Serve as a flexible Study Manager for IITs across NAMA, JAPAC, EU and New Market regions * Oversee operational execution of the entire lifecycle IIT studies, including feasibility, operational review ...

60 Beigene Operations Manager Jobs Hiring Near You
Serve as a flexible Study Manager for IITs across NAMA, JAPAC, EU and New Market regions * Oversee operational execution of the entire lifecycle IIT studies, including feasibility, operational review ...
In this role, the Director will work toward standardization of key operational activities across Global Medical Affairs (GMA) and provide Project Management support for the GMA Leadership Team. The ...
In this role, the Director will work toward standardization of key operational activities across Global Medical Affairs (GMA) and provide Project Management support for the GMA Leadership Team. The ...
Senior Director, Program & Portfolio Governance
$190K - $260K/yr
This role ensures alignment between strategic objectives, business priorities, and operational execution effective program management, and portfolio governance across the organization. The position ...
Senior Director, Program & Portfolio Governance
$190K - $260K/yr
This role ensures alignment between strategic objectives, business priorities, and operational execution effective program management, and portfolio governance across the organization. The position ...
Leveraging deep Therapeutic Area expertise, solid global program management skills, global view, and borderless leadership, the GCO Program Lead is accountable for the strategic operational planning ...
Leveraging deep Therapeutic Area expertise, solid global program management skills, global view, and borderless leadership, the GCO Program Lead is accountable for the strategic operational planning ...
Acts as the CSM statistician interfacing with clinical study statisticians, medical monitors, safety/pharmacovigilance, global clinical operations (GCO), quality/GCP, data management to ensure ...
Acts as the CSM statistician interfacing with clinical study statisticians, medical monitors, safety/pharmacovigilance, global clinical operations (GCO), quality/GCP, data management to ensure ...
Director, Global Regulatory Project Management
$153K - $202K/yr
... operational execution, and ensuring all cross-functional activities are coordinated and delivered ... This role has the potential to evolve into a formal people-manager position. Over time, ...
Director, Global Regulatory Project Management
$153K - $202K/yr
... operational execution, and ensuring all cross-functional activities are coordinated and delivered ... This role has the potential to evolve into a formal people-manager position. Over time, ...
Director, Clinical Supply Chain
$166K - $226K/yr
Builds strong relationships with BeOne's functional management (including but not limited to Clinical Operations, Regulatory Affairs, CMC, Quality, and Clinical Development) to ensure alignment of ...
Director, Clinical Supply Chain
$166K - $226K/yr
Builds strong relationships with BeOne's functional management (including but not limited to Clinical Operations, Regulatory Affairs, CMC, Quality, and Clinical Development) to ensure alignment of ...
Senior Engineer I, Validation
Pennington, NJ · On-site
Leading and Managing projects for the validation of equipment, processes, and products to meet all safety, quality, regulatory and operational requirements * Review of equipment specification/design ...
Senior Engineer I, Validation
Pennington, NJ · On-site
Leading and Managing projects for the validation of equipment, processes, and products to meet all safety, quality, regulatory and operational requirements * Review of equipment specification/design ...
Partner with manufacturing, quality assurance, quality control, regulatory affairs, clinical operations, development, patient safety and other stakeholders to ensure timely and thorough management of ...
Partner with manufacturing, quality assurance, quality control, regulatory affairs, clinical operations, development, patient safety and other stakeholders to ensure timely and thorough management of ...
Senior Workplaces Services & Projects Coordinator
Pennington, NJ · On-site
$39.47 - $53.47/hr
Facilities Operations: * Oversee the maintenance, cleanliness, and safety of the office or facility ... Manage room bookings, catering, audiovisual equipment, and any other necessary arrangements.
Senior Workplaces Services & Projects Coordinator
Pennington, NJ · On-site
$39.47 - $53.47/hr
Facilities Operations: * Oversee the maintenance, cleanliness, and safety of the office or facility ... Manage room bookings, catering, audiovisual equipment, and any other necessary arrangements.
Leveraging deep Therapeutic Area expertise, solid global program management skills, global view, and borderless leadership, the GCO Program Lead is accountable for the strategic operational planning ...
Leveraging deep Therapeutic Area expertise, solid global program management skills, global view, and borderless leadership, the GCO Program Lead is accountable for the strategic operational planning ...
Senior Analyst, QC Chemistry, Capillary Electrophoresis (Hopewell, NJ)
Hopewell, NJ · On-site
$90K - $125K/yr
Support routine operations, including but not limited to instrument qualification and maintenance ... Manage inventory of reagents and supplies for the laboratory. * Participate in internal and ...
