Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Bristol Myers Squibb

Manager, Portfolio Operations, Medical Evidence Generation, Managed Access Programs, Real-World Evidence – Global Medical

Bristol Myers Squibb

. Provide centralized operational support, systems oversight, compliance execution, and administrative services across the MEG Operations team and portfolio .

Posted 10/23/2026full-timeHyderabad • IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in eTMF and CTMS systems administration, ensuring compliance with GCP/ICH guidelines and document management standards. Proven ability to manage financial operations, including purchase order management and invoice processing, while driving process standardization and operational efficiency.

Highest-signal resume keywords
ETMF OversightCTMS ManagementFinancial AdministrationGCP/ICH ComplianceProcess Standardization

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
ETMF SystemsCTMS SystemsPurchase Order ManagementInvoice ProcessingDocument ManagementQuality AssuranceData Quality ManagementBudget TrackingAccrual MonitoringOperational Compliance Metrics
Soft Skills
Organizational SkillsAttention to DetailCommunication SkillsStakeholder ManagementCross-Functional Collaboration
Industry Keywords
Clinical TrialsMedical TrialsPharmaceutical IndustryHealthcare IndustryOperational Support

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Provide centralized operational support, systems oversight, compliance execution, and administrative services across the MEG Operations team and portfolio
  • Serve as the central point of accountability for eTMF, CTMS, financial administration, purchase order management, invoice processing, and study documentation oversight
  • Own portfolio-wide eTMF oversight, quality, completeness, and inspection readiness
  • Drive periodic eTMF health reviews and remediation activities
  • Establish standards, metrics, and KPIs for document compliance
  • Ensure consistent document management practices across all studies
  • Manage CTMS processes and data quality
  • Monitor study records, milestone accuracy, and portfolio reporting
  • Implement governance for system usage and compliance
  • Support system enhancements, training, and issue resolution
  • Manage centralized invoice processing and reconciliation activities
  • Oversee purchase order creation, tracking, and lifecycle management
  • Ensure compliance with procurement and financial controls
  • Support budget tracking and accrual monitoring
  • Follow standardized study closure and archival processes
  • Coordinate documentation readiness for closed studies
  • Monitor closure milestones and archive compliance
  • Partner with GTLs/GTAs to support timely study closeout
  • Create and maintain standardized tools, templates, checklists, and workflows
  • Harmonize operational practices across therapeutic areas
  • Identify efficiency opportunities and automation solutions
  • Establish consistent service delivery models across the portfolio
  • Monitor operational compliance metrics across studies
  • Coordinate remediation activities for recurring operational issues
  • Report to the Senior Director, Business Operations Lead, MEG Operations

Requirements

What you’ll need
  • BA/BS or equivalent degree in relevant discipline
  • 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%

Benefits

Comp & perks
  • Opportunities for growth
  • Supportive environment
  • Inclusion
  • Wellbeing
  • Flexibility
  • Comprehensive benefits
  • Reasonable workplace accommodations/adjustments
  • Ongoing support in roles