Global Study Manager Jobs
Global Study Manager jobs are open across clinical research, pharmaceuticals, biotechnology, and academic research organizations, at every level from associate to senior and principal, with specializations in oncology trials, protocol development, and cross-functional site coordination. Find a role that fits below and apply directly.
Find Global Study Manager JobsOverview
Showing 5 of 14+ Global Study Manager jobs
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:
Accountable for global study delivery within agreed timelines and budget with appropriate inspection readiness quality- Leads all aspects of assigned clinical study(ies)
- Leads global cross-functional study team (including oversight of external partners) and acts as point of escalation for resolution of issues within assigned study(ies)
- Ensures alignment of study goals with clinical operations and corporate goals and objectives
- Experience in managing global oncology studies; preferably pivotal studies and inspection management with HA
Essential Functions of the job:
Cross-Functional Leadership
- Leads the global cross-functional study team effectively, ensures effective decision making, and acts as point of escalation for resolution of study related issues
- Leads external vendors management involved in study delivery
- Builds trust and relationship with regional subject matter experts and supports the delivery of their local study objectives
- Collaborates with key stakeholders across the organization and provides regular updates on study progress to senior management as required
- Represents the study team at internal meetings and leads the cross-functional Clinical Study Team (CST) meetings
- Participates and presents at various topics of Clinical Study Management
- Participates in Clinical Operations Process improvement initiative
Planning and Execution
- Leads planning and management of the assigned clinical study(ies) from feasibility through closeout activities
- Generates, manages, maintains, and communicates high quality study timelines and tracks progress towards these
- Ensures that the clinical studies are operationally feasible along with Global Clinical Program Lead, oversees trial feasibility, trial allocation and site selection process across all regions
- Ensures timely availability of high-quality study documents to allow study submission to regulatory authorities and ECs/IRBs
- Provides oversight to study start up and site activation plans
- Ensures study plans (eg project management plan, monitoring plan, Trial Master File plan, data monitoring plan, ...) are created, updated and distributed timely and implemented appropriately
- Ensures study systems and tools are set up timely, correctly and are functioning properly. Ensures study level information is updated on an ongoing basis in all systems
- Implements RBQM end-to-end processes on time within the allocated study (e.g., periodic reviews, centralized monitoring analyses, action items)
- Ensures relevant study specific training is developed and implemented and ensures training records are well documented and filed
- Ensures Trial Master File for study is created, maintained and QC’d on a regular basis as per the study TMF QC plan
- Collaborates closely with Global Clinical Supplies to forecast study drug and timely delivery of supplies to sites
- Supports and as needed drives overall data cleaning timelines in close collaboration with Data Management and other stakeholders (including but not limited to regional clinical operations teams and medicator monitor)
- Ensures planning and execution of the Clinical Study Report in collaboration with Medical Writing and relevant CST members
Quality and Risk Management
- Monitors study activities to ensure compliance with the study protocol, SOPs, all study plans, ICH/GCP and all other relevant regulations
- Regularly reviews and manages quality-related GCO metrics to be within acceptable limits
- Ensures inspection readiness at any point in time throughout the study life cycle
- Works with cross-functional study team to identify, interpret, and evaluate issues on the study and ensures corrective and preventative actions are implemented
- Ensures senior management and other key stakeholders are informed of risks and challenges and ensures risk mitigation plans are put in place and implemented
- Prepares team for quality assurance audits and inspections
- Collaborates with CST members and other colleagues to ensure cross-team, site learnings, and best practices are shared
- Leads improvements and partners with study team members to enhance the efficiency and the quality of the work performed on assigned studies
- Contributes to development, optimization and review of work instructions and SOPs as required
Budget and Resources
- Works with the sourcing team to select and manage study vendors, approving invoice payment throughout the study
- Manages study budgets, including baseline budget evaluation, change control, study closure budget, presents study budget for senior management engagement
- Adheres to clinical study budgeting processes and provides input to finance on budget accruals and forecasts
- Identifies and manages study team resource needs and establishes contingency plans for key resources.
- Monitors Clinical Study Team resource utilization over the study life cycle Ensures clinical studies at a project level are executed within endorsed time, quality, and cost parameters
Education Required:
Bachelor’s Degree in a scientific or healthcare discipline required*, Higher Degree preferred
- exceptions might be made for candidates with relevant clinical operations experience
Supervisory Responsibilities:
Provides performance feedback on team members as required
Computer Skills:
MS Office, Project Planning Applications, Clinical Trial Management Systems
Other Qualifications:
- Proven Project Management experience in Global Clinical Studies (Oncology experience preferred)
- Advanced knowledge of clinical operations methodologies, in depth understanding of all aspects of clinical study processes
- Able to independently lead global clinical studies (pivotal study management experience required)
- 5+ years of progressive experience in clinical research within biotech, pharma or CRO industry
Travel: Travel might be required as per business need.
