Senior Program Manager, Global Clinical Training and Programming Job at Spring Health

New

Senior Program Manager, Global Clinical Training and Programming

Reporting to the Director of Clinical Training, the Senior Program Manager, Clin...

Location

Japan , Tokyo

Salary:

8964800.00 - 10309520.00 JPY / Year

Spring Health

Expiration Date

Until further notice

Requirements

Clinical license or equivalent in your country
3-5 years of experience in facilitation and event planning
Complete knowledge and understanding of the unique global challenges, potential solutions, and Clinical Training and Programming
Complete knowledge of Program Management and data evaluation
Complete knowledge of Google Suite, Zoom, and additional events platforms as needed
Solid understanding of instructional design and content development, including strong working knowledge of Adult Learning Principals
Knowledgeable about training evaluation techniques
Communicate effectively with customers and fellow Spring team members

Job Responsibility

Serve as the primary Project Manager for Global (Non US) Clinical Training and Programming
Serve as a SME on Global Clinical Training and Programming, including across time zones, cultures and languages
Develop and implement a Global Clinical Training and Programming strategy that is sustainable for continued growth
Coordinate logistics such as creating virtual events platforms, finding clinical providers, ensuring materials are prepared, tracking reporting and evaluation metrics
Work closely with large Jumbo customers to consult on Training and Programming planning, including partnering with internal stakeholders to consult, manage and advise customers
Work closely with the Global team regarding strategy and implementation
Partner with US Program Managers to plan and coordinate training and programming
Ensure we are measuring training and program effectiveness
If possible, involved in some delivery and/or producing of events
Will take a leadership role in planning for global programming related to events such as World Mental Health Day

Fulltime

New

Senior Program Manager, Global Clinical Training and Programming

Reporting to the Director of Clinical Training, the Senior Program Manager, Clin...

Location

India , Mumbai

Salary:

2301600.00 - 2646840.00 INR / Year

Spring Health

Expiration Date

Until further notice

Requirements

Clinical license or equivalent in your country
3-5 years of experience in facilitation and event planning
Complete knowledge and understanding of the unique global challenges, potential solutions, and Clinical Training and Programming
Complete knowledge of Program Management and data evaluation
Complete knowledge of Google Suite, Zoom, and additional events platforms as needed
Solid understanding of instructional design and content development, including strong working knowledge of Adult Learning Principals
Knowledgeable about training evaluation techniques
Communicate effectively with customers and fellow Spring team members

Job Responsibility

Serve as the primary Project Manager for Global (Non US) Clinical Training and Programming
Serve as a SME on Global Clinical Training and Programming, including across time zones, cultures and languages
Develop and implement a Global Clinical Training and Programming strategy that is sustainable for continued growth
Coordinate logistics such as creating virtual events platforms, finding clinical providers, ensuring materials are prepared, tracking reporting and evaluation metrics
Work closely with large Jumbo customers to consult on Training and Programming planning, including partnering with internal stakeholders to consult, manage and advise customers
Work closely with the Global team regarding strategy and implementation
Partner with US Program Managers to plan and coordinate training and programming
Ensure we are measuring training and program effectiveness
If possible, involved in some delivery and/or producing of events
Will take a leadership role in planning for global programming related to events such as World Mental Health Day

Fulltime

New

Biostatistical Programming Senior Manager

In this vital role you will be responsible for developing and leading teams in t...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
Master’s degree and 8 to 10 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
Bachelor’s degree and 10 to 14 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
Diploma and 14 to 18 years of Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
At least eight (8) years of relevant statistical programming, systems engineering or application programming experience in a clinical development or life sciences setting
Managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources in a statistical programming team working with real-world healthcare data (RWD)
Experience leading a statistical programming team within RWE
RWE generation in pharmaceutical or related research industries, or statistical programming for clinical trials
Training or experience using the Observational Medical Outcomes Partnership (OMOP) common data model
Department or multi-team management

Job Responsibility

Provide technical solutions to programming problems within the Centre for Observational Research (CfOR)
Lead and develop technical programming and process improvement initiatives within CfOR
Represent the programming function and participate in multidisciplinary project team meetings
Project manage programming activities, according to agreed resource and timeline plans
Ensure programming activities adhere to departmental standards and SOPs
Write and/or review and approve programming plans
Write and/or review and approve analysis dataset specifications
Review and approve key study-related documents produced by other functions, e.g. SAPs, CRF, Data Management Plan, etc.
Write, test and validate software programs in Unix to produce analysis datasets and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications
Write, test, validate and execute department-, product- and protocol-level macros and utilities

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Enterprise Resilience Senior Specialist

As our Enterprise Resilience Senior Analyst, you'll be a seasoned expert leading...

