Manager, Portfolio Operations, Medical Evidence Generation, Managed Access Programs, & Real-World Evidence - Global Medical (multiple openings)
Key Skills for This Role
Full Job Posting
Responsibilities
- Study Systems & Documentation Excellence
- Owns portfolio-wide eTMF oversight, quality, completeness, and inspection readiness.
- Drives periodic eTMF health reviews and remediation activities.
- Establishes standards, metrics, and KPIs for document compliance.
- Ensures consistent document management practices across all studies.
- CTMS & Operational Data Management
- Manages CTMS processes and data quality
- Monitors study records, milestone accuracy, and portfolio reporting
- Implements governance for system usage and compliance
- Supports system enhancements, training, issue resolution
- Financial Operations
- Manages centralized invoice processing and reconciliation activities
- Oversees purchase order creation, tracking, and lifecycle management
- Ensures compliance with procurement and financial controls
- Supports budget tracking and accrual monitoring
- Study Closure & Archive Support Services
- Follows standardized closure and archival processes
- Coordinates documentation readiness for closed studies
- Monitors closure milestones and archive compliance
- Partners with GTLs/GTAs to support timely study closeout
- Operational Process Excellence
- Creates and maintains standardized tools, templates, checklists, and workflows
- Harmonizes operational practices across therapeutic areas
- Identifies efficiency opportunities and automation solutions
- Establishes consistent service delivery models across the portfolio
- Compliance & Inspection Readiness
- Monitors operational compliance metrics across studies
- Coordinates remediation activities for recurring operational issues
Qualifications
- BA/BS or equivalent degree in relevant discipline.
- Manager level: minimum 3-5 years of experience in clinical/medical trial operations, systems administration (eTMF/CTMS), financial operations, or related pharmaceutical/healthcare industry experience.
- Experience with eTMF and CTMS systems required.
- Experience with purchase order management, invoice processing, or financial administration in a clinical/medical trials environment preferred.
- Strong understanding of GCP/ICH guidelines, document management standards, and inspection readiness requirements.
- Excellent organizational skills with strong attention to detail.
- Ability to manage multiple studies and therapeutic areas simultaneously and prioritize competing demands.
- Strong communication and stakeholder management skills, with the ability to partner effectively with cross-functional partners.
- Experience driving process standardization or continuous improvement initiatives preferred.
- Travel requirement of up to 5%.
- #LI-HYBRID
- We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.
- How We Work
- Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.
- Supporting People with Disabilities
- BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
- Candidate Rights
- BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
- For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
- Data Protection
- We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
- Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
- If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.
- R1607302: Manager, Portfolio Operations, Medical Evidence Generation, Managed Access Programs, & Real-World Evidence - Global Medical (multiple openings)
Preferred Qualifications
- Experience with purchase order management, invoice processing, or financial administration in a clinical/medical trials environment preferred.
- Experience driving process standardization or continuous improvement initiatives preferred.
About Bristol Myers Squibb
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