorship take at BeOne Medicines?
For cap-subject petitions, the process starts with lottery registration in March and, if selected, the visa becomes effective October 1. Total time from offer to work authorization can exceed six months. Premium processing, which expedites USCIS adjudication to roughly 15 business days for an additional fee paid by the employer, is available and commonly used in pharmaceutical hiring to reduce uncertainty.
How do I find open H-1B jobs at BeOne Medicines?
Start by searching BeOne Medicines directly on their careers page, then cross-reference with a platform that tracks verified sponsorship activity. Migrate Mate lets you filter biotechnology employers by actual H-1B filing history, so you can confirm sponsorship willingness before applying rather than discovering late in the process that a role is not approved for visa support.
What is the prevailing wage for H-1B jobs at BeOne Medicines?
H-1B employers must pay at least the prevailing wage, which is determined when they file the Labor Condition Application with the Department of Labor. The rate is based on the role, location, and experience level, and ensures international hires are paid comparably to U.S. workers in the same position. You can look up prevailing wage rates for any occupation and location using the DOL's OFLC Wage Search tool.
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