Location

United States , Englewood

Salary:

41.14 - 61.20 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Bachelor's Degree, 4 to 6 years of applicable work related experience may be considered
Minimum five (5) years’ experience in Business Continuity, Cyber Resilience, and Disaster Recovery
Minimum three (3-5) years leading large-scale crisis and resilience programs and initiatives

Job Responsibility

Design, manage, and execute a comprehensive training and exercise program (tabletops, drills, functional and full-scale exercises) and lead after-action reviews to validate capabilities, identify gaps, drive remediation, and build system-wide response proficiency
Lead the enterprise business continuity program by planning, developing, and managing global risk, intelligence, and business continuity initiatives to ensure system‑level preparedness, response, and recovery capabilities are designed, implemented, and continuously improved
Serve as the senior subject matter expert and trusted advisor to executive leadership, clinical and operational leaders, cybersecurity, legal, and communications teams
provide guidance before, during, and after incidents and, when needed, act as incident commander, incident manager, or senior advisor to enable timely, coordinated decision-making and recovery
Coordinate cross-functional preparedness and resilience efforts across clinical, IT/cybersecurity, facilities, logistics, communications and other stakeholders, and advise on risk mitigation strategies, policies, processes, and technology improvements to reduce disruption impact
Establish metrics, reporting, and governance for resilience and business continuity planning
prepare briefings for senior leadership and governance committees and track corrective actions to closure to ensure continuous improvement and accountability
Maintain external partnerships and regulatory and industry awareness—public health, emergency management, regional healthcare coalitions, law enforcement, and vendors—and ensure all business continuity activities comply with organizational, legal, privacy, and security requirements

What we offer

medical, prescription drug, dental, vision plans, life insurance, paid time off (full-time benefit eligible team members may receive a minimum of 14 paid time off days, including holidays annually), tuition reimbursement, retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

Clinical Quality Compliance Senior Manager

The role provides proactive end to end quality support for the development and i...

Location

Türkiye , Istanbul

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of Quality Management, Quality Assurance and Good Clinical Practices experience in the pharmaceutical/biotech industry where risk-based quality management and quality by design are a core responsibility
Master’s degree and 4 years of the previous mentioned experience
Bachelor’s degree and 6 years of the previous mentioned experience
Associate’s degree and 10 years of the previous mentioned experience
Oversight and implementation of Quality Management Systems and experience managing quality in electronic QMS such as Veeva or Track wise
Thorough understanding of Clinical R&D activities and Global Regulations
Experience with Regulatory Submission and Inspection Management procedures
Quality Oversight of Clinical Trials, including clinical trial protocol development, execution, and submissions
Leadership or mentoring experience is ideal, in a regional capacity would be phenomenal
Excellent verbal and written communication skills, including strong business writing abilities and active listening

Job Responsibility

Act as a Good Clinical Practice (GCP) Subject Matter Expert, offering independent, objective quality guidance
Oversee quality across all clinical development stages
Plan and execute risk-based GCP audits (sites, affiliates, vendors, studies)
Support regulatory inspections and guide responses, including root cause analysis and CAPAs
Lead quality oversight of Risk Assessment Categorization Tools (RACT) for each trial
Facilitate monthly quality risk reviews with clinical program leaders
Manage audit findings, deviations, and CAPA responses
Ensure regional compliance with local regulations and support vendor evaluations
Analyze data quality trends, identify gaps, and implement corrective actions
Oversee technologies for endpoint data collection (e.g., biomarkers, imaging)

What we offer

Vast opportunities to learn, develop, and move up and across our global organization
Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act
Generous Amgen Total Rewards Plan comprising healthcare, finance, wealth and career benefits
Flexible work arrangements

Vice President, AI Enablement

The Vice President, AI Enablement leads Parexel’s enterprise‑wide Artificial Int...