Senior Analyst, QC Chemistry, Capillary Electrophoresis (Hopewell, NJ)
Hopewell, NJ · On-site
$90K - $125K/yr
Support routine operations, including but not limited to instrument qualification and maintenance ... Manage inventory of reagents and supplies for the laboratory. * Participate in internal and ...
Medical Director, Hematology
$249K - $309K/yr
Specifically, the incumbent will work closely with colleagues in clinical development, program management, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics ...
Medical Director, Hematology
$249K - $309K/yr
Specifically, the incumbent will work closely with colleagues in clinical development, program management, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics ...
Leveraging deep Therapeutic Area/Asset expertise, solid global program management skills, global view, and borderless leadership, the GCO Franchise Head is accountable for the strategic operational ...
Leveraging deep Therapeutic Area/Asset expertise, solid global program management skills, global view, and borderless leadership, the GCO Franchise Head is accountable for the strategic operational ...
Director, Drug Product Manufacturing (Hopewell, NJ)
Hopewell, NJ · On-site
$167K - $227K/yr
This position reports directly to the General Manager (Site Head) and is a site leadership position ... Responsibilities also include CQV commissioning, GMP readiness, commercial operation and delivery ...
Director, Drug Product Manufacturing (Hopewell, NJ)
Hopewell, NJ · On-site
$167K - $227K/yr
This position reports directly to the General Manager (Site Head) and is a site leadership position ... Responsibilities also include CQV commissioning, GMP readiness, commercial operation and delivery ...
Actively promote and reinforce a culture of integrity, ensuring compliance is embedded into daily business operations and decision-making. * Manage compliance communication resources, including the ...
Actively promote and reinforce a culture of integrity, ensuring compliance is embedded into daily business operations and decision-making. * Manage compliance communication resources, including the ...
Responsible for the business operations of the Program and Study Management (P&SM) function, driving operational excellence, innovation, and continuous process improvement from strategic planning ...
Responsible for the business operations of the Program and Study Management (P&SM) function, driving operational excellence, innovation, and continuous process improvement from strategic planning ...
Associate Director, Drug Substance Manufacturing (Hopewell, NJ)
Hopewell, NJ · On-site
$139K - $189K/yr
This position reports directly to the General Manager (Site Head) and is a site leadership position ... Responsibilities also include CQV commissioning, GMP readiness, commercial operation and delivery ...
Associate Director, Drug Substance Manufacturing (Hopewell, NJ)
Hopewell, NJ · On-site
$139K - $189K/yr
This position reports directly to the General Manager (Site Head) and is a site leadership position ... Responsibilities also include CQV commissioning, GMP readiness, commercial operation and delivery ...
Develop and implement integrated account strategies synchronized with NAMA, R&D, Market Access, Clinical Operations, and Franchise/Commercial Leadership objectives * Support change management efforts ...
Develop and implement integrated account strategies synchronized with NAMA, R&D, Market Access, Clinical Operations, and Franchise/Commercial Leadership objectives * Support change management efforts ...
Associate Director, Regional Marketing
$155K - $205K/yr
Partner with Sales, Medical Affairs, Market Access, and Commercial Operations & Business Analytics ... ability to manage and refine workflow processes with Excel. Travel: * 50% or more Global ...
Associate Director, Regional Marketing
$155K - $205K/yr
Partner with Sales, Medical Affairs, Market Access, and Commercial Operations & Business Analytics ... ability to manage and refine workflow processes with Excel. Travel: * 50% or more Global ...
BeiGene Jobs Information

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 27 days ago
Job description
General Description:
The Associate Director, IIT Operations will play a supportive leadership role within the BeOne IIT Team, providing strategic and operational oversight across the global Investigator-Initiated Trials (IIT) program. This role is responsible for centralized project management of all IIT projects and initiatives, serving as a floating Study Manager across regions as needed, and leading research-focused collaborations with external investigators and academic partners.
This individual will work cross-functionally with Medical Affairs, Clinical Development, Regulatory, Legal, Compliance, Contracts, and other key partners to ensure high-quality, compliant, and timely execution of the IIT portfolio. The Associate Director will also support process optimization, KPI tracking, and program-level governance efforts.
Essential Functions of the Job:
IIT Study Management (~60%)
- Serve as a flexible Study Manager for IITs across NAMA, JAPAC, EU and New Market regions
- Oversee operational execution of the entire lifecycle IIT studies, including feasibility, operational review, contracting, study start-up, drug supply coordination, monitoring progress, and study closeout.
