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Senior Manager, Clinical Partner Outsourcing | Clinical Procurement | Contract & Supplier Management | R&D Clinical
Job in
Everett, Middlesex County, Massachusetts, 02149, USA
Listed on 2026-08-06
Listing for:
SoTalent
Contract
position Listed on 2026-08-06
Job specializations:
-
Business
Regulatory Compliance Specialist
Job Description & How to Apply Below
Senior Manager, Clinical Partner Outsourcing
Role Overview
Senior-level role within a global R&D clinical operations environment. Responsible for clinical study outsourcing, supplier contracts, and commercial governance. Ensures timely study delivery with strong financial discipline and compliance. Works cross-functionally across clinical operations, procurement, and study teams. Hybrid / remote flexibility depending on location (Cambridge, MA base).
Key ResponsibilitiesClinical Contracts & Outsourcing
- Develop and finalise study-level contracts and change orders aligned to Master Service Agreements
- Lead commercial structuring, contracting, and supplier negotiations across CROs and vendors
- Translate clinical study requirements into robust commercial agreements
- Manage contract amendments throughout the study lifecycle
- Support study closeout and final financial reconciliation
Financial & Commercial Management
- Build and validate cost models and pricing assumptions for clinical studies
- Generate cost estimates to support study planning and budgeting
- Ensure fiscal discipline across outsourced clinical operations
- Oversee alignment between contractual terms and operational execution
Supplier & Stakeholder Management
- Drive negotiations with CROs and clinical suppliers to optimise commercial terms
- Resolve operational and contractual issues in collaboration with study teams
- Escalate risks and manage contingency planning where required
- Maintain strong relationships with internal and external stakeholders
Governance, Compliance & Process Improvement
- Ensure compliance with internal policies, GCP, ICH guidelines, and regulatory standards
- Support inspection readiness for regulated clinical activities
- Identify industry best practices through benchmarking and continuous improvement
- Lead or support strategic initiatives and operational improvements
- Bachelor's degree required (advanced degree such as MBA preferred)
- 7+ years' experience in pharmaceutical, clinical research, or R&D outsourcing
- Strong background in clinical procurement, supplier management, or contract negotiation
- Deep understanding of clinical trial processes and regulatory frameworks
- Experience with CRO models, clinical budgets, and commercial structures
- Strong financial analysis and cost modelling capability
- Knowledge of GCP and ICH guidelines
- Excellent stakeholder management and communication skills
- Strong strategic thinking and project management ability
Work Environment
- Global pharmaceutical R&D organisation
- High-complexity clinical trial outsourcing and procurement environment
- Cross-functional collaboration across clinical operations, finance, and vendors
- Strong regulatory and compliance-driven structure
- Fast-paced, multi-study portfolio management environment
Position Requirements
10+ Years
work experience
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