Location

United States , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

15+ years in data science, AI/ML, or technology leadership roles
at least 7 years in executive or senior leadership
Deep knowledge of clinical research processes, clinical data lifecycle, and pharmaceutical/life sciences regulatory expectations
Experience implementing enterprise AI platforms (GenAI, MLOps, data pipelines, automation)
Proven success operationalizing large-scale AI programs in GxP or other highly regulated industries
Familiarity with emerging AI regulations (EU AI Act, FDA, EMA expectations)
Experience with cloud-based AI ecosystems (Azure preferred)
Master’s degree or PhD in Computer Science, Data Science, Engineering, Bioinformatics, or related field preferred
Advanced business qualifications (MBA or equivalent) desirable
Excellent written and verbal communication skills

Job Responsibility

Define and evolve Parexel’s enterprise AI strategy, roadmap, and investment portfolio
Identify priority use cases aligned to business value, feasibility, and regulatory constraints
Conduct AI maturity assessments and establish long‑term capability-building plans
Co-chair AI governance
Define standards for model lifecycle management, validation, auditability, and transparency
Ensure compliance with GxP, global regulatory guidance, and responsible AI principles
Partner with Quality, Legal, and Compliance to operationalize risk management for AI systems
Oversee enterprise AI platforms, tooling, and data pipelines
Drive scalable architecture for GenAI, ML operations, retrieval‑augmented generation, and secure model hosting
Evaluate and integrate vendor platforms while ensuring data privacy and clinical-grade security

What we offer

Health, Vision & Dental Insurance
Tuition Reimbursement
Vacation/Holiday/Sick Time
Flexible Spending & Health Savings Accounts
Work/Life Balance
401(k) with Company match
Pet Insurance
Opportunity to work on innovative projects at the forefront of the industry
Collaborative and inclusive work environment that values your expertise
Professional advancement and development opportunities

Fulltime

New

Senior Manager, Clinical Marketing – Emerging Procedures

The Senior Manager, Clinical Marketing is responsible for defining and executing...

Location

United States , Austin

Salary:

Not provided

FOCAL ONE

Expiration Date

Until further notice

Requirements

Strong cross-functional experience working across Clinical, Sales, Marketing, and medical teams within healthcare or medical technology environments
Solid understanding of procedural medicine workflows and clinical environments
Proven ability to position and communicate the clinical and patient value of advanced procedures
Comfort with data-driven storytelling using clinical outcomes and peer-reviewed evidence
High attention to detail, quality, and compliance with company and regulatory standards
Demonstrated capability to manage multiple concurrent projects in a complex, matrixed organization
Fluent in English
Excellent communication, presentation, project management and negotiation skills with the ability to influence decision-makers and stakeholders at all levels
Adaptable and able to thrive in a fast-paced environment with a continuous improvement mindset
Proven leader who enjoys building and managing a high performing team

Job Responsibility

Develop and execute emerging procedure strategy
Lead the development of procedure-specific clinical marketing strategies
Translate strategy into actionable annual and quarterly execution plans
Operationalize global initiatives such as KOL development, clinical value definition, and economic value framing
Identify and cultivate surgeon champions and potential key opinion leaders
Support peer-to-peer education models including live case observations, proctoring, and early adopter programs
Develop structured adoption pathways including centers of excellence, early adopter sites, and local or regional workshops
Manage Focal One’s clinical marketing presence at key specialty society meetings and academic conferences
Plan and execute symposia, peer-to-peer courses, and live or recorded procedural education programs
Collaborate with specialty societies and academic partners to support clinical awareness, alignment, and consensus development

Fulltime

Senior Physician, Patient Safety

Join our dynamic Patient Safety team as a Senior Physician where you'll leverage...

Location

United States; Canada , Remote; Alberta

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Good knowledge of drug safety and the drug development process
Good knowledge/understanding of medical terminology
Relevant experience in pharmacovigilance/ Drug Safety/ Clinical Practice
3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required
US Board Certification/board eligibility or regional equivalent for Canada
Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School
Completion of at least basic training in clinical medicine (residency, internship etc.)
Demonstrated success in technical proficiency and scientific creativity
Good presentation and verbal/written communication skills

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs
as applicable) and liaising with the client, as require
Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality
Review appropriateness of medical content in narrative for medical coherence
Assessing seriousness, listedness / expectedness of reported events
Providing medical inputs to case processing team
Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional)
Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative

What we offer

Flexible approach to work that meets your personal needs
Work from home
Benefits vary by country
Investment in your professional and personal development

Senior Program Manager, Global Clinical Training and Programming

Spring Health

Location:
Singapore

Category:
Human Resources

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 18, 2026

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