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
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.
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:
Accountable for global study delivery within agreed timelines and budget with appropriate inspection readiness quality- Leads all aspects of assigned clinical study(ies)
- Leads global cross-functional study team (including oversight of external partners) and acts as point of escalation for resolution of issues within assigned study(ies)
- Ensures alignment of study goals with clinical operations and corporate goals and objectives
- Experience in managing global oncology studies; preferably pivotal studies and inspection management with HA
Essential Functions of the job:
Cross-Functional Leadership
- Leads the global cross-functional study team effectively, ensures effective decision making, and acts as point of escalation for resolution of study related issues
- Leads external vendors management involved in study delivery
- Builds trust and relationship with regional subject matter experts and supports the delivery of their local study objectives
- Collaborates with key stakeholders across the organization and provides regular updates on study progress to senior management as required
- Represents the study team at internal meetings and leads the cross-functional Clinical Study Team (CST) meetings
- Participates and presents at various topics of Clinical Study Management
- Participates in Clinical Operations Process improvement initiative
Planning and Execution
- Leads planning and management of the assigned clinical study(ies) from feasibility through closeout activities
- Generates, manages, maintains, and communicates high quality study timelines and tracks progress towards these
- Ensures that the clinical studies are operationally feasible along with Global Clinical Program Lead, oversees trial feasibility, trial allocation and site selection process across all regions
- Ensures timely availability of high-quality study documents to allow study submission to regulatory authorities and ECs/IRBs
- Provides oversight to study start up and site activation plans
- Ensures study plans (eg project management plan, monitoring plan, Trial Master File plan, data monitoring plan, ...) are created, updated and distributed timely and implemented appropriately
- Ensures study systems and tools are set up timely, correctly and are functioning properly. Ensures study level information is updated on an ongoing basis in all systems
- Implements RBQM end-to-end processes on time within the allocated study (e.g., periodic reviews, centralized monitoring analyses, action items)
- Ensures relevant study specific training is developed and implemented and ensures training records are well documented and filed
- Ensures Trial Master File for study is created, maintained and QC’d on a regular basis as per the study TMF QC plan
- Collaborates closely with Global Clinical Supplies to forecast study drug and timely delivery of supplies to sites
- Supports and as needed drives overall data cleaning timelines in close collaboration with Data Management and other stakeholders (including but not limited to regional clinical operations teams and medicator monitor)
- Ensures planning and execution of the Clinical Study Report in collaboration with Medical Writing and relevant CST members
Quality and Risk Management
- Monitors study activities to ensure compliance with the study protocol, SOPs, all study plans, ICH/GCP and all other relevant regulations
- Regularly reviews and manages quality-related GCO metrics to be within acceptable limits
- Ensures inspection readiness at any point in time throughout the study life cycle
- Works with cross-functional study team to identify, interpret, and evaluate issues on the study and ensures corrective and preventative actions are implemented
- Ensures senior management and other key stakeholders are informed of risks and challenges and ensures risk mitigation plans are put in place and implemented
- Prepares team for quality assurance audits and inspections
- Collaborates with CST members and other colleagues to ensure cross-team, site learnings, and best practices are shared
- Leads improvements and partners with study team members to enhance the efficiency and the quality of the work performed on assigned studies
- Contributes to development, optimization and review of work instructions and SOPs as required
Budget and Resources
- Works with the sourcing team to select and manage study vendors, approving invoice payment throughout the study
- Manages study budgets, including baseline budget evaluation, change control, study closure budget, presents study budget for senior management engagement
- Adheres to clinical study budgeting processes and provides input to finance on budget accruals and forecasts
- Identifies and manages study team resource needs and establishes contingency plans for key resources.
- Monitors Clinical Study Team resource utilization over the study life cycle Ensures clinical studies at a project level are executed within endorsed time, quality, and cost parameters
Education Required:
Bachelor’s Degree in a scientific or healthcare discipline required*, Higher Degree preferred
- exceptions might be made for candidates with relevant clinical operations experience
Supervisory Responsibilities:
Provides performance feedback on team members as required
Computer Skills:
MS Office, Project Planning Applications, Clinical Trial Management Systems
Other Qualifications:
- Proven Project Management experience in Global Clinical Studies (Oncology experience preferred)
- Advanced knowledge of clinical operations methodologies, in depth understanding of all aspects of clinical study processes
- Able to independently lead global clinical studies (pivotal study management experience required)
- 5+ years of progressive experience in clinical research within biotech, pharma or CRO industry
Travel: Travel might be required as per business need.