- Responsible for ensuring the grant management system is always up-to-date with current information from the sponsor-investigator and assess impact on changes in assumption (e.g., changes to enrollment projections, timeline and downstream effects on payment milestones).
- Close collaboration with regional IIT leads, field team, medical leads and leadership to address underperforming studies and strategize on a risk mitigation plan. Study managers are expected to assess for early warning signs of enrollment and timeline deviation and escalate ASAP.
- Close collaboration with IIT budget forecast tracker lead and Finance in managing study budgets and milestone payments.
- Ensure all activities are conducted in compliance with BeOne policies, SOPs, GCP, and regional regulations.
- Act as the primary operational contact for investigators, research sites, partners, and internal stakeholders.
- Oversee IIT agreement negotiations to ensure efficient processing and escalation of potential issues.
IIT Research Collaborations (~20%)
- Project management of solicited and unsolicited research partnerships and scientific collaborations with academic institutions, cooperative groups, and key research networks.
- Support development of collaboration frameworks, data-sharing agreements, and joint project plans.
- Facilitate scientific and operational discussions to advance external research aligned with the Medical/Scientific strategy.
- Ensure collaboration milestones, deliverables, and expectations are met.
Project Management of IIT Initiatives (~15%)
- Lead end-to-end project management of all IIT team initiatives, including process improvements, system enhancements, governance updates, and portfolio-level activities.
- Develop project plans, timelines, risk logs, communication plans, and resource assessments for all IIT projects.
- Drive cross-functional collaboration and ensure alignment with internal stakeholders across Medical Affairs, Clinical Development, Legal, Compliance, and Finance.
- Monitor progress and proactively address risks, bottlenecks, and dependencies that may impact team goals.
- Support development and presentation of project dashboards, metrics, and reports for senior leadership and governance committees.
- Contribute to development and refinement of IIT processes, SOPs, work instructions and checklist documents.
- Support implementation and optimization of IIT systems/platforms (e.g., submission portals, tracking systems).
- Identify opportunities to drive operational excellence, standardization, and efficiency across the IIT program.
MIRC Governance Support & Back-up Coverage (~5%)
- Support Medical Internal Review Committee (MIRC) Lead in operational review of proposals and protocols. Responsibilities include scheduling, agenda and slide preparation, adjudicating comments, creating meeting minutes and following up on action items.
- To ensure business continuity, this role will perform as the primary back-up to the MIRC for short-term coverage.
Required Education:
- BA/BS Degree is required, Advanced degree (MD/PharmD, MS) is preferred.
Required Qualifications:
- MD/PharmD with 4 + years of experience within the pharmaceutical industry, clinical research, consulting and/or CRO.
- Masters Degree with 6 + years of experience within the pharmaceutical industry, clinical research, consulting and/or CRO.
- Bachelors Degree with 8 + years of experience within the pharmaceutical industry, clinical research, a consulting and/or CRO.
- 5+ years of experience in clinical research, project management, Medical Affairs operations, or IIT management(Preferred).
- Prior operational experience managing preclinical and clinical IITs (IST, ISR, external research collaborations).
- Demonstrated experience managing clinical research projects or programs in a pharma, biotech, or academic research setting.
- Strong understanding of GCP, clinical research regulations, and IIT operational workflows.
- Excellent project management, prioritization, organizational skills, decision-making, and time management skills in a fast-paced environment.
- Exceptional communication and interpersonal skills with the ability to influence without authority.
- Proven ability to work independently in a fast-paced, matrixed environment.
- Prior experience in IIT governance committee, PMP/or equivalent, people management, a plus.
Supervisory Responsibilities:
- No direct reports
- Role may provide mentorship to junior colleagues
- Role may provide short-term leadership coverage to the IIT lead to ensure business continuity
Computer Skills:
- Microsoft Office Suite
- Power BI dashboard
- Smartsheet
- Grants management submission portal software
- Clinical Trial Management Software (CTMS) or other study management software
- Familiarity with other industry applications such as: Veeva, Agiloft and SAP Ariba
Role Specific Competencies
- Strategic thinking and problem-solving
- Cross-functional leadership
- Relationship and stakeholder management
- Operational excellence and execution focus
- Adaptability and resourcefulness
- Scientific/clinical literacy
- Strong ethical judgment and compliance-mindset
Travel:
- Work related travel approximately 5-10%.
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: $160,100.00 - $210,100.00 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.
About BeiGene
Sourced by ZipRecruiter
BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .
Industry
Health care and social assistance
Company size
5,001 - 10,000 Employees
Headquarters location
Cambridge, MA, US
Year founded
2010