Amgen is hiring for the position of Clinical Pricing & Payment Sr Associate under its Clinical Development career category. The role is based in Hyderabad, India, and involves supporting clinical study pricing, site budget preparation, payment configuration, site contracting, invoice approvals, payment reconciliation, and clinical trial payment operations.
Candidates in clinical trial operations, clinical study start-up, site contracting, clinical finance, and payment administration can review the job responsibilities and apply through Amgen’s official careers portal.
Job Details
| Particulars | Details |
|---|---|
| Company | Amgen |
| Job Title | Clinical Pricing & Payment Sr Associate |
| Job Requisition ID | R-260941 |
| Career Category | Clinical Development |
| GCF Level | 4 |
| Job Location | Hyderabad, India |
| Work Mode | On-site |
| Employment Type | Full-time |
| Job Posted | November 6, 2026 |
| Application Mode | Online |
Position
Clinical Pricing & Payment Sr Associate – Clinical Development
The selected candidate will support clinical study pricing and payment activities, including country and site budget preparation, Clinical Trial Payment System (CTPS) configuration, invoice processing, payment reconciliation, and coordination with cross-functional clinical research teams.
Key Responsibilities
1. Clinical Study Pricing and Budget Management
- Support the Pricing Manager with study budget design and initial budget finalization.
- Coordinate Budget Strategy and Kick-Off meetings.
- Prepare country budget worksheets and supporting documentation.
- Maintain finalized and negotiated site budgets and study-specific pricing trackers.
2. Clinical Trial Payment Operations
- Complete study-level payment set-up activities, including payment triggers and budget mapping.
- Configure clinical trial payment systems and prepare payment documentation.
- Review and approve site invoices and manual payment requests.
- Prepare monthly site payment and split-payee allocation information.
- Perform payment reconciliation and site close-out activities.
3. Clinical Trial Payment System (CTPS)
- Create and maintain site configuration packages within CTPS.
- Process initial configurations and change requests arising from finalized site budgets, contracts, or protocol amendments.
- Manage assigned CTPS user access requests.
- Investigate payment and system-related queries.
4. Site Contracting and Coordination
- Provide operational and administrative support for site contracting activities.
- Maintain site contracting information within applicable systems and workflows.
- Coordinate with Study Start-Up, Clinical Study Teams, Finance, Data Management, and Site Management.
- Support contract-related activities arising from protocol or site budget amendments.
5. Quality Checks and Reporting
- Validate site budget and payment information for accuracy and completeness.
- Investigate and escalate payment discrepancies.
- Prepare pricing and payment status reports and operational metrics.
- Track activities, dependencies, risks, and issues that could affect study start-up, site activation, or payment execution.
6. Continuous Improvement
- Identify opportunities to simplify, standardize, and automate operational activities.
- Develop and share templates, tools, and best practices.
- Support CAPA implementation and process-improvement initiatives.
- Participate in cross-functional projects and departmental activities.
Required Skills and Functional Knowledge
The responsibilities outlined in the job description involve the following functional areas:
- Clinical study pricing and budget management.
- Country and site budget preparation.
- Clinical trial payment operations.
- Clinical Trial Payment System (CTPS) configuration.
- Site invoice review and payment processing.
- Payment reconciliation and split-payee allocation.
- Site contracting administration.
- Data validation and quality checks.
- Clinical study start-up coordination.
- Cross-functional stakeholder coordination.
- Operational reporting and process improvement.
