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Operations Lead For Patient Access
Company | Bristol Myers Squibb |
Address | Princeton, NJ, United States |
Employment type | FULL_TIME |
Salary | |
Category | Pharmaceutical Manufacturing |
Expires | 2023-06-22 |
Posted at | 11 months ago |
Working with Us
- Drives the creation and oversees the support of creating patient access asset level plans.
- Supports Head of Pre-Approval Access / Patient Access and contributes to provide coordination and management of the Post Study Drug (PSD) and other Patient Access programs.
- Uses expert judgment to make sound decisions based on a balanced evaluation of available information within a complex environment of competing project priorities.
- Proactively partners with cross functional counterparts to address issues/concerns.
- Drives compliance with standards of the Post Study Drug Program and Patient Access procedures. Leads and contributes to the execution of operational support for patient access on a global basis.
- Maintains management of patient access programs as needed, via effective matrix management. Works closely with staff supporting staff patient access programs.
- Responsible the training of Study Team in Post Study Access processes and governance.
- Identifies improvement opportunities and brings forward best practices to support patient access
- Role includes providing operational oversight, leadership and execution for patient access programs included but not limited to PAA and PSD and supporting overall patient access programs as needed.
- Serve as a Post Study Drug and Patient Access process SME for GDO and key functions across Medical, Commercial, Clinical, Regulatory, Drug Supply and Patient Safety.
- Drives issues to resolution and communicates to ensure that issues have been worked through to resolution.
- Has strong oral and written communication skills to influence, inform, and guide global operational teams.
- Frequently communicates program status to internal and external stakeholders, including Sr. Leadership.
- Proven change management skills and the ability to lead partnerships across projects and multidisciplinary teams.
- Demonstrates diplomacy and/or acts as primary point of escalation when interfacing with other functional areas, clinical research organizations (CROs) and other outside vendors.
- BA/BS or equivalent degree work experience.
- Candidate should have a minimum of ten years’ experience in Clinical Operations and ideally would have experience in managing Pre-Approval Access, Compassionate Use or Managed / Expanded Access programs.
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