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
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.
Global Study Manager Jobs by Experience Level
See All 14 Global Study Manager Jobs
Find roles that match your experience and apply in just a few clicks.
Find Global Study Manager JobsGlobal Study Manager Job Market
Who's Hiring
What Employers Look For
The qualifications that appear most often in global study manager jobs.
- Bachelor's or advanced degree in life sciences, nursing, or a related clinical field
- Five or more years of clinical trial management experience across multiple phases
- Demonstrated knowledge of ICH-GCP guidelines and applicable regulatory requirements
- Experience managing CRO relationships, site contracts, and vendor oversight
- Proficiency with clinical trial management systems such as Veeva Vault or Medidata Rave
- Strong written communication skills for protocol development and regulatory submissions
Tips for Your Global Study Manager Job Search
Align your resume to ICH-GCP
Hiring managers for global study manager roles screen for explicit ICH-GCP compliance experience. Name specific phases, therapeutic areas, and regulatory submissions you've owned rather than listing general clinical research duties. Vague language gets filtered out fast.
Highlight cross-functional coordination wins
Global study manager roles require managing sites, CROs, vendors, and internal stakeholders at once. Your resume should show concrete examples of keeping multi-party timelines on track, not just your internal responsibilities. Outcomes matter more than job descriptions.
Apply early to roles that fit
Migrate Mate lists global study manager openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Target postings by therapeutic area
Oncology, rare disease, and CNS trials each have distinct protocol demands. Applying to roles within your therapeutic area signals depth rather than breadth. Filter your search by indication when possible and tailor your cover letter to that disease area's specific regulatory environment.
Prepare for scenario-based interview questions
Interviewers for global study manager positions routinely ask how you'd handle site underenrollment, protocol deviations, or CRO escalations mid-study. Practice walking through a real situation using a structured approach: the problem, your decision, and the outcome on timeline or data integrity.
Negotiate scope before you negotiate salary
Before accepting an offer, clarify the number of protocols you'll own simultaneously, the geographic footprint of your sites, and whether you'll manage direct reports. These variables determine workload and career trajectory far more than title or base pay alone.
Global Study Manager Jobs: Frequently Asked Questions
Which companies are hiring the most global study managers?
AbbVie, BeOne Medicines, and Regeneron are hiring the most global study managers right now, with openings concentrated in Illinois, California, and New Jersey, based on current listings on Migrate Mate as of November 2026. Pharmaceutical sponsors and large CROs consistently account for the highest volume of active postings.
How many global study manager jobs are remote?
About 88% of global study manager openings are fully remote or hybrid as of November 2026, with remote arrangements most common in protocol management, vendor oversight, and data review functions. Roles that require frequent site visits or hands-on investigator support are more likely to require a regional base or in-office presence.
How do you become a global study manager?
Start with a degree in a life science, nursing, or health-related field, then gain clinical operations experience as a clinical research associate or study coordinator handling site management and monitoring. Build up your phase II and III trial experience, develop familiarity with ICH-GCP and applicable regulations, and take on cross-functional project ownership before moving into a full study management role.
Can you get a global study manager job with limited experience?
Moving directly into a global study manager role with no clinical trial background is rare, but candidates who have worked as clinical research associates, site managers, or clinical project coordinators often transition successfully. Focus your applications on associate or junior study manager titles, emphasize any cross-functional coordination you've owned, and be specific about the therapeutic areas and phases you've supported.
What does the global study manager interview process look like?
Most employers run a phone or video screen with HR, followed by a competency-based interview with the hiring manager focused on protocol management, site escalation scenarios, and cross-functional coordination experience. A panel interview with clinical operations or medical affairs stakeholders typically follows, and some organizations include a case study or written exercise involving a mock protocol deviation or enrollment challenge.
Where can I find and apply to global study manager jobs?
You can find and apply to global study manager jobs on Migrate Mate, which lists current openings from across the United States. Find roles that match your therapeutic area, seniority, and location preferences, then apply directly to each listing from the page.
See All 14 Global Study Manager Jobs
Find roles that match your experience and apply in just a few clicks.
Find Global Study Manager Jobs