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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
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 Responsibilities

Clinical 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
Key Requirements
  • 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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